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Chemical Identity & Background

Pyrazolam is a pyrazolo-benzodiazepine, a synthetic psychoactive compound structurally related to traditional benzodiazepines but containing a pyrazolo ring fused to the core benzodiazepine scaffold.
Its full chemical name is 8-bromo-1-methyl-6-(2-chlorophenyl)-4H-[1,2,4]-triazolo[4,3-a][1,4]-benzodiazepine.
This structure makes it closely related to alprazolam and triazolam, but it was developed primarily for research purposes and was never licensed for medical use in any country.

In its raw form, Pyrazolam typically appears as a white to off-white crystalline powder. It has been distributed in “research chemical” markets, sometimes pressed into tablets or dissolved in liquid for measurement purposes.

Pharmacology and Mechanism of Action

Pyrazolam acts as a positive allosteric modulator of GABA_A receptors, enhancing the action of the inhibitory neurotransmitter GABA. This produces the classic benzodiazepine-type effects:

• Anxiolytic (anti-anxiety)

• Sedative/hypnotic

• Anticonvulsant

• Muscle relaxant

However, pharmacological studies and anecdotal toxicology data show that Pyrazolam is distinct in that it lacks significant hypnotic or muscle-relaxant action at typical active doses. Instead, it produces primarily anxiolytic and calming effects without strong sedation.

This difference has made it a subject of pharmacological interest, since it may interact with certain GABA_A receptor subtypes differently than other benzodiazepines.

Potency and Pharmacokinetics

Pyrazolam is considered a moderate-potency benzodiazepine analogue, with activity comparable to or slightly higher than alprazolam on a milligram-to-milligram basis.

Pharmacokinetic data indicate:

• Rapid onset: within 30–60 minutes of exposure.

• Elimination half-life: roughly 17–22 hours, allowing for once-daily pharmacological activity.

• No active metabolites, meaning the compound itself is responsible for its duration of effect, unlike diazepam or diclazepam, which have long-lasting breakdown products.

Because of the absence of active metabolites, pyrazolam’s sedative effects tend to be shorter-lived and more predictable, though this also increases withdrawal potential with frequent exposure.

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Diclazepam, also known as 2’-chloro-diazepam or chlorodiazepam, is a benzodiazepine analogue in the 1,4-benzodiazepine class. Chemically, it is closely related to diazepam and was first synthesized in the 1960s, but it has never been approved for medical use. In its raw form, diclazepam appears as a white or off-white crystalline powder, often distributed as a “research chemical” or found in illicit markets. It is commonly studied in forensic laboratories to understand the emergence of designer benzodiazepines.

Pharmacology and Mechanism of Action

Diclazepam acts as a positive allosteric modulator at GABA_A receptors, enhancing the inhibitory effects of GABA in the central nervous system. This produces sedative-hypnotic, anxiolytic, anticonvulsant, and muscle-relaxant effects, similar to clinically used benzodiazepines.

Pharmacokinetic studies in animal models and human analogues suggest that diclazepam has a long duration of action with an estimated half-life of 42–60 hours for its parent compound, though active metabolites (including lorazepam, desmethyldiazepam, and delorazepam) contribute to prolonged pharmacological effects. The potency of diclazepam is slightly higher than diazepam in some reports, meaning small doses can produce noticeable sedative effects.

Powder Form 

The “powder” refers to the unformulated active pharmaceutical ingredient (API). In legitimate pharmaceutical contexts, APIs are carefully measured and formulated into tablets or capsules. In illicit or “research chemical” markets, diclazepam powder may be sold directly or encapsulated, sometimes mislabeled as diazepam or other benzodiazepines.

Medical Use and Dosing

Diclazepam has never been approved as a therapeutic drug, so there is no standardized medical dosing. Its pharmacological effects are inferred from diazepam analogues and limited human case reports. In the context of research and forensic toxicology, doses are typically reported in milligram ranges for observed sedative effects, but potency varies depending on purity and formulation. Because it is unapproved and unregulated in most countries, human use carries significant risks.

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Flubromazolam is a triazolobenzodiazepine (TBZD), a structural class closely related to other benzodiazepines but with a fused triazole ring. Its chemical name is 8-bromo-6-(2-fluorophenyl)-1-methyl-4H-[1,2,4]triazolo[4,3-a][1,4]benzodiazepine, and it has been catalogued in chemical reference databases such as PubChem. It appears as a white crystalline powder when sold in raw active form. Flubromazolam was first described in the 1970s in pharmaceutical research, but unlike therapeutic benzodiazepines such as diazepam or alprazolam, it was never approved for medical use. Instead, it has emerged in recent decades as a designer benzodiazepine, sold online as a so-called “research chemical.”

