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63730

2-Mercaptobenzothiazole

Name: 2-Mercaptobenzothiazole
Brand: ALDRICH

technical, ≥90% (T)

Synonym(s):

2-Benzothiazolethiol, MBT

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About This Item

Empirical Formula (Hill Notation):

C₇H₅NS₂

CAS Number:

149-30-4

Molecular Weight:

167.25

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

57651956

EC Number:

205-736-8

Beilstein/REAXYS Number:

119484

MDL number:

MFCD00005781

Assay:

≥90% (T)

Form:

solid

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Properties

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

Description

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pictograms

GHS07,GHS09

signalword

Warning

hcodes

H317,H410

pcodes

P261 - P272 - P273 - P280 - P302 + P352 - P333 + P313

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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Three-dimensional analysis of the change in the curvature of the smiling line following orthodontic treatment in incisor class II division 1 malocclusion.

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

Fast and efficient removal of mercury from water samples using magnetic iron oxide nanoparticles modified with 2-mercaptobenzothiazole.

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

Synthesis of 2-mercaptobenzothiazoles via DBU-promoted tandem reaction of o-haloanilines and carbon disulfide.

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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Global Trade Item Number

SKU	GTIN
63730-250G	04061832725895