T24201
二硫化四甲基秋兰姆
97%
别名:
二硫化双(硫羰基二甲胺), 促进剂 T, 福美双
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关于此项目
线性分子式:
(CH3)2NCSS2CSN(CH3)2
化学文摘社编号:
分子量:
240.43
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
205-286-2
Beilstein/REAXYS Number:
1725821
MDL number:
产品名称
二硫化四甲基秋兰姆, 97%
InChI key
KUAZQDVKQLNFPE-UHFFFAOYSA-N
InChI
1S/C6H12N2S4/c1-7(2)5(9)11-12-6(10)8(3)4/h1-4H3
SMILES string
CN(C)C(=S)SSC(=S)N(C)C
assay
97%
autoignition temp.
316 °F
mp
156-158 °C (lit.)
Quality Level
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signalword
Warning
Hazard Classifications
Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Irrit. 2 - Skin Irrit. 2 - Skin Sens. 1 - STOT RE 2 Oral
target_organs
Liver
存储类别
13 - Non Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
法规信息
危险化学品
农药列管产品
此项目有
Weiwei Deng et al.
PloS one, 10(6), e0129781-e0129781 (2015-06-13)
The plant circadian clock is an internal timekeeper that coordinates biological processes with daily changes in the external environment. The transcript levels of clock genes, which oscillate to control circadian outputs, were examined during early seedling development in barley (Hordeum
Agnese D'Agostino et al.
Talanta, 216, 120936-120936 (2020-05-28)
Seed-growth synthesis is a common strategy to prepare silver nanoplates, whose peculiar plasmonic features can be exploited for surface enhanced Raman scattering (SERS) applications. Here we describe the fabrication and characterization of SERS chips using a peculiar in situ seed
Toxicology of thiram (tetramethylthiuram disulfide): a review.
R R Dalvi
Veterinary and human toxicology, 30(5), 480-482 (1988-10-01)
Vaneet Kumar Sharma et al.
Journal of environmental monitoring : JEM, 5(5), 717-723 (2003-11-01)
In this review a brief introduction to thiram (tetramethylthiuram disulfide; TMTD) pesticide has been given along with other applications. All the important methods available are systematically arranged and are listed under various techniques. Some of these methods have been applied
Coco N Kapanda et al.
Journal of medicinal chemistry, 52(22), 7310-7314 (2009-11-04)
Monoglyceride lipase (MGL) inhibition may offer an approach in treating diseases in which higher 2-arachidonoyglycerol activity would be beneficial. We report here the synthesis and pharmacological evaluation of bis(dialkylaminethiocarbonyl)disulfide derivatives as irreversible MGL inhibitors. Inhibition occurs through interactions with MGL
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