P-Toluenesulfonylhydrazide (TSH) CAS 1576-35-8 for Organic Synthesis

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Package type
25kg/drum
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Customization: Available
CAS No.: 1576-35-8
Formula: C7h10n2o2s
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  • P-Toluenesulfonylhydrazide (TSH) CAS 1576-35-8 for Organic Synthesis
  • P-Toluenesulfonylhydrazide (TSH) CAS 1576-35-8 for Organic Synthesis
  • P-Toluenesulfonylhydrazide (TSH) CAS 1576-35-8 for Organic Synthesis
  • P-Toluenesulfonylhydrazide (TSH) CAS 1576-35-8 for Organic Synthesis
  • P-Toluenesulfonylhydrazide (TSH) CAS 1576-35-8 for Organic Synthesis
  • P-Toluenesulfonylhydrazide (TSH) CAS 1576-35-8 for Organic Synthesis
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Overview

Basic Info.

Model NO.
QMAX25257
EINECS
216-407-3
Type
Synthesis Material Intermediates
Appearance
Powder
Quality
Refined
Colour
White
Synonym1
4-Methylbenzenesulfonhydrazide
Synonym 2
P-Toluenesulfonylhydrazide
Abbreviation
Tsh
Sample
Available
Delivery
3-5days
Boiling Point
340.5±35.0 °C
Density
1.42
Storage
Store Below +30°C.
Burning Residue
≤0.5%
Solubility
139g/L
Melting Point
103-108°C
Sample Package
100g; 1kg; 25g
Supply Type
OEM/ODM
Certificate
ISO 9001
Moisture
≤0.5%
Transport Package
25kg/Bag; 25kg/Drum
Specification
99%
Trademark
QINMU
Origin
China
HS Code
2928000090
Production Capacity
300mt/Month

Product Description

P-Toluenesulfonylhydrazide (TSH) CAS 1576-35-8 for Organic Synthesis
Product Description

1.Basic Information for p-Toluenesulfonylhydrazide ( TSH ) CAS 1576-35-8:

1. Chemical Identification
IUPAC Name: 4-Methylbenzenesulfonohydrazide
Common Names:
p-Toluenesulfonylhydrazide
TSH (common abbreviation)
Tosylhydrazide
CAS Number: 1576-35-8
Molecular Weight: 186.23 g/mol

2. Physical & Chemical Properties
Appearance: White to off-white, crystalline powder.
Melting Point: ~110 - 113 °C (with decomposition)
Solubility: Slightly soluble in water; soluble in polar organic solvents (e.g., DMF, DMSO); sparingly soluble in alcohols; insoluble in non-polar solvents.

Reactivity: A versatile reagent. It acts as a source of hydrazine and a nucleophile. Key reactions include:

Wolff-Kishner-type Reduction: Forms hydrazones with aldehydes/ketones, which upon base treatment reduce the carbonyl to a methylene group.

Bamford-Stevens Reaction: Generates diazo compounds and subsequently carbenes or alkenes.

Decomposition: Upon heating above its melting point, it decomposes to release nitrogen gas, making it useful as a blowing agent.

Stability: Stable at room temperature but may decompose upon prolonged heating or exposure to strong acids/bases.

Item Specifications
Appearance  White crystalline powder
Titr content ( %) 98.0Min
Decomposed temp. 143-147 Min
Heating loss ( %) 0.5Max
Ash( %) 0.1Max
Gas yield   (ml/g) 120-130
PH 5.0~7.5
 
Product Parameters

2. p-Toluenesulfonylhydrazide ( TSH ) CAS 1576-35-8 Primary Application Fields:
Primary Function 1: Organic Synthesis Reagent. A valuable reagent for the reductive deoxygenation of carbonyl groups (via in situ hydrazone formation) and for the synthesis of alkenes and carbenes.

Primary Function 2: Chemical Blowing Agent. Its controlled thermal decomposition releases nitrogen gas, making it an effective endothermic blowing agent for producing foamed plastics and rubbers (e.g., PVC, EVA).

Other Uses: Used in polymer modification and as an intermediate in synthesis.
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P-Toluenesulfonylhydrazide (TSH) CAS 1576-35-8 for Organic Synthesis


P-Toluenesulfonylhydrazide (TSH) CAS 1576-35-8 for Organic SynthesisP-Toluenesulfonylhydrazide (TSH) CAS 1576-35-8 for Organic SynthesisP-Toluenesulfonylhydrazide (TSH) CAS 1576-35-8 for Organic Synthesis

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