Buy 5F-ADB Powder Canada , Order 5F-ADB for sale British Columbia , Where to purchase research chemical online Alberta, Research chemical vendor Manitoba

Buy 5F-ADB Powder (additionally referred to as 5F-MDMB-PINACA) is an indazole-primarily based totally artificial cannabinoid from the indazole-3-carboxamide family, which has been used as an energetic component in artificial hashish merchandise and has been offered on line as a clothier drug. 5F-ADB is a strong agonist of the CB1 receptor, aleven though it’s miles uncertain whether or not it’s miles selective for this target. 5F-ADB changed into first diagnosed in November 2014 from autopsy samples taken from an character who had died after the use of a product containing this substance. Subsequent trying out diagnosed 5F-ADB to had been found in a complete of ten folks who had died from unexplained drug overdoses in Japan among September 2014 and December 2014. 5F-ADB is thought to be extraordinarily strong primarily based totally at the very low ranges detected in tissue samples, and looks to be drastically greater poisonous than in advance artificial cannabinoid tablets that had formerly been offered.

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In 2018, 5F-ADB changed into the maximum not unusualplace artificial cannabinoid to be diagnosed in Drug Enforcement Administration seizures. 5F-ADB changed into additionally diagnosed in cannabidiol (CBD) merchandise from a US-primarily based totally CBD producer in 2018. Man-made cannabinoids have a tendency to be fairly new chemical compounds of mistreatment. A brief even as ago, mistreatment of human-made cannabinoids remains an increasing number of documented withinside the mass media and health-associated books. In the occasion that new chemical materials are announced, their precise utilization is at the start now no longer limited with the aid of using prohibition for that reason everyday remedy assessments can’t verify their precise utilization.

The precise utilization of those varieties of chemical materials amongst teens and the more youthful era is constantly expanding, which makes it very essential to surprising emergency offerings continually to be familiar with the indicators and symptoms and symptoms and signs of inebriation present. Overdose and continual usage of those varieties of chemical compounds should probably reason uncomfortable facet consequences which consist of altered mental position, tachycardia, and lack of intelligence. Many organizations withinside the USA reported, six times of intense inebriation with the aid of using human-made cannabinoids 5F-ADB in addition to MMB-2201 along side logical confirmation.

Chemical and bodily data
Formula: C20H28FN3O3

Molar mass: 377.460 g·mol?1

Research chemical vendor New Brunswick

Legal status
In the United States, 5F-ADB is a time table I managed substance

See additionally
5F-AB-PINACA
5F-AMB
5F-APINACA
AB-CHMINACA
AB-FUBINACA
AB-CHFUPYCA
AB-PINACA
ADB-CHMINACA
ADB-FUBINACA
ADB-PINACA
ADBICA
APICA
APINACA
MDMB-CHMICA
MDMB-FUBINACA
PX-3

5F-NNE1 is not approved for use as a treatment, or with humans or animals in any way. Do not consume the substance, and do not let it be handled by anyone other than trained professionals – Buy 5F-MN24 Powder..

Chemical and physical data
Formula: C24H23FN2O

Molar mass: 374.459 g·mol?1

See also
5F-ADBICA
5F-SDB-006
AM-2201
FDU-NNE1
FUB-144
MMB-2201
NNE1
PX-1

Buy 5F-PCN Powder Alberta , 5F-PCN Powder for sale online Canada , Where to purchase Research chemical in Calgary , Purchase 5F-PCN Edmonton

Buy 5F-PCN Powder (also known as 5F-MN-21) is an azaindole-based synthetic cannabinoid that is presumed to be a potent agonist of the CB1 receptor and has been sold online as a designer drug. It is closely related to NNE1. Given the known metabolic liberation (and presence as an impurity) of amantadine in the related compound APINACA, it is suspected that metabolic hydrolysis of the amide group of 5F-PCN may release 1-naphthylamine, a known carcinogen.

5F-MN-21 is also a designer drug with pronounced physiological and psychoactive effects.D The toxicological and physiological properties of 5F-PCN are not known. Synthetic cannabinoids like 5F-PCN might display high affinity for peripheral CB1 and CB2 cannabinoid receptors.

The toxicological and physiological properties of 5F-PCN are not known. Synthetic cannabinoids like 5F-PCN might display high affinity for peripheral CB1 and CB2 cannabinoid receptors.

1-(5-Fluoro-pentyl)-1H-pyrrolo[3,2-c]pyridine-3-carboxylic acid naphthalen-1-ylamide and all other designer drugs sold on this website are intended for research and forensic applications.

What does “powder” form mean & why it matters | Order Research chemical Canada

• The “powder” or crystalline form refers to the unformulated active compound in solid form (often as a crystalline or fine powder).

• In research or analytical laboratories, this form allows measurement, purity checks, structural analysis, etc.

• In illicit or unregulated contexts, powder form is risky because:

  1. Dosage is difficult to control. Even small errors can lead to unexpectedly strong effects.

  2. Impurities or adulterants may be present.

  3. There may be mislabeling or confusion with other synthetic cannabinoids.

Please store this synthetic cannabinoid in a cool and dry place. Stability of the cannabinoid compound 5F-PCN up to 2 years under correct storage conditions.

Legal status
Sweden’s public health agency suggested to classify 5F-PCN as hazardous substance on November 10, 2014.

Chemical and physical data
Formula: C23H22FN3O

Molar mass: 375.4 g/mol g·mol?1

Pharmacology & Effects (what is known / expected)

• As a synthetic cannabinoid agonist at CB₁, 5F-PCN is presumed to produce cannabinoid-like effects: altered perception, psychoactive “high,” possible relaxation or euphoria. Because it’s “full agonist” (or presumed potent), the effects may be stronger and more unpredictable than natural THC. UNODC+1

• There is very limited data on human pharmacokinetics (onset, duration, metabolism), side effect profile, or dose ranges. Most knowledge is from structural analogues and early-warning / forensic reports.

The code number SDB-005 was originally used for a different compound, the N-phenyl instead of N-benzyl analogue of SDB-006. This compound is a potent agonist of the CB1 receptor (Ki = 21 nM) and CB2 receptor (Ki = 140 nM).

However, SDB-005 was subsequently used as the name for the indazole-3-carboxylate compound mentioned above when it was sold in Europe as a designer drug, and was entered into the EMCDDA synthetic drug database under this name. Consequently, there are now two distinct, yet fairly closely related cannabinoid compounds, which may both be referred to under the code SDB-005.

