Details
Stereochemistry | ACHIRAL |
Molecular Formula | C6H12N2S3 |
Molecular Weight | 208.368 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CN(C)C(=S)SC(=S)N(C)C
InChI
InChIKey=REQPQFUJGGOFQL-UHFFFAOYSA-N
InChI=1S/C6H12N2S3/c1-7(2)5(9)11-6(10)8(3)4/h1-4H3
DescriptionSources: http://www.chemotechnique.se/get_pdf.php?l=en&p=263
Sources: http://www.chemotechnique.se/get_pdf.php?l=en&p=263
Tetramethylthiuram monosulfide (TMTM) is used as a secondary accelerator and activator in the processing of natural and butyl rubbers. It is used as a fungicide, and insecticide.
Approval Year
PubMed
Title | Date | PubMed |
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Allergic contact dermatitis from natural latex. | 2001 Sep |
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[Preparation and catalysis capability of single crystal Co(C3H6NS2)3 x C6H12N2S3]. | 2008 Dec |
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Contact allergy to thiurams: multifactorial analysis of clinical surveillance data collected by the IVDK network. | 2010 Aug |
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Dithiocarbamates induce craniofacial abnormalities and downregulate sox9a during zebrafish development. | 2010 Sep |
Sample Use Guides
In Vivo Use Guide
Sources: http://www.ncbi.nlm.nih.gov/pubmed/2988157
adult female Wistar rats were administrated by gavage of tetramethyl thiurammonosulfide (TMTM, 2 mmol/kg)
Route of Administration:
Intragastric
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N0000185508
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N0000171131
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N0000184306
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N0000175629
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PRIMARY | Increased Histamine Release [PE] | ||
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1363713
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100000134279
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Tetramethylthiuram sulfide
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ACTIVE MOIETY