Pharmacology and potency

Flubromazolam is a positive allosteric modulator at the GABA_A receptor. Like other benzodiazepine-type compounds, it enhances the effect of the inhibitory neurotransmitter GABA, producing sedative, anxiolytic, hypnotic, muscle relaxant, and anticonvulsant effects.

One of the most notable features of flubromazolam is its extraordinary potency. Case reports and pharmacological studies indicate that doses as low as 0.25–0.5 mg may cause intense sedation, amnesia, and impaired motor coordination. At higher exposures, profound unconsciousness and respiratory depression have been observed, especially when combined with other central nervous system depressants (opioids, alcohol, gabapentinoids).

Its elimination half-life has been reported in the range of 18–36 hours, meaning that sedation can persist well into the next day, contributing to accidental overdosing when redosing occurs before the prior dose has cleared.

Powder form — significance and risks

In regulated pharmaceutical contexts, active pharmaceutical ingredients (APIs) like benzodiazepines are formulated into tablets or capsules with precise dosing controls. Flubromazolam, however, is typically distributed in illicit settings as unformulated powder or dissolved into blotters/liquids for easier handling.

Because active doses are measured in micrograms, powder form carries extreme risk: even tiny measurement errors can multiply the effective dose several times. Contamination, uneven distribution in homemade formulations, and mislabeling as more common benzodiazepines (e.g., alprazolam or diazepam) further heighten the danger.

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Clonazolam (also written clonitrazolam in some sources) is a triazolobenzodiazepine (TBZD) a benzodiazepine-type structure in which a triazole ring is fused to the core benzodiazepine scaffold. It is chemically related to clonazepam (hence the name) and typically appears as a white to off-white crystalline powder when supplied as the active substance. Chemical databases list its molecular formula and identifiers (e.g., PubChem CID 12317881).

Pharmacology and effects (high level)
Pharmacologically, clonazolam acts as a positive allosteric modulator at GABA_A receptors — the same receptor family targeted by clinically used benzodiazepines. This produces sedative-hypnotic, anxiolytic, muscle-relaxant, and amnesic effects typical of benzodiazepines. Published reviews and toxicology reports note that clonazolam is highly potent compared with many classical benzodiazepines: sedative and amnestic effects have been reported at very small oral doses (for example, a 0.5 mg dose is described in case reports as producing strong sedation and amnesia). Because potency is high, dose-related risks are substantial.

Why the powder form matters
The “powder” is simply the raw active pharmaceutical ingredient (API) unformulated into tablets or capsules. In legitimate pharmaceutical production the API is handled under strict quality control and formulated to ensure accurate dosing. In illicit or designer-drug contexts, clonazolam powder may be sold directly, weighed into capsules, or pressed into counterfeit tablets. Powders are particularly hazardous because small measurement errors can produce large differences in dose — a critical issue for high-potency TBZDs. Accidental exposure, contamination of equipment, and mislabelled products are common concerns in forensic casework and public-health reports.

Clinical use and approval status
Clonazolam is not an approved medication in most countries and lacks a recognized medical prescribing history comparable to licensed benzodiazepines such as clonazepam. It was synthesized decades ago but was never developed as an approved therapeutic agent; instead it has emerged primarily as a designer benzodiazepine in illicit markets and in “research chemical” catalogues. Scientific reviews and regulatory evaluations treat it as a non-medical substance with significant abuse potential.

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Buy Akorn Cough Syrup: Akorn, Inc., a leading area of expertise pharmaceutical business enterprise, has launched promethazine hydrochloride and phenylephrine hydrochloride syrup (promethazine/phenylephrine) and codeine phosphate syrup CV (promethazine/phenylephrine/codeine). The launches follow the approval of abbreviated new drug programs (andas) for both products from the usa meals and Drug management (FDA) in December 2014.

The 2 merchandise complement Akorn’s existing promethazine formulations which include promethazine hcl oral solution, USP; promethazine hcl and codeine phosphate syrup CV; and promethazine hcl and dextromethorphan hcl oral solution.