Technical Information
Formal Name: naphthalen-1-yl 1-(5-fluoropentyl)-1H-indazole-3-carboxylate
Molecular Formula: C23H21FN2O2
Formula Weight: 376.4
Purity: ?98%
Formulation: A crystalline solid
?max: 221, 302 nm
SMILES: O=C(OC1=C(C=CC=C2)C2=CC=C1)C3=NN(CCCCCF)C4=CC=CC=C43
InChi CodeInChI=1S/C23H21FN2O2/c24-15-6-1-7-16-26-20-13-5-4-12-19(20)22(25-26)23(27)28-21-14-8-10-17-9-2-3-11-18(17)21/h2-5,8-14H,1,6-7,15-16H2
InChi Key: FNMFGMMHNFDPNT-UHFFFAOYSA-N
Shipping & Storage Information
Storage: -20°C
Shipping: Room Temperature in continental US; may vary elsewhere
Stability: ? 2 years
WARNING This product is not for human or veterinary use.

Pharmacology
5F-PB-22 acts as a full agonist with a binding affinity of 0.468 nM at CB1 and 0.633 nM at CB2 cannabinoid receptors.

Legal status
As of October 2015 5F-PB-22 is a controlled substance in China.

In January 2014, 5F-PB-22 was designated as a Schedule I controlled substance in the United States after several deaths were associated with its use.

In the United Kingdom, 5F-PB-22 is now classified and controlled as a Class B drug, following the November 2016 amendment to the Misuse of Drugs Act 1971. Several other synthetic cannabinoids structurally related to JWH-018, like 5F-PB-22, were also classified in this amendment.

Chemical and physical data
Formula: C23H21FN2O2

Molar mass: 376.431 g·mol?1

Purity ?98%
Formulation A neat solid
SMILES O=C(OC1=C(N=CC=C2)C2=CC=C1)C3=CN(CCCCCF)C4=C3C=CC=C4
InChI Code InChI=1S/C23H21FN2O2/c24-13-4-1-5-15-26-16-19(18-10-2-3-11-20(18)26)23(27)28-21-12-6-8-17-9-7-14-25-22(17)21/h2-3,6-12,14,16H,1,4-5,13,15H2
InChI Key

MBOCMBFDYVSGLJ-UHFFFAOYSA-N

Technical Information
Formal Name 1-(5-fluoropentyl)-8-quinolinyl ester-1H-indole-3-carboxylic acid
CAS Number 1400742-41-7
Synonyms

5-fluoro QUPIC

See also
AM-2201
JWH-018
QUCHIC
QUPIC
SDB-001
SDB-005

The (S)-enantiomer of ADB-FUBINACA is described in a 2009 Pfizer patent and has been reported to be a potent agonist of the CB1 receptor and the CB2 receptor with EC50 values of 1.2 nM and 3.5 nM, respectively. ADB-FUBINACA features a carboxamide group at the 3-indazole position, like SDB-001 and STS-135. ADB-FUBINACA appears to be the product of rational drug design, since it differs from AB-FUBINACA only by the replacement of the isopropyl group with a tert-butyl group.

An analogue of ADB-FUBINACA, ADSB-FUB-187, containing a more functionalized carboxamide substituent was recently reported.

Technical Information Formal Name: N-[1-(aminocarbonyl)-2,2-dimethylpropyl]-1-[(4-fluorophenyl)methyl]-1H-indazole-3-carboxamide CAS Number: 1445583-51-6 Molecular Formula: C21H23FN4O2 Formula Weight: 382.4 Purity: ?98% Formulation: A neat solid SMILES: O=C(NC(C(N)=O)C(C)(C)C)C1=NN(CC2=CC=C(F)C=C2)C3=C1C=CC=C3 InChi CodeInChI=1S/C21H23FN4O2/c1-21(2,3)18(19(23)27)24-20(28)17-15-6-4-5-7-16(15)26(25-17)12-13-8-10-14(22)11-9-13/h4-11,18H,12H2,1-3H3,(H2,23,27)(H,24,28) InChi Key: ZSSGCSINPVBLQD-UHFFFAOYSA-N DEA Schedule: I Shipping & Storage Information Storage: -20°C Shipping: Room Temperature in continental US; may vary elsewhere Stability: ? 3 years Legality In the United States, ADB-FUBINACA is a Schedule I controlled substance.

Metabolism Twenty-three ADB-FUBINACA major metabolites were identified in several incubations with cryopreserved human hepatocytes. Major metabolic pathways were alkyl and indazole hydroxylation, terminal amide hydrolysis, subsequent glucuronide conjugations, and dehydrogenation

Side effects One death through coronary arterial thrombosis has been linked to ADB-FUBINACA intoxication.

At least an additional 8 deaths in Hungary in 2015 are linked to the usage of this material, all deaths were youngsters below 21.

WARNING This product is not for human or veterinary use.

Safe shipping to USA, Germany, France,Poland, EU, UK and other countries. So if you are looking to buy FAB-144 or other related products then you are at the right place.

FAB-144 is an analogue of XLR-11, which acts like a potent agonist for the cannbinoid receptors. The CB1 and CB2 receptors offer a Ki of 24.2nM along with an EC50 of 359nM at CB1.

To purchase FAB-144 from us, you must be at least 18 years of age and you must also be in full legal compliance with the research chemical laws of your nation. Our FAB-144 is not intended for human or animal use. It is only designed for laboratory use and research experiments-Buy FAB-144 Powder Online.

Experimental findings for FAB-144 typically include increased appetite, stimulation, energy, perceiving reality as a dream-like state, relaxation, elevated mood, and other findings that are similar to other synthetic cannabinoids.

Legal status
Sweden’s public health agency suggested classifying FAB-144 as hazardous substance on November 10, 2014.

Technical Information
Formal Name(1-(5-fluoropentyl)-1H-indazol-3-yl)(2,2,3,3-tetramethylcyclopropyl)methanone
Purity: ?98%
Formulation: A solution in methanol
?max: 208, 247, 241, 307 nm
SMILES: FCCCCCN1N=C(C(C2C(C)(C)C2(C)C)=O)C3=C1C=CC=C3
InChi CodeInChI=1S/C20H27FN2O/c1-19(2)18(20(19,3)4)17(24)16-14-10-6-7-11-15(14)23(22-16)13-9-5-8-12-21/h6-7,10-11,18H,5,8-9,12-13H2,1-4H3
InChi Key: LVJQJRUAYXVEGN-UHFFFAOYSA-N
Chemical and physical data
Formula: C20H27FN2O

Molar mass: 330.4 g/mol g·mol?1

Shipping & Storage Information
Storage: -20°C
Shipping: Room Temperature in continental US; may vary elsewhere
Stability: ? 1 year
WARNING This product is not for human or veterinary use.

