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T24201

Sigma-Aldrich

Tetramethylthiuram disulfide

97%

Synonym(s):

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

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10000 UNITS
CA$344.00

About This Item

Linear Formula:
(CH3)2NCSS2CSN(CH3)2
CAS Number:
137-26-8
Molecular Weight:
240.43
Beilstein:
1725821
EC Number:
205-286-2
MDL number:
MFCD00008325
UNSPSC Code:
12352100
PubChem Substance ID:
24900038
NACRES:
NA.22

CA$344.00

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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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1 of 4

This Item
86720B21805549312
Tetramethylthiuram disulfide 97%

T24201

Tetramethylthiuram disulfide

Tetraethylthiuram disulfide ≥97.0% (S)

86720

Tetraethylthiuram disulfide

Dibenzyl disulfide 98%

B21805

Dibenzyl disulfide

3,3′-Dihydroxydiphenyl disulfide 97%

549312

3,3′-Dihydroxydiphenyl disulfide

assay

97%

assay

≥97.0% (S)

assay

98%

assay

97%

Quality Level

100

Quality Level

200

Quality Level

100

Quality Level

100

mp

156-158 °C (lit.)

mp

69-71 °C (lit.)

mp

69-72 °C (lit.)

mp

89-93 °C (lit.)

autoignition temp.

316 °F

autoignition temp.

-

autoignition temp.

-

autoignition temp.

-

Signal Word

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 Code

13 - Non Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
STBK4328
STBK1015
STBK0012
STBH7513
STBF1299V

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J P Doucet et al.
The Journal of biological chemistry, 266(26), 17613-17620 (1991-09-15)
The presence of low molecular weight GTP-binding proteins was investigated in subcellular fractions from skeletal muscle. Skeletal muscle homogenate, transverse tubules, triads, sarcoplasmic reticulum membranes, and cytosol fractions were separated in sodium dodecyl sulfate-gel electrophoresis and blotted onto nitrocellulose. The
I Pérez-Dorado et al.
Molecular oral microbiology, 27(4), 221-245 (2012-07-05)
Surface-exposed proteins of pathogenic bacteria are considered as potential virulence factors through their direct contribution to host-pathogen interactions. Four families of surface proteins decorate the cell surface of the human pathogen Streptococcus pneumoniae. Besides lipoproteins and LPXTG proteins, also present
Katarzyna A Broniowska et al.
American journal of physiology. Heart and circulatory physiology, 299(4), H1212-H1219 (2010-08-03)
S-nitrosothiols are nitric oxide (NO)-derived molecules found in biological systems. They have been variously discussed as both NO reservoirs and as major actors in NO-dependent, but cGMP-independent, signal transduction. Although S-nitrosation of specific cysteine residues has been suggested to represent
Angelika B Riemer et al.
Experimental dermatology, 21(8), 625-629 (2012-07-11)
Based on the exquisite sensitivity, reproducibility and wide dynamic range of quantitative reverse-transcription real-time polymerase chain reaction (qRT-PCR), it is currently the gold standard for gene expression studies. Target gene expression is calculated relative to a stably expressed reference gene.
Kayla Baretta et al.
Acta crystallographica. Section F, Structural biology and crystallization communications, 68(Pt 7), 790-792 (2012-07-04)
Acinetobacter baumannii is a common multidrug-resistant clinical pathogen that is often found in hospitals. The A. baumannii phosphoglycerate kinase (AbPGK) is involved in the key energy-producing pathway of glycolysis and presents a potential target for antibiotic development. AbPGK has been
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