Akorn’s promethazine/phenylephrine syrup is indicated for the brief remedy of upper respiratory signs and symptoms, such as nasal congestion, related to hypersensitivity or the common bloodless. Marketed underneath Akorn’s hello-tech Pharmacal label, fruit-flavored promethazine/phenylephrine syrup is available in a 473 ml bottle.

About Promethazine/Phenylephrine Syrup

Akorn’s Promethazine/Phenylephrine Syrup is indicated for the transient relief of upper respiration symptoms, consisting of nasal congestion, related to allergic reaction or the common bloodless. Marketed under Akorn’s Hello-tech Pharmacal label, fruit-flavored Promethazine/Phenylephrine Syrup is available in a 473 ml bottle.

According to IMS Health, branded and accepted income of Promethazine/Phenylephrine Syrup were about $nine million for the three hundred and sixty-five days ended July 31, 2015.

About Promethazine/Phenylephrine/Codeine Syrup

Akorn’s Promethazine/Phenylephrine/Codeine Syrup is indicated for the transient comfort of coughs and top respiratory signs and symptoms, such as nasal congestion, associated with allergy and the not unusual bloodless. Also advertised beneath Akorn’s hi-Tech Pharmacal label, fruit-flavored Promethazine/Phenylephrine/Codeine Syrup is available in 118 ml and 473 ml bottles.

Approximately Akorn

Akorn, Inc. Is a forte pharmaceutical company engaged in the development, manufacture, and advertising of multisource and branded pharmaceuticals? Akorn has production facilities located in Decatur, Illinois; Somerset, New Jersey; Amityville, NY; Hettlingen, Switzerland and Paonta Sahib, India in which the employer manufactures ophthalmic, injectable, and strong point sterile and non-sterile pharmaceuticals.

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What’s ‘purple Drank’ aka Lean

That is a time period used for a recreational drink that mixes the subsequent:

Liquid medicines that can be bought over the counter from a pharmacy (or through prescription and online) that incorporate codeine, promethazine or dextromethorphan.  These can be bought as character medicines and combined together.

Smooth drinks

Fruit-flavored candies to enhance taste

Whilst these drug treatments are blended collectively to create ‘pink drank’ customers can easily lose song of the way much of the active drug they have got ate up because the liquid is masked via satisfactory or familiar flavors from soft drinks.

What are the effects of taking ‘crimson drank’?

Those will vary depending on the contents of the drink. But, customers have stated euphoric and dissociative effects.

Different outcomes might also include:

Constricted scholars

Gradual or slurred speech

Out-of-control eye motion

Droopy eyes

Slowed heart price

Drowsiness, lack of balance

Loss of coordination

Paleness

The potential to drive may be additionally be impaired, and younger humans have complained of ‘memory issues’ after taking the drink.

There’s a chance of overdose especially due to using codeine, which can be improved when taken in aggregate with alcohol.

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Descriptions – Promethazine Codeine Cough Syrup

Promethazine Codeine Cough Syrup: Promethazine and codeine aggregate are used to relieve cough, runny or stuffy nose, sneezing, or different symptoms due to allergic reactions or the common bloodless.

Promethazine is an antihistamine. It really works by means of preventing the results of a substance referred to as histamine, that is produced by the frame. Histamine can cause itching, sneezing, runny nose, and watery eyes. It is able to from time to time close up the bronchial tubes (air passages of the lungs) and make respiratory difficult. Codeine belongs to the group of drugs known as narcotic analgesics (pain medicines). It acts on the critical anxious gadget (CNS) to relieve pain.

Promethazine-codeine cough syrup is a medication that consists of codeine, an opioid that acts as a cough suppressant and can also produce relaxation and euphoria whilst consumed at a higher-than-prescribed dose. It also carries promethazine hcl, an antihistamine that moreover acts as a sedative. Even though best available through prescription, promethazine-codeine cough syrup is on occasion diverted for abuse.

How Promethazine/codeine works

Promethazine/codeine is a combination of two medicinal drugs: promethazine and codeine. Promethazine is a phenothiazine medication that blocks the indicators on your brain and frame inflicting you to enjoy cold and hypersensitivity signs like a runny nose and sneezing. Codeine is an opioid medication that works to your mind to reduce your urge to cough.Buy Promethazine Lean Alberta , Buy cough syrup Online Canada , Where to order Codeine Syrup Grande Prairie , purple drank for sale St. Albert

What is Promethazine/codeine used for?