See also
JWH-018
STS-135
UR-144

Our CBD isolate is of the purest concentration, non-toxic, and has zero THC. Derived from aerial parts of hemp plants grown and farmed in Colorado, utilizing strict organic farming practices, our isolate products are 99%+ pure CBD. Completely non-synthetic, 100% all-natural, and non-GMO. Our CBD isolate products are lab tested via a third-party laboratory, ensuring purity and quality.

Our CBD isolate is manufactured in a cGMP, EU GMP, & ISO-9001 Certified facility.  Certified for Food & Cosmetic use. 

Our lab also received their API certification, which stands for Active Pharmaceutical Ingredient.  

CBD Isolate can be: dabbed, vaporized, orally ingested, cooked with or combined with and smoked with herbs.

NOTE:  Orders of 1 – 4 grams will be individually packaged in 1g containers.  5 or more grams will packaged in one container unless otherwise specified in the “notes” section on the order page.  There may be a charge for individual gram packaging.  Please email us if you have specific packaging requirements, thank you.

Our CBD isolate is of the purest concentration, non-toxic, and has zero THC. Derived from aerial parts of hemp plants grown and farmed in Colorado, utilizing strict organic farming practices, our isolate products are 99%+ pure CBD. Completely non-synthetic, 100% all-natural, and non-GMO. Our CBD isolate products are lab tested via a third-party laboratory, ensuring purity and quality.

Our CBD isolate is manufactured in a cGMP, EU GMP, & ISO-9001 Certified facility.  Certified for Food & Cosmetic use. 

Our lab also received their API certification, which stands for Active Pharmaceutical Ingredient.  

CBD Isolate can be: dabbed, vaporized, orally ingested, cooked with or combined with and smoked with herbs.

NOTE:  Orders of 1 – 4 grams will be individually packaged in 1g containers.  5 or more grams will packaged in one container unless otherwise specified in the “notes” section on the order page.  There may be a charge for individual gram packaging.  Please email us if you have specific packaging requirements, thank you.

Ingredients: cannabidiol (derived from hemp)

Technical Information
Formal Name: [5-(2-fluorophenyl)-1-pentyl-1H-pyrrol-3-yl]-1-naphthalenyl-methanone
CAS Number: 914458-26-7
Molecular Formula: C26H24FNO
Formula Weight: 385.5
Purity: ?96%
Formulation: A crystalline solid
?max: 217, 250 nm
SMILES: O=C(C1=CN(CCCCC)C(C2=CC=CC=C2F)=C1)C3=C4C(C=CC=C4)=CC=C3
InChi CodeInChI=1S/C26H24FNO/c1-2-3-8-16-28-18-20(17-25(28)23-13-6-7-15-24(23)27)26(29)22-14-9-11-19-10-4-5-12-21(19)22/h4-7,9-15,17-18H,2-3,8,16H2,1H3
InChi Key: WYNZPDDTQGVCLZ-UHFFFAOYSA-N
Shipping & Storage Information
Storage: -20°C
Shipping: Room Temperature in continental US; may vary elsewhere
Stability: ? 1 year

See also
JWH-147
WARNING This product is not for human or veterinary use.

JWH-250 or (1-pentyl-3-(2-methoxyphenylacetyl)indole) is an analgesic chemical from the phenylacetylindole family that acts as a cannabinoid agonist at both the CB1 and CB2 receptors, with a Ki of 11 nM at CB1 and 33 nM at CB2. Unlike many of the older JWH series compounds, this compound does not have a naphthalene ring, instead occupying this position with a 2?-methoxy-phenylacetyl group, making JWH-250 a representative member of a new class of cannabinoid ligands. Other 2?-substituted analogues such as the methyl, chloro and bromo compounds are also active and somewhat more potent.

Buy UR-144 Powder Online
UR-144 has high affinity for the CB2 receptor with a Ki of 1.8 nM but 83x lower affinity for the CB1 receptor with a Ki of Associate in Nursingd fifty} nM. it absolutely was found to possess an EC50 of 421 nM for human CB1 receptors, and seventy two nM for human CB2 receptors. UR-144 produces arrhythmia and physiological state in rats at a dose of ten mg/kg, suggesting weak cannabinoid-like activity.

with chemicals it’s closely concerning alternative 2,2,3,3-tetramethylcyclopropyl artificial cannabinoids like A-796,260 and A-834,735 however with a special substitution on the 1-position of the indole core, in these compounds its 1-pentyl cluster is replaced with alkylheterocycles like 1-(2-morpholinoethyl) and 1-(tetrahydropyran-4-ylmethyl).

Chemical and physical information
Formula: C21H29NO

Molar mass: 311.461 g/mol g·mol?1

Dose
Inhalation (tentative because of an absence of information)

Range: 2.5 to twenty mg
the general public are exposed to the drug within the type of “blends” that contain variable levels of UR-144. It’s not informed use those products.

Timeline
Inhalation (tentative because of an absence of information)
Total: one – two hours
Onset: below ten minutes
see
AB-001
AM-1221
4-HTMPIPO
FAB-144
JTE 7-31
JWH-018
N-(S)-Fenchyl-1-(2-morpholinoethyl)-7-methoxyindole-3-carboxamide
XLR-11

it’s a structural analog of AM-2201 within which the central indole ring has been replaced by indazole.

outline sheet: THJ-2201
THJ-2201 (1-?[(5-?fluoropentyl)-?1H-?indazol-?3-?yl](naphthalen-?1-?yl)methanone) could be a synthetic cannabinoid and analog of AM-2201. it’s been marketed by several analysis chemical vendors as a legal various to the favored AM-2201, which had been prohibited in 2011.

Cannabinoids are unremarkably smoke-dried or vaporized to attain a fast onset of effects and speedy offset. THJ-2201 is orally active once dissolved during a lipid, which may increase the period significantly. Like alternative cannabinoids, it’s insoluble in water however dissolves in plant product and lipids.

not like cannabis, the chronic abuse of artificial cannabinoids has been related to multiple deaths and additional dangerous facet effects and toxicity in general. Therefore, it is powerfully discouraged to require this substance for extended periods of your time or in excessive doses.

medicine
though this substance has not been formally studied, from analysis of the structure, it’s likely that THJ-2201 encompasses a similar binding profile to it of AM-2201 and matches several of the in vivo properties of ?9-THC. like AM-2201, this compound is believed to act as a potent full agonist to the central CB1 and peripheral CB2 receptors with Ki values of 1.0 and 2.6nM respectively. However, the role of those interactions and the way they lead to the cannabinoid high expertise continues to stay elusive.

