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3-Methyl-2-benzothiazolinone hydrazone hydrochloride hydrate, 97%, Thermo Scientific Chemicals

$89.59 - $967.04

Chemical Identifiers

CAS 149022-15-1
Molecular Formula C8H10ClN3S
Molecular Weight (g/mol) 215.70
MDL Number MFCD00149370
InChI Key OEZPVSPULCMUQB-UHFFFAOYSA-N
Synonym unii-9u2c4w7epr, mbth hydrochloride, 9u2c4w7epr, 3-methyl-2-benzothiazolone hydrazone hydrochloride, 3-methyl-2-benzothiazolinone hydrazone hydrochloride, z-2-hydrazono-3-methyl-2,3-dihydrobenzo d thiazole hydrochloride, mbth hcl, ccris 1543, 2 3h-benzothiazolone, 3-methyl-, hydrazone, hydrochloride 1:1, 2e-2-hydrazinylidene-3-methyl-1,3-benzothiazole hydrochloride
PubChem CID 9575839
IUPAC Name (Z)-(3-methyl-1,3-benzothiazol-2-ylidene)hydrazine;hydrochloride
SMILES Cl.CN1C(SC2=CC=CC=C12)=NN
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Products 3
Catalog Number Mfr. No. Quantity Price Quantity  
Catalog Number Mfr. No. Quantity Price Quantity  
AAA1631706
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Thermo Scientific Chemicals
A1631706
5 g
Each for $89.59
 
AAA1631714
SDS View Documents
Thermo Scientific Chemicals
A1631714
25 g
Each for $346.60
 
AAA1631722
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Thermo Scientific Chemicals
A1631722
100 g
Each for $967.04
 
Description

Description

3-Methyl-2-benzothiazolinone hydrazone hydrochloride hydrate is used in the synthesis of benzothiazolium azo dyes. It is a chromogenic reagent used for the determination of cholesterol, benzodiazepines and enzyme activity. As an electrophilic coupling reagent, it is used in the spectrophotometric determination of chloramine-B (CAB) and other residual chlorine content in various environmental water samples.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
3-Methyl-2-benzothiazolinone hydrazone hydrochloride hydrate is used in the synthesis of benzothiazolium azo dyes. It is a chromogenic reagent used for the determination of cholesterol, benzodiazepines and enzyme activity. As an electrophilic coupling reagent, it is used in the spectrophotometric determination of chloramine-B (CAB) and other residual chlorine content in various environmental water samples.

Solubility
Soluble in water, dimethyl sulfoxide and methanol.

Notes
Incompatible with strong oxidizing agents.
Specifications

Chemical Identifiers

149022-15-1
215.70
OEZPVSPULCMUQB-UHFFFAOYSA-N
9575839
Cl.CN1C(SC2=CC=CC=C12)=NN
C8H10ClN3S
MFCD00149370
unii-9u2c4w7epr, mbth hydrochloride, 9u2c4w7epr, 3-methyl-2-benzothiazolone hydrazone hydrochloride, 3-methyl-2-benzothiazolinone hydrazone hydrochloride, z-2-hydrazono-3-methyl-2,3-dihydrobenzo d thiazole hydrochloride, mbth hcl, ccris 1543, 2 3h-benzothiazolone, 3-methyl-, hydrazone, hydrochloride 1:1, 2e-2-hydrazinylidene-3-methyl-1,3-benzothiazole hydrochloride
(Z)-(3-methyl-1,3-benzothiazol-2-ylidene)hydrazine;hydrochloride

Specifications

149022-15-1
C8H10ClN3S
5 g
3571041
Soluble in water,dimethyl sulfoxide and methanol.
Cl.CN1C(SC2=CC=CC=C12)=NN
215.70
215.71 (Anhydrous)
3-Methyl-2-benzothiazolinone hydrazone hydrochloride hydrate
∼275°C (decomposition)
MFCD00149370
UN2811
unii-9u2c4w7epr, mbth hydrochloride, 9u2c4w7epr, 3-methyl-2-benzothiazolone hydrazone hydrochloride, 3-methyl-2-benzothiazolinone hydrazone hydrochloride, z-2-hydrazono-3-methyl-2,3-dihydrobenzo d thiazole hydrochloride, mbth hcl, ccris 1543, 2 3h-benzothiazolone, 3-methyl-, hydrazone, hydrochloride 1:1, 2e-2-hydrazinylidene-3-methyl-1,3-benzothiazole hydrochloride
OEZPVSPULCMUQB-UHFFFAOYSA-N
(Z)-(3-methyl-1,3-benzothiazol-2-ylidene)hydrazine;hydrochloride
9575839
97%
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Safety and Handling

Safety and Handling

GHS H Statement
H301
Toxic if swallowed.

P264b-P270-P301+P310-P330-P501c

H301

DOTInformation : Transport Hazard Class: 6.1; Packing Group: III; Proper Shipping Name: TOXIC SOLIDS, ORGANIC, N.O.S.

EINECSNumber : 238-428-7

RTECSNumber : DL7160200

TSCA : No

Recommended Storage : Ambient temperatures

SDS
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missing translation for 'documents'

RUO – Research Use Only