Respiratory signs as a result of allergic reactions or the commonplace cold, such as cough, runny nose, and sneezing

How must I exploit this medicine?

Take this remedy by means of mouth. Comply with the directions on the prescription label. You can take it without or with food. If it upsets your stomach, take it with meals. Use a mainly marked spoon or container to measure each dose. Ask your pharmacist in case you do now not have one. Family spoons aren’t correct. Do not to overfill. Rinse the measuring device with water after every use. Take your medicine at ordinary periods. Do not take it more regularly than directed.

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Buy Codeine: Codeine is an opioid ache reliever used to treat mild to moderately severe aches. It is also used, commonly in a mixture with other medicinal drugs, to lessen coughing. Codeine is available as an unmarried-factor product, or in aggregate with acetaminophen or aspirin, and in a few cough and bloodless medications.

What is codeine?

Codeine is an opioid pain reliever that’s used to treat moderate to reasonably intense pain and to assist lessen coughing. Codeine is available as a single-aspect tablet and additionally available in multi-component products blended with different pain-relieving drug treatments or bloodless and flu drugs.

Dosing consideration

Get entry to naloxone for opioid overdose

Examine the need for naloxone upon beginning and renewing the remedy

Keep in mind prescribing naloxone

Based on the patient’s threat elements for overdose (eg, concomitant use of CNS depressants, a record of opioid use ailment, prior opioid overdose); the presence of chance elements should not save you right ache management

Household contributors (along with children) or other near contacts at risk for unintended ingestion or overdose

Seek advice from patients and caregivers on the subsequent:

Availability of naloxone for emergency treatment of opioid overdose

Approaches to attain naloxone as permitted by means of person kingdom doling out and prescribing necessities or guidelines (eg, by means of prescription, without delay from a pharmacist, as part of a network-based total program)

How do humans take it?

Codeine is used to treat mild to slight pain and diarrhea. People typically swallow it in drugs.

On its personal, codeine is a prescription-only opiate painkiller. It’s used to treat pain that can’t be stopped by way of extra commonplace painkillers. This means you couldn’t buy it legally without a prescription.

Small quantities of codeine are on occasion combined with different medicines – like paracetamol, ibuprofen, and aspirin – and those may be offered by a chemist or pharmacy.

Because codeine is noticeably addictive, medicines that contain it (which include co-codamol) deliver warnings on the packs about the threat of addiction. They advise that the character taking the medicine doesn’t take it for extra than three days at a time without scientific advice.

Those who take codeine illegally, or abuse their prescription (don’t take it how they need to), on occasion, overwhelm up the pills and snicker them.

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Codeine Linctus Oral Solution: Take this medicine handiest as directed by using your physician. Do no longer take extra of it, do not take it more often, and do not take it for an extended time than your doctor ordered. If an excessive amount of of this medicinal drug is taken for a long time, it may end up dependency-forming and purpose mental or physical dependence.

This medicinal drug has to include a medicine manual. Study and comply with those commands cautiously. Ask your physician if you have any questions.

Measure the oral liquid with a marked measuring spoon, oral syringe, or medicine cup. The common family teaspoon might not maintain the proper amount of liquid.

Dosing Guide

The dose of this medicinal drug can be exclusive for unique sufferers. Comply with your doctor’s orders or the instructions at the label. The following data includes handiest the average doses of this medicinal drug. If your dose is exclusive, do not change it until your health practitioner tells you to do so.

The number of drugs which you take depends on the electricity of the medicine. Additionally, the number of doses you are taking every day, the time allowed among doses, and the duration of time you are taking the medication depend on the scientific hassle that you are the use of the medication.

For remedy of symptoms due to allergic reactions or the not unusual bloodless:

For oral dosage shape (answer):

Adults and children 12 years of age and older—5 milliliters (ml) (1 teaspoonful) each four to 6 hours. Do not take greater than 30 ml in 24 hours.

Children more youthful than 12 years of age—Use isn’t always recommended.

For oral dosage form (syrup):

Adults and youngsters 12 years of age and older—5 milliliters (ml) (1 teaspoonful) each four to 6 hours. Do not take more than 30 ml in 24 hours.

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Youngsters more youthful than 6 years of age—Use isn’t encouraged.

