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T24201

Sigma-Aldrich

Tetramethylthiuram disulfide

97%

Sinónimos:

Bis(dimethylthiocarbamoyl) disulfide, Bis(dimethylthiocarbamyl) disulfide, Thiram

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About This Item

Fórmula lineal:
(CH3)2NCSS2CSN(CH3)2
Número de CAS:
137-26-8
Peso molecular:
240.43
Beilstein/REAXYS Number:
1725821
EC Number:
205-286-2
MDL number:
MFCD00008325
UNSPSC Code:
12352100
PubChem Substance ID:
24900038
NACRES:
NA.22

Quality Level

100

assay

97%

autoignition temp.

316 °F

mp

156-158 °C (lit.)

SMILES string

CN(C)C(=S)SSC(=S)N(C)C

InChI

1S/C6H12N2S4/c1-7(2)5(9)11-12-6(10)8(3)4/h1-4H3

InChI key

KUAZQDVKQLNFPE-UHFFFAOYSA-N

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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

Storage Class

13 - Non Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves

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Certificados de análisis (COA)

Lot/Batch Number
STBL3236
STBK4328
STBK1015
STBK0012
STBH7513

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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
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
Saadat Rastegarzadeh et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 114, 46-50 (2013-06-13)
A novel and simple method for the sensitive determination of trace amounts of fungicide thiram is developed by combination of dispersive liquid-liquid microextraction (DLLME) and microvolume UV-vis spectrophotometry. The method is based on the conversion of thiram to a yellow
O M S Filipe et al.
Chemosphere, 91(7), 993-1001 (2013-03-08)
In this study, the relevance of photodegradation processes on the persistence of the fungicide thiram in waters was investigated. The photodegradation of thiram in Milli-Q water and in aqueous solutions of humic and fulvic acids, as well as the photodegradation
Claudia S Sepúlveda et al.
Antiviral research, 87(3), 329-337 (2010-07-06)
A selected group of aromatic disulfides, thiuram disulfides and thiosulfones, provided by the National Cancer Institute, were evaluated in vitro for their inhibitory activity against Junin virus (JUNV), the causative agent of Argentine hemorrhagic fever. The aromatic disulfides NSC4492 and
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