Subjective effects
the results listed below are primarily based upon the subjective effects index and private experiences of PsychonautWiki contributors. These effects should be soft on a grain of salt and can seldom (if ever) occur all at once, however heavier doses will increase the probabilities of inducement a full vary of effects. Likewise, adverse effects become far more probably on higher doses and will embody serious injury or death.

Chemical and physical knowledge
Formula C23H21FN2O
Molar mass 360.42 g/mol g·mol?1
3D model (JSmol) Interactive

cf
AM-694
AM-1235
AM-2232
AM-2233
FUBIMINA
JWH-018
List of AM cannabinoids
List of JWH cannabinoids
NM-2201
THJ-018

Synthetic cannabinoids are the largest and most structurally diverse class of new psychoactive substances, with manufacturers often using isomerism to evade detection and circumvent legal restriction. The regioisomeric methoxy? and fluorine?substituted analogs of SDB?006 (N?benzyl?1?pentyl?1H?indole?3?carboxamide) were synthesized and could not be differentiated by gas chromatography–mass spectrometry (GC–MS), but were distinguishable by liquid chromatography–quadrupole time?of?flight–MS (LC–QTOF–MS). In a fluorescence?based plate reader membrane potential assay, SDB?006 acted as a potent agonist at human cannabinoid receptors (CB1 EC50 = 19 nM). All methoxy? and fluorine?substituted analogs showed reduced potency compared to SDB?006, although the 2?fluorinated analog (EC50 = 166 nM) was comparable to known synthetic cannabinoid RCS?4 (EC50 = 146 nM). Using biotelemetry in rats, SDB?006 and RCS?4 evoked comparable reduction in body temperature (~0.7°C at a dose of 10 mg/kg), suggesting lower potency than the recent synthetic cannabinoid AB?CHMINACA (>2°C, 3 mg/kg).

Technical Information
Formal Name: 1-pentyl-N-(phenylmethyl)-1H-indole-3-carboxamide
CAS Number: 695213-59-3
Molecular Formula: C21H24N2O
Formula Weight: 320.4
Purity: ?98%
Formulation: A crystalline solid
?max: 218, 291 nm
SMILES: CCCCCN1C=C(C(NCC2=CC=CC=C2)=O)C3=C1C=CC=C3
InChi CodeInChI=1S/C21H24N2O/c1-2-3-9-14-23-16-19(18-12-7-8-13-20(18)23)21(24)22-15-17-10-5-4-6-11-17/h4-8,10-13,16H,2-3,9,14-15H2,1H3,(H,22,24)
InChi Key: OLACYTSBFXCDOH-UHFFFAOYSA-N
Shipping & Storage Information
Storage: -20°C
Shipping: Room Temperature in continental US; may vary elsewhere
Stability: ? 2 years
WARNING This product is not for human or veterinary use.

See also
5F-CUMYL-PINACA
5F-SDB-006
APINACA
CUMYL-PICA
CUMYL-PINACA
CUMYL-THPINACA
SDB-001
SDB-005
STS-135

The code number SDB-005 was originally used for a different compound, the N-phenyl instead of N-benzyl analogue of SDB-006. This compound is a potent agonist of the CB1 receptor (Ki = 21 nM) and CB2 receptor (Ki = 140 nM).

However, SDB-005 was subsequently used as the name for the indazole-3-carboxylate compound mentioned above when it was sold in Europe as a designer drug, and was entered into the EMCDDA synthetic drug database under this name. Consequently, there are now two distinct, yet fairly closely related cannabinoid compounds, which may both be referred to under the code SDB-005.

Technical Information
Formal Name: naphthalen-1-yl 1-pentyl-1H-indazole-3-carboxylate
Molecular Formula: C23H22N2O2
Formula Weight: 358.4
Purity: ?98%
Formulation: A crystalline solid
?max: 220, 300 nm
SMILES: O=C(OC1=C(C=CC=C2)C2=CC=C1)C3=NN(CCCCC)C4=CC=CC=C43
InChi CodeInChI=1S/C23H22N2O2/c1-2-3-8-16-25-20-14-7-6-13-19(20)22(24-25)23(26)27-21-15-9-11-17-10-4-5-12-18(17)21/h4-7,9-15H,2-3,8,16H2,1H3
InChi Key: JBVNFKZVDLFOAY-UHFFFAOYSA-N
Shipping & Storage Information
Storage: -20°C
Shipping: Room Temperature in continental US; may vary elsewhere
Stability: ? 2 years
WARNING This product is not for human or veterinary use.BUY SDB-005 POWDER

See also
5F-PB-22
AM-2201
BB-22
JWH-018
NM-2201
NNE1

It remains in use in scientific research applications and in amalgam for dental restoration in some locales. It is also used in fluorescent lighting. Electricity passed through mercury vapor in a fluorescent lamp produces short-wave ultraviolet light, which then causes the phosphor in the tube to fluoresce, making visible light. Mercury poisoning can result from exposure to water-soluble forms of mercury (such as mercuric chloride or methylmercury), by inhalation of mercury vapor, or by ingesting any form of mercury.

Chemical properties
Mercury does not react with most acids, such as dilute sulfuric acid, although oxidizing acids such as concentrated sulfuric acid and nitric acid or aqua regia dissolve it to give sulfate, nitrate, and chloride. Like silver, mercury reacts with atmospheric hydrogen sulfide. Mercury reacts with solid sulfur flakes, which are used in mercury spill kits to absorb mercury (spill kits also use activated carbon and powdered zinc).

Specification:
MF: C
Other Names: Activated Charcoal
Purity: 99.9%
Type: Adsorbent
Usage: Coating Auxiliary Agents,Electronics Chemicals,Leather Auxiliary Agents,Paper Chemicals,Petroleum Additives,Plastic Auxiliary Agents,Rubber Auxiliary Agents,Surfactants,Textile Auxiliary Agents,Water Treatment Chemicals
Adsorbent Variety: Activated Carbon
Physical properties
A complete explanation of mercury’s extreme volatility delves deep into the realm of quantum physics, but it can be summarized as follows: mercury has a unique electron configuration where electrons fill up all the available 1s, 2s, 2p, 3s, 3p, 3d, 4s, 4p, 4d, 4f, 5s, 5p, 5d, and 6s subshells. Because this configuration strongly resists removal of an electron, mercury behaves similarly to noble gases, which form weak bonds and hence melt at low temperatures.

The stability of the 6s shell is due to the presence of a filled 4f shell. An f shell poorly screens the nuclear charge that increases the attractive Coulomb interaction of the 6s shell and the nucleus (see lanthanide contraction). The absence of a filled inner f shell is the reason for the somewhat higher melting temperature of cadmium and zinc, although both these metals still melt easily and, in addition, have unusually low boiling points.

