Tetramethylthiuram Monosulfide - ≥98%(GC) , CAS No.97-74-5

CAS: 97-74-5 Cat. No.: T161813 Molecular Weight: 208.36 EC Number: 202-605-7 PubChem CID: 7347
AVAILABLE TO ORDER
GRADE & PURITY ≥98%(GC)
Synonyms
Bis(dimethylaminethiocarbonyl)monosulfide | BISDIMETHYLTHIOCARBAMYL SULFIDE | Bis(dimethylthiocarbamyl) monosulfide | NSC4767 | NSC-4767 | Perkacit TMTM | s2432 | Tetramethyldithiocarbamic acid anhydrosulfide | Usaf B-32 | N,N,N',N'-Tetramethyldicarbonotr
Storage
Room temperature
Shipped In
Normal
 ·  off list, applied to all prices below.
Size
Status
Price
Qty
5g
T161813-5g
2

$9.90

$14.90
Save $5.00 (33.56%)
25g
T161813-25g
2

$11.90

$17.90
Save $6.00 (33.52%)
100g
T161813-100g
1

$20.90

$31.90
Save $11.00 (34.48%)
250g
T161813-250g
3

$45.90

$68.90
Save $23.00 (33.38%)
500g
T161813-500g
1

$65.90

$98.90
Save $33.00 (33.37%)
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Why this grade

≥98%(GC) for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Room temperature Ships Normal Check lot-specific COA for exact specifications.

📋

Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 1 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Synonyms
Bis(dimethylaminethiocarbonyl)monosulfide | BISDIMETHYLTHIOCARBAMYL SULFIDE | Bis(dimethylthiocarbamyl) monosulfide | NSC4767 | NSC-4767 | Perkacit TMTM | s2432 | Tetramethyldithiocarbamic acid anhydrosulfide | Usaf B-32 | N, N, N', N'-Tetramethyldicarbonotr
Specifications & Purity
≥98%(GC)
Storage
Room temperature
Shipped In
Normal
Purity
≥98%(GC)
Names and Identifiers
Pubchem Sid504751310
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504751310
Canonical SmilesCN(C)C(=S)SC(=S)N(C)C
IUPAC Namedimethylcarbamothioyl N,N-dimethylcarbamodithioate
InChIKeyREQPQFUJGGOFQL-UHFFFAOYSA-N
INCHI1S/C6H12N2S3/c1-7(2)5(9)11-6(10)8(3)4/h1-4H3
Isomeric SMILES CN(C)C(=S)SC(=S)N(C)C
WGK Germany 3
RTECS WQ1750000
PubChem CID 7347
Molecular Weight 208.36
Reaxy-Rn 1775650

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganosulfur compounds
ClassSulfenyl compounds
SubclassNot available
Intermediate Tree Nodes Not available
Direct ParentSulfenyl compounds
Alternative Parents Organopnictogen compounds  Organonitrogen compounds  Hydrocarbon derivatives  
Molecular FrameworkAliphatic acyclic compounds
Substituents Sulfenyl compound - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Organonitrogen compound - Aliphatic acyclic compound
DescriptionThis compound belongs to the class of organic compounds known as sulfenyl compounds. These are organosulfur compounds a sulfenyl group with the general formula RS (R = organyl).
External Descriptors Not available
3D Structure
Interactive Chemical Structure Model





Associated Targets(Human)
NR3C1 Tclin Glucocorticoid receptor (14987 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
AR Tclin Androgen Receptor (11781 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
VDR Tclin Vitamin D receptor (26531 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ALDH1A1 Tchem Aldehyde dehydrogenase 1A1 (77053 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HeLa (62764 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MGLL Tchem Monoglyceride lipase (1909 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HTT Tchem Huntingtin (19182 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
EHMT2 Tchem Histone-lysine N-methyltransferase, H3 lysine-9 specific 3 (93046 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
TDP1 Tchem Tyrosyl-DNA phosphodiesterase 1 (345557 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
LMNA Tbio Prelamin-A/C (36751 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
GMNN Tbio Geminin (128009 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PMP22 Tbio Peripheral myelin protein 22 (699 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Associated Targets(non-human)
Hdac6 Histone deacetylase 6 (222 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Faah Anandamide amidohydrolase (3907 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Plasmodium falciparum (966862 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Cryptococcus neoformans (21258 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Candida albicans (78123 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Nakaseomyces glabratus (9108 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Candida parapsilosis (8521 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Trichomonas vaginalis (2376 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Sporothrix schenckii (1580 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
GCN5 Histone acetyltransferase GCN5 (89 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Luciferin 4-monooxygenase (66902 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
rep Replicase polyprotein 1ab (378 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ddn Putative uncharacterized protein (49 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Trichophyton mentagrophytes (4846 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Nfe2l2 Nuclear factor erythroid 2-related factor 2 (214 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Rorc Nuclear receptor ROR-gamma (89407 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
fba Putative fructose-1,6-bisphosphate aldolase (15559 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ffp 4'-phosphopantetheinyl transferase ffp (24982 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mechanisms of Action
Certificates(CoA,COO,BSE/TSE and Analysis Chart)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

7 results found

Lot NumberCertificate TypeDateItem
A2621100Certificate of AnalysisJan 29, 2026 T161813
A2614100Certificate of AnalysisJan 21, 2026 T161813
L2525036Certificate of AnalysisDec 31, 2025 T161813
C2511183Certificate of AnalysisMar 15, 2025 T161813
I1916046Certificate of AnalysisJul 07, 2023 T161813
E2330109Certificate of AnalysisJun 09, 2023 T161813
G2426151Certificate of AnalysisJun 09, 2023 T161813
Chemical and Physical Properties
SolubilityVery soluble in Benzene,Chloroform,Acetone; Slightly soluble in Ether
Flash Point(°F)312.8 °F
Flash Point(°C)156 °C
Melt Point(°C)110 °C
Molecular Weight208.400 g/mol
XLogP31.700
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count3
Rotatable Bond Count2
Exact Mass208.016 Da
Monoisotopic Mass208.016 Da
Topological Polar Surface Area96.000 Ų
Heavy Atom Count11
Formal Charge0
Complexity147.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Citations of This Product
References
1. Liu Yatao, An Yun, Fang Chi, Ye Yaokun, An Yifeng, He Mengxue, Jia Yongfeng, Hong Xufeng, Liu Yumei, Gao Song, Hao Yizhou, Chen Jianhao, Zheng Jiaxin, Lu Yunfeng, Zou Ruqiang, Pang Quanquan.  (2025)  Surface-localized phase mediation accelerates quasi-solid-state reaction kinetics in sulfur batteries.  Nature Chemistry,      [PMID:39948281] [10.1038/s41557-025-01735-w]
Solution Calculators
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