How and while to take codeine

Observe your medical doctor’s instructions approximately the way to take this remedy. This is specifically essential due to the fact codeine can be addictive.

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Codeine actually acts directly at the nervous system and suppresses pain signals. Codeine basically silences the pain and does not diminish the reason behind the pain, hence it is recommended that you must take medical advice from a healthcare specialist after using it if you are buying it online. It has been declared a prescription drug because its prolonged use causes drug addiction. Buy Codeine Online Without Prescription.

The benefits of Codeine are:

Codeine has proved to be an important drug among all analgesics because of its long-term pain-relieving feature.

–Used to treat minor to moderate degrees of pain
-Used as cough medicine
-Used to treat diarrhea
Greater benefits are taken with the combination of other drugs

Side Effects of Codeine

Likewise, in other medicines, Codeine also has side effects. The severity of these side effects depends upon the usage of the drug. It is therefore highly recommended that you use this drug with a prescription to avoid mighty side effects. However, not all the side effects are experienced by the patients but some of the most common and major side effects are:

-Nausea
-Vomiting
-Dizziness
-Constipation
-Itchiness

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it is used to treat anxiety and panic disorders. It belongs to a class of medications called benzodiazepines which act on the brain and nerves (central nervous system) to produce a calming effect. It works by enhancing the effects of a certain natural chemical in the body (GABA).

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Buy Etizolam Powder Etizolam (marketed under many brand names) is a thienodiazepine derivative which is a benzodiazepine analog. The etizolam molecule differs from a benzodiazepine in that the benzene ring has been replaced by a thiophene ring and triazole ring has been fused, making the drug a thienotriazolodiazepine. It possesses amnesic, anxiolytic, anticonvulsant, hypnotic, sedative and skeletal muscle relaxant properties.

It was patented in 1972 and approved for medical use in 1983.

Pharmacology
Etizolam pills
Etizolam, a thienodiazepine derivative, is absorbed fairly rapidly, with peak plasma levels achieved between 30 minutes and 2 hours. It has a mean elimination half life of about 3.5 hours. Etizolam possesses potent hypnotic properties, and is comparable with other short-acting benzodiazepines. Etizolam acts as a full agonist at the benzodiazepine receptor to produce its range of therapeutic and adverse effects.Buy Etizolam Powder Online Alberta  , Buy research chemical Edmonton , Etizolam Powder for sale in Calgary , Purchase Depressants Lethbridge

According to the Italian P.I. sheet, etizolam belongs to a new class of diazepines, thienotriazolodiazepines. This new class is easily oxidized, rapidly metabolized, and has a lower risk of accumulation, even after prolonged treatment. Etizolam has an anxiolytic action about 6 times greater than that of diazepam. Etizolam produces, especially at higher dosages, a reduction in time taken to fall asleep, an increase in total sleep time, and a reduction in the number of awakenings. During tests, there were no substantial changes in deep sleep; however, it may reduce REM sleep. In EEG tests of healthy volunteers, etizolam showed some similar characteristics to tricyclic antidepressants.

Interactions
Itraconazole and fluvoxamine slow down the rate of elimination of etizolam, leading to accumulation of etizolam, therefore increasing its pharmacological effects.Carbamazepine speeds up the metabolism of etizolam, resulting in reduced pharmacological effects.

Overdose
Cases of intentional suicide by overdose using etizolam in combination with GABA agonists have been reported. Although etizolam has a lower LD50 than certain benzodiazepines, the LD50 is still far beyond the prescribed or recommended dose. Flumazenil, a GABA antagonist agent used to reverse benzodiazepine overdoses, inhibits the effect of etizolam as well as classical benzodiazepines such as diazepam and chlordiazepoxide.

Etizolam overdose deaths are rising – for instance, the National Records of Scotland report on drug-related deaths, implicated 548 deaths from ‘street’ Etizolam in 2018, almost double the number from 2017 (299) and only six years from the first recorded death (in 2012). The 548 deaths were 45% of all drug-related deaths in Scotland in 2018.

Misuse
Etizolam is a drug of potential misuse. Cases of etizolam dependence have been documented in the medical literature. However, conflicting reports from the World Health Organization, made public in 1991, dispute the misuse claims. Since 1991, cases of etizolam misuse and addiction have substantially increased, due to varying levels of accessibility and cultural popularity.