Occupational exposure
EPA workers clean up residential mercury spill in 2004
Due to the health effects of mercury exposure, industrial and commercial uses are regulated in many countries. The World Health Organization, OSHA, and NIOSH all treat mercury as an occupational hazard, and have established specific occupational exposure limits. Environmental releases and disposal of mercury are regulated in the U.S. primarily by the United States Environmental Protection Agency.

Applications
It is used primarily for the manufacture of industrial chemicals or for electrical and electronic applications. It is used in some thermometers, especially ones which are used to measure high temperatures. A still increasing amount is used as gaseous mercury in fluorescent lamps, while most of the other applications are slowly phased out due to health and safety regulations and is in some applications replaced with less toxic but considerably more expensive Galinstan alloy.

Production of chlorine and caustic soda
Chlorine is produced from sodium chloride (common salt, NaCl) using electrolysis to separate the metallic sodium from the chlorine gas. Usually the salt is dissolved in water to produce a brine. By-products of any such chloralkali process are hydrogen (H2) and sodium hydroxide (NaOH), which is commonly called caustic soda or lye. By far the largest use of mercury in the late 20th century was in the mercury cell process (also called the Castner-Kellner process) where metallic sodium is formed as an amalgam at a cathode made from mercury; this sodium is then reacted with water to produce sodium hydroxide. Many of the industrial mercury releases of the 20th century came from this process, although modern plants claimed to be safe in this regard. After about 1985, all new chloralkali production facilities that were built in the United States used membrane cell or diaphragm cell technologies to produce chlorine.

Treatment
Research on the treatment of mercury poisoning is limited. Currently available drugs for acute mercurial poisoning include chelators N-acetyl-D, L-penicillamine (NAP), British Anti-Lewisite (BAL), 2,3-dimercapto-1-propanesulfonic acid (DMPS), and dimercaptosuccinic acid (DMSA). In one small study including 11 construction workers exposed to elemental mercury, patients were treated with DMSA and NAP. Chelation therapy with both drugs resulted in the mobilization of a small fraction of the total estimated body mercury. DMSA was able to increase the excretion of mercury to a greater extent than NAP.

See also
Amalgam (dentistry)
Mercury poisoning
Mercury pollution in the ocean
Methylmercury
Minamata disease
Red mercury
COLEX process (isotopic separation)
Medicine
Buy mercury powder and its compounds have been used in medicine, although they are much less common today than they once were, now that the toxic effects of mercury and its compounds are more widely understood. It is an ingredient in dental amalgams. Thiomersal (called Thimerosal in the United States) is an organic compound used as a preservative in vaccines, though this use is in decline. Thiomersal is metabolized to ethyl mercury. Although it was widely speculated that this mercury-based preservative could cause or trigger autism in children, scientific studies showed no evidence supporting any such link. Nevertheless, thiomersal has been removed from, or reduced to trace amounts in all U.S. vaccines recommended for children 6 years of age and under, with the exception of inactivated influenza vaccine.

Another mercury compound, merbromin (Mercurochrome), is a topical antiseptic used for minor cuts and scrapes that is still in use in some countries.

Buy mercury powder online,  in the form of one of its common ores, cinnabar, is used in various traditional medicines, especially in traditional Chinese medicine. Review of its safety has found that cinnabar can lead to significant mercury intoxication when heated, consumed in overdose, or taken long term, and can have adverse effects at therapeutic doses, though effects from therapeutic doses are typically reversible. Although this form of mercury appears to be less toxic than other forms, its use in traditional Chinese medicine has not yet been justified, as the therapeutic basis for the use of cinnabar is not clear

Details to buy MAM-2201 crystal
Synonyms JWH 122 N-pentanoic acid metabolite
MAM2201 (Item No. 9001219) is a synthetic cannabinoid (CB) that is closely related, structurally, to AM2201 (Item No. 10707) and JWH 122 (Item No. 10591), two compounds which display high affinities for both CB receptors. MAM2201 N-pentanoic acid metabolite is a potential phase 1 metabolite of MAM2201 or JWH 122, based on the known metabolism of similar compounds. The physiological and toxicological properties of this compound have not been evaluated. This product is intended for forensic and research applications.

Technical Information
Formal Name: [1-(5-fluoropentyl)-1H-indol-3-yl](4-methyl-1-naphthalenyl)-methanone

CAS Number:1354631-24-5
Molecular Formula:
C25H24FNO
Formula Weight:
373.5
Purity:
?98%
Formulation: A neat solid
SMILES: FCCCCCN1C2=CC=CC=C2C(C(C3=CC=C(C)C4=C3C=CC=C4)=O)=C1
InChi Code: InChI=1S/C25H24FNO/c1-18-13-14-22(20-10-4-3-9-19(18)20)25(28)23-17-27(16-8-2-7-15-26)24-12-6-5-11-21(23)24/h3-6,9-14,17H,2,7-8,15-16H2,1H3
InChi Key: IGBHZHCGWLHBAE-UHFFFAOYSA-N
Shipping & Storage Information after buy MAM-2201 crystal
Storage: -20°C
Shipping: Room Temperature in continental US; may vary elsewhere
Stability: ? 2 years

Below is a list of currently available research chemicals for sale by RECENT CHEMICALS. Please contact us if you have some inquiries or simply start at the home page for your quest to order research chemicals online.

#4 Heroin
1P-LSD
2-FA
25I-NBOMe
2C-E
2C-I
2C-P
3-Methylethcathinone
4-ACO-DMT
4-FA
4-FMC Flephedrone

Why is MAM-2201 used?
MAM-2201 generally used for the following reasons: Mood enhancement, euphoria, general arousal, body pleasure, change in awareness, relaxation etc. Please note that MAM-2201 generally smoked into human body. This process can be completed chemically or with help of the herbal blends as well. Apart from being a medicine, MAM-2201 often used as a research chemical in various laboratories all over the world too.

Presumably, known to act as a potent against the cannabinoid receptors. The element initially identified in June, 2011 in German and Dutch laboratories as one of the ingredients in the synthetic cannabis smoking blends.

FUB-PB22 with the formal name of quinolin-8-yl 1-(4-fluorobenzyl)-1H-indole-3-carboxylate and is a substitute of 5F-PB22 and PB22. The molecular formula is C25H17FN2O2 with a molecular weight of 396.41 and an exact mass of 396.13. FUB-PB22 is a white powder, developed on an indazole base, which sets it apart from several other JWH compounds having an indolyl base. At this time, research on FUB-PB22 has not determined the biochemical, physiological, and toxicological properties, thus more research is needed.

