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642436

Sigma-Aldrich

2-Hydrazinobenzothiazole

97%

Synonym(s):

Benzothiazol-2-yl-hydrazine

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About This Item

Empirical Formula (Hill Notation):
C7H7N3S
CAS Number:
615-21-4
Molecular Weight:
165.22
EC Number:
210-416-6
MDL number:
MFCD00041849
UNSPSC Code:
12352100
PubChem Substance ID:
24883194
NACRES:
NA.22

Quality Level

100

Assay

97%

form

solid

mp

198-202 °C (lit.)

functional group

hydrazine

SMILES string

NNc1nc2ccccc2s1

InChI

1S/C7H7N3S/c8-10-7-9-5-3-1-2-4-6(5)11-7/h1-4H,8H2,(H,9,10)

InChI key

JYSUYJCLUODSLN-UHFFFAOYSA-N

Pictograms

Skull and crossbones
GHS06

Signal Word

Danger

Hazard Statements

H301,H315,H319

Hazard Classifications

Acute Tox. 3 Oral - Eye Irrit. 2 - Skin Irrit. 2

Storage Class Code

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
MKCT8434
MKCG5333
MKBW3180V
MKBR6126V
MKBG3922V

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Lixiang Cheng et al.
BMC plant biology, 16(1), 188-188 (2016-09-01)
Drought stress is one of the most adverse environmental constraints to plant growth and productivity. Comparative proteomics of drought-tolerant and sensitive wheat genotypes is a strategy to understand the complexity of molecular mechanism of wheat in response to drought. This
Zhengyi Chen et al.
Analytica chimica acta, 1065, 29-39 (2019-04-22)
It remains a significant challenge for fast and high-throughput detection of trace analytes in complex samples with surface-enhanced Raman scattering (SERS) strategy due to the severe interference from matrices. In this work, a miniaturized array gas membrane separation (AGMS) device
M Beljean-Leymarie et al.
Analytical biochemistry, 173(1), 174-184 (1988-08-15)
A method for the measurement of malondialdehyde (MDA) using GLC with a nitrogen phosphorus detector (GLC/NPD) is described and evaluated. The method uses 2-hydrazinobenzothiazole (HBT) which forms condensation derivatives with MDA, acetoacetaldehyde, and acetylacetone (AA). GC/MS and 13C NMR studies

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