Disulfiram
cas: 97-77-8 — see every product listed under this CAS number, including other names
Disulfiram (CAS 97-77-8) is a chemical reagent available from Chemat. Available pack sizes: on request, 250mg, 100mg, 1g, 500mg, 500g, 250g, 1000g. Offered by: Chemat Brand, Mikromol, Dr. Ehrenstorfer, GLPBio.
| brand | Chemat Brand |
|---|---|
| catalog number | ULD331 |
| cas | 97-77-8 |
| size | on request |
| availability | Do potwierdzenia przez Chemat|To be confirmed by Chemat |
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Available pack sizes
| brand | size | price | |
|---|---|---|---|
| Chemat Brand | on request | price on request | |
| Mikromol | 250mg | price on request | |
| Dr. Ehrenstorfer | 250mg | price on request | |
| GLPBio | 100mg | 517.47 Pln | |
| GLPBio | 1g | 592.36 Pln | |
| GLPBio | 500mg | 564.28 Pln | |
| Biosynth | 500g | price on request | |
| Biosynth | 250g | price on request | |
| Biosynth | 1000g | price on request | |
| Biosynth | 2000g | price on request | |
| Sigma-Aldrich | 1EA | 850.50 Pln | |
| Sigma-Aldrich | 1G | 653.60 Pln | |
| HPC Standards | 1x250mg | 268.84 Pln |
properties
| purity | No data |
|---|---|
| category | Chemicals |
| delivery time | To be confirmed by Chemat |
Disulfiram is an organic disulfide that results from the formal oxidative dimerisation of N,N-diethyldithiocarbamic acid. A multi-enzyme inhibitor that is used in alcohol aversion therapy and also exhibits anticancer properties. It has a role as a ferroptosis inducer, a fungicide, an EC 1.2.1.3 [aldehyde dehydrogenase (NAD(+))] inhibitor, an antineoplastic agent, an EC 3.1.1.8 (cholinesterase) inhibitor, an angiogenesis inhibitor, an EC 5.99.1.2 (DNA topoisomerase) inhibitor, an apoptosis inducer, a NF-kappaB inhibitor and an EC 3.1.1.1 (carboxylesterase) inhibitor. It is an organic disulfide and an organosulfur acaricide.
Source: ChEBI
| Molecular formula | C10H20N2S4 |
|---|---|
| Molecular weight | 296.5 g/mol |
| IUPAC name | diethylcarbamothioylsulfanyl N,N-diethylcarbamodithioate |
| InChIKey | AUZONCFQVSMFAP-UHFFFAOYSA-N |
| SMILES | CCN(CC)C(=S)SSC(=S)N(CC)CC |
Computed by PubChem (NCBI)