Pharmacology
FUB-PB-22 acts as a full agonist with a binding affinity of 0.386nM at CB1 and 0.478nM at CB2cannabinoid receptors.

Legal status
FUB-PB-22 is a Anlage II controlled substance in Germany. It was scheduled in Japan in July 2014.

As of October 2015 FUB-PB-22 is a controlled substance in China.

It is also banned in Sweden.

Chemical and physical data
Formula: C25H17FN2O2

Molar mass: 396.41 g/mol g·mol?1

See also
5F-PB-22
AM-2201
BB-22
FUB-JWH-018
AB-FUBINACA
ADB-FUBINACA
AMB-FUBINACA
FDU-PB-22
FUB-144
FUB-APINACA
MDMB-FUBICA
MDMB-FUBINACA
PB-22

Chemical and physical data
Formula: C25H24N2O2

Molar mass: 384.47 g/mol g·mol?1

Pharmacology
Buy BB-22 Powder Online, acts as a full agonist with a binding affinity of 0.217nM at CB1 and 0.338nM at CB2 cannabinoid receptors. BB-22 is a synthetic cannabinoid and an analog of JWH 018. This certified solution is suitable as starting material for calibrators or controls in synthetic cannabinoid GC/MS or LC/MS methods for urine drug testing, forensic analysis, or clinical toxicology applications. For those synthetic cannabinoids currently controlled at the federal level, our certified solution standards of these substances are DEA-exempt, allowing laboratories to place orders without additional regulatory paperwork. For US customers, state specific regulatory requirements may apply.

BB-22 is an analog of JWH 018 that is structurally similar to PB-22 (Item No. 14096) and its derivative, 5-fluoro PB-22 (Item No. 14095). Both BB-22 and PB-22 are distinctive in that an 8-hydroxyquinoline replaces the naphthalene group of JWH 018. The physiological and toxicological properties of this compound are not known. This product is intended for forensic and research applications.

WARNING This product is not for human or veterinary use.

See also
5F-PB-22
JWH-018
PB-22
QUPIC
SDB-001
SDB-005

AM2201 (Item No. 10707) is an analytical reference material characterized as a synthetic cannabinoid.

AM2201 is regulated as a Schedule I compound in the United States.

Abstract
Novel synthetic cannabinoids are appearing in recreational drug markets worldwide. Pharmacological characterization of these new drugs is needed to inform clinicians, toxicologists, and policy makers who monitor public health. [1-(5-Fluoropentyl)-1H-indol-3-yl](1-naphthyl)methanone (AM-2201) is an abused synthetic cannabinoid that was initially created as a research tool for investigating the endocannabinoid system.

Here we measured the pharmacodynamic effects of AM-2201 in rats, and simultaneously determined plasma pharmacokinetics for the parent drug and its metabolites. Male Sprague-Dawley rats were fitted with surgically implanted temperature transponders and indwelling jugular catheters under pentobarbital anesthesia. One week later, rats received subcutaneous injection of AM-2201 (0.1, 0.3, and 1.0 mg/kg) or its vehicle, and serial blood specimens were withdrawn via catheters. Core temperatures and catalepsy were measured just prior to each blood withdrawal, and plasma was assayed for drug and metabolites using liquid chromatography-tandem mass spectrometry.

Two new types of synthetic cannabinoids, an AM-2201 benzimidazole analog (FUBIMINA, 1) and (4-methylpiperazin-1-yl)(1-pentyl-1H-indol-3-yl)methanone (MEPIRAPIM, 2), and three newly emerged phenethylamine derivatives, 25B-NBOMe (3), 2C-N-NBOMe (4), and a 25H-NBOMe 3,4,5-trimethoxybenzyl analog (5), were detected in illegal products distributed in Japan.

The identification was based on liquid chromatography–mass spectrometry (LC–MS) and gas chromatography–mass spectrometry (GC–MS), high-resolution MS, and nuclear magnetic resonance analyses. Different from the representative synthetic cannabinoids, such as JWH-018, which have a naphthoylindole moiety, compounds 1 and 2 were completely new.

Precautions
All of Croweed Products are for scientific laboratory research purposes and are not for diagnostic, therapeutics, prophylactic or in vivo use. Through your purchase, you expressly represent and warrant to Croweed that you will properly test and use any Products purchased from Croweed in accordance with industry standards. Croweed and its authorized distributors reserve the right to refuse to process any order where we reasonably believe that the intended use will fall outside of our acceptable guidelines.
Disclaimer
While every efforts were made to ensure the accuracy of the information provided in this datasheet, MyBioSource will not be liable for any omissions or errors contained herein. Croweed reserves the right to make changes to this datasheet at any time without prior notice.

It is the responsibility of the customer to report product performance issues to Croweed within 30 days of receipt of the product. Please visit our Terms & Conditions page for more information.

Technical Information
Formal Name: [1-(5-fluoropentyl)-1H-indol-3-yl]-1-naphthalenyl-methanone
CAS Number: 335161-24-5
Molecular Formula: C24H22FNO
Formula Weight: 359.4
Purity: ?98%
Formulation: A neat solid
?max: 218, 247, 315 nm
SMILES: O=C(C1=CC=CC2=C1C=CC=C2)C3=CN(CCCCCF)C4=CC=CC=C43
InChi Code: InChI=1S/C24H22FNO/c25-15-6-1-7-16-26-17-22(20-12-4-5-14-23(20)26)24(27)21-13-8-10-18-9-2-3-11-19(18)21/h2-5,8-14,17H,1,6-7,15-16H2

See also
AM-694
AM-1235
AM-2232
AM-2233
JWH-018
SDB-005
THJ-018
THJ-2201
MEPIRAPIM
NM-2201

Shipping & Storage Information
Storage: -20°C
Stability: ? 3 years

Buy AB-PINACA Crystal online at our shop, it is a compound that was first identified as a component of synthetic cannabis products in Japan in 2012.

It was originally developed by Pfizer in 2009 as an analgesic medication.

AB-PINACA acts as a potent agonist for the CB1 receptor (Ki = 2.87 nM, EC50 = 1.2 nM) and CB2 receptor (Ki = 0.88 nM, EC50 = 2.5 nM) and fully substitutes for ?9-THC in rat discrimination studies, while being 1.5x more potent.

There have been a number of reported cases of deaths and hospitalizations in relation to this synthetic cannabinoid.

