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Tetrabutylthiuram Disulfide - >98.0%(N), high purity , CAS No.1634-02-2
Basic Description
Synonyms
DTXSID6049226 | E78822 | Bis(dibutylthiocarbamoyl) disulfide | Bis-(dibutylthiocarbamoyl) disulfide | BRN 1715575 | PGAXJQVAHDTGBB-UHFFFAOYSA-N | J-010042 | Zinc ionophore I | BDBM50570514 | THIOPEROXYDICARBONIC DIAMIDE (((H2N)C(S))2S2), N,N,N',N'- TETRAB
Specifications & Purity
≥98%(N)
Storage Temp
Argon charged
Shipped In
Normal
Taxonomic Classification
Kingdom
Organic compounds
Superclass
Organic nitrogen compounds
Class
Organonitrogen compounds
Subclass
Amines
Intermediate Tree Nodes
Tertiary amines
Direct Parent
Thiuram disulfides
Alternative Parents
Organic disulfides Sulfenyl compounds Organopnictogen compounds Hydrocarbon derivatives
Molecular Framework
Aliphatic acyclic compounds
Substituents
Thiuram disulfide - Organic disulfide - Sulfenyl compound - Organopnictogen compound - Hydrocarbon derivative - Organosulfur compound - Aliphatic acyclic compound
Description
This compound belongs to the class of organic compounds known as thiuram disulfides. These are organic disulfides that have the general structural formula RN(R')C(=S)SSC(=S)N(R\")R\"', where R-R\"'=alkyl groups.
External Descriptors
Not available
Data sources
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.
Associated Targets(Human)
Mechanisms of Action
Mechanism of Action
Action Type
target ID
Target Name
Target Type
Target Organism
Binding Site Name
References
Names and Identifiers
Pubchem Sid
488182119
Pubchem Sid Url
https://pubchem.ncbi.nlm.nih.gov/substance/488182119
IUPAC Name
dibutylcarbamothioylsulfanyl N,N-dibutylcarbamodithioate
INCHI
InChI=1S/C18H36N2S4/c1-5-9-13-19(14-10-6-2)17(21)23-24-18(22)20(15-11-7-3)16-12-8-4/h5-16H2,1-4H3
InChIKey
PGAXJQVAHDTGBB-UHFFFAOYSA-N
Smiles
CCCCN(CCCC)C(=S)SSC(=S)N(CCCC)CCCC
Isomeric SMILES
CCCCN(CCCC)C(=S)SSC(=S)N(CCCC)CCCC
RTECS
JO0800000
PubChem CID
15412
Molecular Weight
408.74
Reaxy-Rn
1715575
Certificates（CoA,COO,BSE/TSE and Analysis Chart)
Chemical and Physical Properties
Sensitivity
air sensitive
Refractive Index
1.58
Melt Point(°C)
33℃
Molecular Weight
408.800 g/mol
XLogP3
7.400
Hydrogen Bond Donor Count
0
Hydrogen Bond Acceptor Count
4
Rotatable Bond Count
15
Exact Mass
408.176 Da
Monoisotopic Mass
408.176 Da
Topological Polar Surface Area
121.000 Ų
Heavy Atom Count
24
Formal Charge
0
Complexity
289.000
Isotope Atom Count
0
Defined Atom Stereocenter Count
0
Undefined Atom Stereocenter Count
0
Defined Bond Stereocenter Count
0
Undefined Bond Stereocenter Count
0
The total count of all stereochemical bonds
0
Covalently-Bonded Unit Count
1
Citations of This Product
1.
Yanli Zhu, Jikai Wang, Haitao Xie, Hailing Liu, Shuangquan Liu, Dongxiu He, Pengbing Mi, Suisui He, Jun Wang, Yiyang Sun.
(2022)
NIR-to-Vis Handheld Platforms for Detecting miRNA Level and Mutation Based on Sub-10 nm Sulfide Nanodots and HCR Amplification. ACS Applied Materials & Interfaces,
14
(8):
(10212–10226).
2.
Ting Lü, Shuang Zhang, Dongming Qi, Dong Zhang, Hongting Zhao.
(2016)
Thermosensitive poly(N-isopropylacrylamide)-grafted magnetic nanoparticles for efficient treatment of emulsified oily wastewater. JOURNAL OF ALLOYS AND COMPOUNDS,
688
(513).
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2 Citations
D2112100