63730
2-Mercaptobenzothiazole
technical, ≥90% (T)
Synonym(s):
2-Benzothiazolethiol, MBT
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About This Item
Empirical Formula (Hill Notation):
C7H5NS2
CAS Number:
Molecular Weight:
167.25
Beilstein:
119484
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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grade
technical
Assay
≥90% (T)
form
solid
mp
177-181 °C (lit.)
SMILES string
Sc1nc2ccccc2s1
InChI
1S/C7H5NS2/c9-7-8-5-3-1-2-4-6(5)10-7/h1-4H,(H,8,9)
InChI key
YXIWHUQXZSMYRE-UHFFFAOYSA-N
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Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Aquatic Acute 1 - Aquatic Chronic 1 - Skin Sens. 1
Storage Class Code
11 - Combustible Solids
WGK
WGK 2
Flash Point(F)
392.0 °F - closed cup
Flash Point(C)
200 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Xu-Cheng Fu et al.
Analytica chimica acta, 685(1), 21-28 (2010-12-21)
This work reports a surface ion imprinting strategy in electropolymerized microporous poly(2-mercaptobenzothiazole) (MPMBT) films at the surface of glassy carbon electrode (GCE) for the electrochemical detection of Hg(II). The Hg(II)-imprinted MPMBT/GCE exhibits larger binding to functionalized capacity, faster binding kinetics
Kuan-Jen Chen et al.
Talanta, 81(4-5), 1670-1675 (2010-05-06)
This research reports a sensor array consisting of three types of surface-modified nanoparticles that exhibit localized surface plasmon resonance (LSPR) extinctions at different wavelength regions of a UV-vis spectrum. By simultaneously measuring the ensemble of the LSPR bands of the
N Pourreza et al.
Journal of hazardous materials, 178(1-3), 566-571 (2010-02-24)
A novel solid phase extractor for preconcentration of cadmium at ng L(-1) levels has been developed. Cadmium ions were retained on a column packed with sulfur powder modified with 2-mercaptobenzothiazole (2-MBT) in the medium of 1-butyl-3-methylimidazolium hexafluorophosphate ([bmim](+)PF(6)(-)) ionic liquid.
Itai Chipinda et al.
Chemical research in toxicology, 20(8), 1084-1092 (2007-07-17)
The rubber accelerator, 2-mercaptobenzothiazole (MBT), has been reported to cause allergic contact dermatitis from gloves and other rubber products, but its chemical fate when exposed to occupational oxidants and the mechanism of its pathogenesis are not known. It was hypothesized
Fei Wang et al.
Organic letters, 13(12), 3202-3205 (2011-05-20)
An efficient strategy for the synthesis of a variety of 2-mercaptobenzothiazole derivatives has been developed. The reaction proceeded from o-haloaniline derivatives and carbon disulfide via a tandem reaction in the presence of 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU) to afford the corresponding 2-mercaptobenzothiazole derivatives
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