AB-PINACA is a synthetic cannabinoid usually sold as a herbal smoking mixture designed to mimic THC, the active chemical of cannabis. Synthetic cannabinoids are classed as ‘New Psychoactive Substances’ (NPS) which are unregulated substances that have become newly available on the market as an alternative to illegal drugs. As a reaction to prohibition, synthetic cannabinoid producers change the compounds found in designer drugs and create new generations of synthetic drugs, such as AB-PINACA. As a result, accidental overdose and severe psychiatric complications may be more likely to occur because the type and amount of active compound may vary considerably from batch to batch. Other effects may include agitation, rapid heart rate, confusion, dizziness and nausea.

AB-PINACA
A potent CB1 and CB2 receptor agonist, AB-PINACA is a member of the aminoalkylindazole class of synthetic cannabinoids. According to the NFLIS 2014 midyear report, AB-PINACA accounted for 11% of all synthetic cannabinoid drug reports in the United States during the first half of 2014. This certified reference solution is suited for use in synthetic cannabinoid testing methods by LC/MS or GC/MS for applications in clinical toxicology, urine drug testing, and forensic analysis.

*Statement on Forensic Use Products

Forensic Use Only devices are intended for use only in drugs of abuse testing for law enforcement purposes.

Appropriate users of such devices include, for example, court systems, police departments, probation/parole offices, juvenile detention centers, prisons, jails, correction centers and other similar law enforcement entities, or laboratories or other establishments performing forensic testing for these entities.

Forensic Use Only devices are not designed, tested, developed, or labeled for use in other settings, such as clinical diagnostic or workplace settings.

Intended Use
The CEDIA® AB-PINACA assay is intended for the qualitative and semi-quantitative detection and estimation of the parent compound and metabolites of AB-PINACA, AB-CHMINACA, and AB-FUBINACA in human urine at a cutoff of 20 ng/mL. The assay is intended to be used in laboratories and provides a simple and rapid analytical screen to detect AB-PINACA-related synthetic cannabinoids compounds and metabolites in human urine. The semi-quantitative mode is for detection and for the purpose of enabling laboratories to determine an appropriate dilution of the specimen for confirmation by a confirmatory method such as Liquid chromatography/tandem mass spectrometry (LC-MS/MS) or permitting laboratories to establish quality control procedures. Clinical and professional judgment should be applied to any drug of abuse test result, particularly when preliminary positive results are used. For Criminal Justice and Forensic Use Only-Buy AB-PINACA Crystal Online.

Metabolite Analysis.
Twelve mice (n = 4 per drug) were given intraperitoneal injections of 3 mg/kg AB-PINACA, 3 mg/kg AB-CHMINACA, or 100 mg/kg FUBIMINA. Immediately following injections, the mice were placed into metabolism cages and urine was collected over a 24-hour period. Urine from mice dosed with the same compound was pooled for analysis. Samples were extracted using a salting-out liquid-liquid extraction method prior to analysis. Acetonitrile (200 µl) was added to 100 µL urine, and then the samples were vortexed and 50 µl 5 M ammonium acetate was added as a salting out agent. Samples were vortexed and centrifuged at 10,000 rcf for 5 minutes. The top aqueous layer was removed and dried down at 40°C and reconstituted with 50 µl mobile phase A.

Discussion
Psychoactive cannabinoid agonists produce a characteristic profile of in vitro and in vivo pharmacological effects, including binding to and activating CB1 receptors, dose-dependent activity in a tetrad battery of tests in mice, and ?9-THC–like discriminative stimulus effects (Wiley and Martin, 2009).

See also

5F-AB-PINACA
5F-ADB
5F-AMB
5F-APINACA
5F-CUMYL-PINACA
AB-CHFUPYCA
AB-FUBINACA
AB-PICA
ADB-CHMINACA
ADB-FUBINACA
ADB-PINACA
ADBICA
APICA
APINACA
MDMB-CHMICA
PX-3

it contains a valine amino acid amide residue as part of its structure, where older cannabinoids contained a naphthyl or adamantane residue.

Formula:
C20H28N4O2

ChemSpider ID:
30646774

IUPAC name
N-[(2S)-1-Amino-3-methyl-1-oxobutan-2-yl]-1-(cyclohexylmethyl)indazole-3-carboxamide

An Analytical Reference Standard
Item No.
28236

Purity:
?98%

Formulation:
A crystalline solid
ADB-CHMINACA (MAB-CHMINACA)
is a new synthetic cannabinoid with high potency and many reported adverse events and fatalities. The drug is currently scheduled in several countries in Europe and the USA.

Analyse
Analyse method developed to confirm ADB-CHMINACA intake for clinical and forensic programs. For many synthetic cannabinoids, parent compound is not detectable in biological samples after intake, making the detection of metabolites the only way to prove consumption. Therefore, detection of ADB-CHMINACA metabolites in biological specimens is critical.

Part Description
LP262538-4 AB-CHMINACA butanoate
AB-CHMINACA hydroxycyclohexyl and AB-CHMINACA butanoate are metabolites of AB-CHMINACA (N-[1-amino-3-methyl-oxobutan-2-yl]-1-[cyclohexylmethyl]-1H-indazole-3-carboxamide), an indazole-based synthetic cannabinoid that shows high affinity for cannabinoid CB1 and CB2 receptors.

Synthetic cannabinoids interact with the same brain receptors as THC (the active drug present in marijuana) and have been demonstrated to produce similar effects. The drug is typically sprayed on botanical material and smoked, although it can be ingested in liquid or also powder form. Products containing this drug are sold under a wide variety of names including (but not limited to) Spice, Potpourri, Smoke, K2, Zombie, Kush, and Cloud 10.

Related Names
Cfm
Cloud 10
CNFR
CNFRM
Conf
Confirmation
Confirmatory
DRUG/TOXICOLOGY
Drugs
GCMS
K2
Ordinal
Point in time
Potpourri
PR
QL
Qual
Qualitative
Random
Screen
Spice
Synthetic cannabinoid
UA
UR
Urn
Zombie

It is a 3-(tetramethylcyclopropylmethanoyl)indole derivative related to compounds such as UR-144, A-796,260 and A-834,735, but it is not specifically listed in the patent or scientific literature alongside these other similar compounds, and appears to have not previously been made by Abbott Laboratories, despite falling within the claims of patent WO 2006/069196. XLR-11 was found to produce rapid, short-lived hypothermic effects in rats at doses of 3 mg/kg and 10 mg/kg, suggesting that it is of comparable potency to APICA and STS-135.

Detection
A forensic standard for this compound is available, and a representative mass spectrum has been posted on Forendex.

Side effects
XLR-11 has been linked to hospitalizations due to its use.

Recreational use
XLR-11 was instead first identified by laboratories in 2012 as an ingredient in synthetic cannabis smoking blends, and appears to be a novel compound invented specifically for grey-market recreational use.

