DISULFIRAM

Disulfiram inhibits aldehyde dehydrogenase, producing aversive reactions to alcohol. Used in alcohol dependence. Side effects include flushing, nausea, neuropathy, and liver toxicity. Only GMP materials will be supplied, logistics all according to GDP.

Product Description


Mechanism of Action

Disulfiram is an aldehyde dehydrogenase (ALDH) inhibitor that blocks the oxidation of acetaldehyde to acetic acid. In the presence of ethanol, acetaldehyde accumulates, producing flushing, tachycardia, nausea and hypotensionan aversive reaction that discourages alcohol consumption. It also inhibits dopamine hydroxylase and interacts with metaldependent enzymes.

Benefits and Advantages

Used in alcoholdeterrent mechanism studies, ALDHenzyme research, addictionpathway modelling, and metalchelation/thiuram disulfide interaction assays.

Side Effects and Risks

Risks include hepatotoxicity, neuropathy, psychosis, severe disulfiramethanol reaction, dermatologic reactions and drugdrug interactions. Handle with enzymeinhibitor and hepatotoxiccompound precautions.

Only GMP materials will be supplied, logistics all according to GDP.

Datasheet


Molecular Formula

C10H20N2S4

Molecular Weight

296.5 g/mol

CAS Number

97-77-8

Storage Condition

Commercially available disulfiram tablets should be protected from light and stored in tight, light-resistant containers at a temperature less than 40 °C preferably between 15-30 °C. Oral suspensions of disulfiram have been prepared extemporaneously from commercially available tablets of the drug. A suspension of 1% disulfiram, 1/4% methylcellulose, and 10% Tang /breakfast drink/ in distilled water has been reported to be stable for up to 6 months if refrigerated at 2-8 °C and protected from light.

Solubility

less than 0.1 mg/mL at 70 °F (NTP, 1992)

Purity

Purity information is available upon request (COA).

Synonym

disulfiram; Tetraethylthiuram disulfide; 97-77-8; Antabuse; Bis(diethylthiocarbamoyl) disulfide

IUPAC/Chemical Name

diethylcarbamothioylsulfanyl N,N-diethylcarbamodithioate

InChl Key

AUZONCFQVSMFAP-UHFFFAOYSA-N

InChl Code

InChI=1S/C10H20N2S4/c1-5-11(6-2)9(13)15-16-10(14)12(7-3)8-4/h5-8H2,1-4H3

References

https://pubchem.ncbi.nlm.nih.gov/compound/3117;

3D Conformer.

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