InChI key
REQPQFUJGGOFQL-UHFFFAOYSA-N
InChI
1S/C6H12N2S3/c1-7(2)5(9)11-6(10)8(3)4/h1-4H3
SMILES string
CN(C)C(=S)SC(=S)N(C)C
assay
97%
mp
107-111 °C (lit.)
functional group
amine, dithiocarbamate, thioether
Quality Level
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signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Skin Sens. 1
存储类别
11 - Combustible Solids
wgk
WGK 2
flash_point_f
312.8 °F - closed cup
flash_point_c
156 °C - closed cup
ppe
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
Q Li et al.
Toxicology, 104(1-3), 17-23 (1995-12-15)
To examine the validity of a modified lymphocyte transformation test for evaluating contact hypersensitivity from weak sensitizers, guinea pigs were sensitized with formaldehyde (F) or tetramethylthiuram monosulfide (TMTM) using the maximization test procedure. Lymph node cells from the animals were
B B Knudsen et al.
Contact dermatitis, 34(6), 410-413 (1996-06-01)
An estimate of amounts of thiurams that may be released from rubber gloves into synthetic sweat, has previously been generated. These amounts should be compared to elicitation thresholds of patch tests performed with serial dilutions of thiuram mix using synthetic
Contact allergy to Nobecutan.
B Pock-Steen
Contact dermatitis, 18(1), 52-53 (1988-01-01)
E Schreiner et al.
Toxicology letters, 25(2), 147-152 (1985-05-01)
The epoxide hydrolase (EH) activity in the liver of adult female Wistar rats significantly increased 18 h after the administration by gavage of tetramethyl thiuramdisulfide (TMTD, 1 mmol/kg) or tetramethyl thiurammonosulfide (TMTM, 2 mmol/kg). No increase was observed 5 h
Delayed ethanol elimination from rat blood after treatment with thiram, tetramethylthiuram monosulfide, ziram, or cyanamide.
K G Römer et al.
Bulletin of environmental contamination and toxicology, 32(5), 537-542 (1984-05-01)
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