Chemical and physical data
Formula: C21H28FNO

Molar mass: 329.459 g·mol?1

See also
FAB-144
JWH-018
STS-135
UR-144
XLR-12

It is a 3-(tetramethylcyclopropylmethanoyl)indole derivative related to compounds such as UR-144, A-796,260 and A-834,735, but it is not specifically listed in the patent or scientific literature alongside these other similar compounds, and appears to have not previously been made by Abbott Laboratories, despite falling within the claims of patent WO 2006/069196. XLR-11 was found to produce rapid, short-lived hypothermic effects in rats at doses of 3 mg/kg and 10 mg/kg, suggesting that it is of comparable potency to APICA and STS-135.

Chemical and physical data
Formula: C21H28FNO

Molar mass: 329.459 g·mol?1

Detection
A forensic standard for this compound is available, and a representative mass spectrum has been posted on Forendex

Side effects
XLR-11 has been linked to hospitalizations due to its use

Toxicity
XLR-11 has been linked to acute kidney injury in some users, along with AM-2201.

Legal Status
XLR-11 was banned in New Zealand by being added to the temporary class drug schedule, effective from 13 July 2012.

The U.S. Drug Enforcement Administration (DEA) made the synthetic cannabinoids UR-144, XLR11, and AKB48 Schedule I, illegal drugs under the Controlled Substances Act (CSA) for the next two years as of 16 May 2013.

It has also been banned in Florida as of December 11, 2012.

Arizona banned XLR-11 on 3 April 2013.

As of October 2015 XLR-11 is a controlled substance in China.

XLR-11 is banned in the Czech Republic

See also
FAB-144
JWH-018
STS-135
UR-144
XLR-12

5-fluoro PB-22 (Item No. 14095) is an analytical reference material that is structurally categorized as a synthetic cannabinoid (CB). It is a full agonist of human CB1 and CB2 receptors (pEC50s = 8.55 and 7.97, respectively).1,2 5-fluoro PB-22 potently and dose-dependently induces hypothermia and reduces heart rate in rats, mimicking the in vivo effects of ?9-THC (Item Nos. 12068 | ISO60157).1 This product is intended for research and forensic applications.

Pharmacology
5F-PB-22 acts as a full agonist with a binding affinity of 0.468 nM at CB1 and 0.633 nM at CB2cannabinoid receptors.

Chemical and physical data
Formula: C23H21FN2O2

Molar mass: 376.431 g·mol?1

Technical Information
Formal Name1-(5-fluoropentyl)-8-quinolinyl ester-1H-indole-3-carboxylic acid
CAS Number1400742-41-7
Molecular FormulaC23H21FN2O2
Formula Weight376.4
Purity?98%
FormulationA neat solid
SMILESO=C(OC1=C(N=CC=C2)C2=CC=C1)C3=CN(CCCCCF)C4=C3C=CC=C4
InChi CodeInChI=1S/C23H21FN2O2/c24-13-4-1-5-15-26-16-19(18-10-2-3-11-20(18)26)23(27)28-21-12-6-8-17-9-7-14-25-22(17)21/h2-3,6-12,14,16H,1,4-5,13,15H2
InChi KeyMBOCMBFDYVSGLJ-UHFFFAOYSA-N
WARNING This product is not for human or veterinary use.

Shipping & Storage Information
Storage: -20°C
Shipping: Room Temperature in continental US; may vary elsewhere
Stability: ? 3 years
See also
AM-2201
JWH-018
QUCHIC
QUPIC
SDB-001
SDB-005

Synonyms MDMB-2201 5-fluoro-MDMB-2201

CAS Number 1971007-88-1
Molecular Formula C21H29FN2O3
Formula Weight 376.5
Purity ?100%
Formulation A crystalline solid ?max 217, 290 nm
Control Status 5f mdmb 2201
5F-MDMB-PICA is a Schedule I controlled substance under the Federal Controlled Substances Act.

IllicitBuy 5f-mdmb-2201 online :
The National Forensic Laboratory Information System (NFLIS), a system that collects drug analysis information from state and local forensic laboratories, contain 340 reports for 5F-MDMB-PICA between 2016 and 2018.

Storage Information
Storage: -20°C
Shipping : Room Temperature in continental US; may vary elsewhere
Stability: ? 2 years
Pharmacology:
Data from preclinical studies show that 5F-MDMBPICA binds to and acts as an agonist at the CB1 receptor. There are no published studies on the safety of 5FMDMB-PICA for human use.

MMB-2201 is the indole core analogue of 5F-AMB. Synthetic cannabinoid compounds with an indole-3-carboxamide or indazole-3-carboxamide core bearing a N-1-methoxycarbonyl group with attached isopropyl or tert-butyl substituent, have proved to be much more dangerous than older synthetic cannabinoid compounds previously reported, and have been linked to many deaths in Russia, Japan, Europe and the United States.

Pharmacology
5F-BB22 acts as a full agonist with a binding affinity of 1.94 nM at CB1 and 0.266 nM at CB2 cannabinoid receptors.

Those of you who are in the market for high-grade synthetic cannabinoid powder or Crystals for sale can easily find it at croweed. The purity of our products is without equal, not to mention how varied our range of supplements is. It includes much more than just traditional THC and CBD so that you can make your research complete.

Although they are synthetic, our cannabinoids have a close affinity with natural compounds that occur in the cannabis plant. Not only do they release their effects in the same way (by interacting with cannabinoid receptors), but they are also associated with high selectivity and little to no toxicity. Besides, our cannabinoids are proven to trigger the same nervous system responses, which is especially important for research in the area.

ADB-CHMINACA
ADB-FUBINACA
ADB-PINACA
ADBICA
APICA
APINACA
FUB-APINACA
MDMB-CHMICA
PX-3

5F-AKB48 is an Anlage II controlled drug in Germany since July 2013. As of October 2015, 5F-AKB48 is a controlled substance in China.

5F-AKB48 is banned in the Czech Republic.

5F-AKB48 was first identified in South Korea. It is expected to be a potent agonist of the CB1 receptor and CB2 receptor. Its metabolism has been described in literature.

Chemical and physical data
Formula: C23H30FN3O

Molar mass: 383.5 g/mol g·mol?1

Pharmacology
5F-AKB48 acts as a full agonist with a binding affinity of 1.94 nM at CB1 and 0.266 nM at CB2 cannabinoid receptors.

See also
5F-ADB
5F-AMB
AB-FUBINACA
AB-CHFUPYCA
AB-PINACA
ADB-CHMINACA
ADB-FUBINACA
ADB-PINACA
ADBICA
APICA
APINACA
FUB-APINACA
MDMB-CHMICA