Chemical and physical data
Formula: C17H15ClN4S

Molar mass: 342.07 g/mol g·mol?1

See also
Alprazolam
Brotizolam
Clotiazepam
Deschloroetizolam
Metizolam
Benzodiazepine dependence
Benzodiazepine withdrawal syndrome
Long-term effects of benzodiazepines
Medical uses

Short-term treatment of insomnia
Short-term treatment of anxiety or panic attacks, if a benzodiazepine is required

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Trefentanil has terribly similar effects to alfentanil, very like those of fentanyl itself but more potent and shorter lasting. aspect effects of Sublimaze analogs are almost like those of fentanyl itself, that embody itching, nausea and doubtless serious metastasis depression, which may be life-threatening. Fentanyl analogs have killed many folks throughout Europe and therefore the former Soviet republics since the foremost recent improvement in use began in Baltic State within the early 2000s, and novel derivatives still appear. the chance of respiratory depression is very high with potent fentanyl analogues cherish alfentanil and trefentanil, and these medication cause a big risk of death if used outside of a hospital setting with applicable artificial respiratory apparatus available.

Clinical information
ATC code: none

Chemical and physical data
Formula: C25H31FN6O2

obtain Trefentanyl Powder online, it’s most almost like short-acting fentanyl analogues cherish alfentanil. In comparative studies, trefentanil was slightly less assailable and shorter acting than alfentanil as an analgesic, however elicited considerably additional severe metastasis depression. For this reason trefentanil has not been adopted for clinical use, though it is still utilized in research.

Trefentanil has terribly similar effects to alfentanil, very like those of fentanyl itself but more potent and shorter lasting. aspect effects of Sublimaze analogs are almost like those of fentanyl itself, that embody itching, nausea and doubtless serious metastasis depression, which may be life-threatening. Fentanyl analogs have killed many folks throughout Europe and therefore the former Soviet republics since the foremost recent improvement in use began in Baltic State within the early 2000s, and novel derivatives still appear. the chance of respiratory depression is very high with potent fentanyl analogues cherish alfentanil and trefentanil, and these medication cause a big risk of death if used outside of a hospital setting with applicable artificial respiratory apparatus available.

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Buy 4-Phenylfentanyl Powder (4-Phenylfentanyl) is an opioid analgesic that is a derivative of fentanyl. It was developed during the course of research that ultimately resulted in super-potent opioid derivatives such as carfentanil, though it is a substantially less potent analogue. 4-Phenylfentanyl is around eight times the potency of fentanyl in analgesic tests on animals, but more complex 4-heteroaryl derivatives such as substituted thiophenes and thiazoles are more potent still, as they are closer bioisosteres to the 4-carbomethoxy group of carfentanil.

Side effects of fentanyl analogs are similar to those of fentanyl itself, which include itching, nausea and potentially serious respiratory depression, which can be life-threatening. Fentanyl analogs have killed hundreds of people throughout Europe and the former Soviet republics since the most recent resurgence in use began in Estonia in the early 2000s, and novel derivatives continue to appear.

Potency and pharmacology (mechanism of action)
Like fentanyl, 4-Phenylfentanyl is a mu-opioid receptor agonist. That means it binds to the same receptor systems as morphine, heroin and fentanyl to produce analgesia, sedation and euphoria — but also the serious side effects associated with opioid receptor activation. Published pharmacology summaries and animal data indicate that some 4-substituted fentanyl analogues can be substantially more potent than morphine and, in some comparative tests, several times as potent as fentanyl itself. The potency varies by analogue and by experimental assay, but fentanyl-type compounds are well known for high potency at very low doses.

Chemical Profile

• Class: Synthetic opioid, fentanyl analogue

• Chemical name: N-Phenyl-N-[1-(2-phenylethyl)piperidin-4-yl]propanamide

• Form: Often found as a fine white or off-white powder

• Potency: Significantly more potent than morphine, but potency can vary depending on the analogue

Canonical SMILES
CCC(=O)N(C1=CC=CC=C1)C2(CCN(CC2)CCC3=CC=CC=C3)C4=CC=CC=C4

Registry Number
Linked Records

Compounds: 313,587
Substances: 390,235
Classification (Parent Nodes)

ChemIDplus Chemical Information Classification
Shipping & Storage Information
Storage: -20°C
Shipping: Room Temperature in continental US; may vary elsewhere
Stability: ? 2 years