| Identification | Back Directory | [Name]
sulfiram | [CAS]
95-05-6 | [Synonyms]
Kutka
Tetmos
Sanigal
Kutkasin
sulfiram
Tetrucid
NSC 36731
SulfiraMuM
Sarcocide B
CTPKSRZFJSJGML-UHFFFAOYSA-N
Tetraethylthiuram monosulfide
TETRAETHYLTHIURAMMONOSULPHIDE
Bis(diethylthiocarbaMyl)sulfide
BIS(DIETHYLTHIOCARBAMOYL)SULPHIDE
Bis(N,N-diethylthiocarbaMoyl)sulfide
Bis[(diethylaMino)thioxoMethyl]sulfide
1,1'-Thiobis[N,N-diethylMethanethioaMide
N,N,N',N'-Tetraethylthiodicarbonic DiaMide
DiethylcarbaModithioic Acid Anhydrosulfide
diethylcarbamothioyl N,N-diethylcarbamodithioate
Thiodicarbonic diamide ((H2N)C(S)2S), tetraethyl-
N,N-diethylcarbamodithioic acid diethylthiocarbamoyl ester | [EINECS(EC#)]
202-387-3 | [Molecular Formula]
C10H20N2S3 | [MDL Number]
MFCD00129782 | [MOL File]
95-05-6.mol | [Molecular Weight]
264.474 |
| Chemical Properties | Back Directory | [Melting point ]
30-32° | [density ]
1.1200 | [refractive index ]
1.5500 (rough estimate) | [storage temp. ]
2-8°C | [solubility ]
Chloroform (Slightly), Methanol (Slightly) | [form ]
Low-Melting Solid | [color ]
Light Yellow to Yellow | [Stability:]
Light Sensitive | [Major Application]
pharmaceutical
pharmaceutical small molecule | [InChI]
InChI=1S/C10H20N2S3/c1-5-11(6-2)9(13)15-10(14)12(7-3)8-4/h5-8H2,1-4H3 | [Contact allergens]
This rubber vulcanization accelerator is also used as an ectoparasiticide against Sarcoptes scabiei, louses, or in veterinary medicine. | [InChIKey]
CTPKSRZFJSJGML-UHFFFAOYSA-N | [SMILES]
N(CC)(CC)C(=S)SC(=S)N(CC)CC | [CAS DataBase Reference]
95-05-6 | [EPA Substance Registry System]
Thiodicarbonic diamide ([(H2N)C(S)]2S), tetraethyl- (95-05-6) |
| Hazard Information | Back Directory | [Chemical Properties]
Yellow Low Melting Solid | [Uses]
Ectoparasiticide. Used in combination pesticide compositions for controlling infestation. | [Uses]
As vulcanization agent. | [Definition]
ChEBI: Sulfiram is an organosulfur compound. | [Production Methods]
Commercial production of sulfiram relies on a straightforward thiuram disulphide synthesis: manufacturers react dimethylamine with carbon disulfide under alkaline conditions to form sodium dimethyldithiocarbamate, then oxidise this intermediate, typically with air, hydrogen peroxide, or another mild oxidant, to couple two dithiocarbamate units into the disulphide. The resulting sulfiram is isolated as a solid, washed to remove inorganic salts, and dried before being milled to the desired particle size for formulation. | [Mechanism of action]
Dithiocarbamate compounds typically work by disrupting enzyme activity, leading to neurological dysfunction and death in target pests | [Pesticide Type]
Acaricide. Insecticide |
| Safety Data | Back Directory | [RIDADR ]
2811 | [WGK Germany ]
WGK 3 | [HazardClass ]
6.1(b) | [PackingGroup ]
III | [Storage Class]
11 - Combustible Solids | [Hazard Classifications]
Acute Tox. 4 Oral
Aquatic Acute 1
Aquatic Chronic 1
STOT RE 2 |
|
|