M3302
2-Mercaptobenzothiazole
97%
Synonym(s):
2-Benzothiazolethiol, MBT
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About This Item
Empirical Formula (Hill Notation):
C7H5NS2
CAS Number:
Molecular Weight:
167.25
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
205-736-8
Beilstein/REAXYS Number:
119484
MDL number:
Product Name
2-Mercaptobenzothiazole, 97%
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
SMILES string
Sc1nc2ccccc2s1
assay
97%
mp
177-181 °C (lit.)
Quality Level
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Application
2-Mercaptobenzothiazole (MBT) has been used in the synthesis of MBT functionalized mesoporous silica which can be used as an adsorbent for the removal of Hg(II) from aqueous solution.
It can also be used as a:
It can also be used as a:
- Reference compound in photocatalytic activity tests under UV or visible light irradiation.
- Starting material for the synthesis of conjugates of 2-MBT for antitubercular activity studies.
- Starting material for the synthesis of 4-thiazolidinones.
signalword
Warning
hcodes
Hazard Classifications
Aquatic Acute 1 - Aquatic Chronic 1 - Skin Sens. 1
Storage Class
11 - Combustible Solids
wgk
WGK 2
flash_point_f
392.0 °F - closed cup
flash_point_c
200 °C - closed cup
ppe
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
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Preparation of 2-mercaptobenzothiazole-derivatized mesoporous silica and removal of Hg (II) from aqueous solution
Perez-Quintanilla D, et al.
Journal of Environmental Monitoring, 8(1), 214-222 (2006)
Michael Mah et al.
European journal of orthodontics, 36(6), 657-664 (2013-06-19)
To investigate the different effects of changes in the occlusal plane, incisors inclination, and maxillary intercanine width on the curvature of the smiling line. Records of 46 subjects (28 females and 18 males, mean age 16.6 ± 4.2 years) with
H Parham et al.
Journal of hazardous materials, 205-206, 94-100 (2012-01-17)
Mercury in the lowest levels of concentrations is dangerous for human health due to its bioaccumulation in body and toxicity. This investigation shows the effective removal of mercury (II) ions from contaminated surface waters by modified magnetic iron oxide nanoparticles
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
Enhanced photocatalytic activity of Ce3+?TiO2 for 2-mercaptobenzothiazole degradation in aqueous suspension for odour control
Li FB, et al.
Applied Catalysis, 285(1-2), 181-189 (2005)
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