Sign In to View Organizational & Contract Pricing.
Select a Size
Change View
About This Item
Empirical Formula (Hill Notation):
C8H9N3S · HCl · xH2O
CAS Number:
Molecular Weight:
215.70 (anhydrous basis)
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
238-428-7
MDL number:
Assay:
97%
Form:
solid
assay
97%
form
solid
mp
276-278 °C (dec.) (lit.)
SMILES string
Cl[H].[H]O[H].CN1\C(Sc2ccccc12)=N\N
InChI
1S/C8H9N3S.ClH.H2O/c1-11-6-4-2-3-5-7(6)12-8(11)10-9;;/h2-5H,9H2,1H3;1H;1H2/b10-8-;;
InChI key
IYXXQOGEFHAQGU-GPWRMYTLSA-N
Application
Chromogenic reagent for the determination of benzodiazepines, cholesterol, and enzyme activity. Used in the synthesis of benzothiazolium azo dyes.
3-Methyl-2-benzothiazolinone hydrazone hydrochloride hydrate (MBTH hydrochloride hydrate) was used as an electrophilic coupling reagent for the determination of residual chlorine.
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 3 Oral - Eye Irrit. 2
Storage Class
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
wgk
WGK 3
ppe
Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Indian J. Chem. B, 32, 44-44 (1993)
J N Rodríguez-López et al.
Analytical biochemistry, 216(1), 205-212 (1994-01-01)
A continuous spectrophotometric method for the rapid determination of monophenolase activity of tyrosinase is described. This method is based on the coupling reaction between 3-methyl-2-benzothiazolinone hydrazone (MBTH) and the quinone products of the oxidation of various monophenols in the presence
Dyes and Pigments, 21, 159-159 (1993)
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 129739-5G | 04061838726506 |
| 129739-25G | 04061838726490 |
| 129739-100G | 04061838726483 |
