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10396-10-8

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10396-10-8 Usage

Chemical Properties

Fine, white powder.

Uses

Different sources of media describe the Uses of 10396-10-8 differently. You can refer to the following data:
1. Blowing Agent RA is high temperature foaming agent, so it's especially suitable for high temperature processing plastic. As a foaming agent, it can be used to produce synthetic rubber,for example:Hard PVC, High density polyethylene, polypropylene, polycarbonate, nylon, ABS, natural rubber, SBR,etc. The processing of this product is safe,and without the risk of foam in advance. Adding some active agent, it's suitable for low temperature foaming agent, for example: after using urea of surface treatment,it can reduce decomposition temperature.
2. p-toluenesulfonyl semicarbazide is high-temperature N2 blowing agent .It can particularly used in high-temperature processing plastic such as ABS resin ,nylon,hard PVC ,HIDE,polypropylene,polycarbonate etc.

Check Digit Verification of cas no

The CAS Registry Mumber 10396-10-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,3,9 and 6 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 10396-10:
(7*1)+(6*0)+(5*3)+(4*9)+(3*6)+(2*1)+(1*0)=78
78 % 10 = 8
So 10396-10-8 is a valid CAS Registry Number.
InChI:InChI=1/C8H11N3O3S/c1-6-2-4-7(5-3-6)15(13,14)11-10-8(9)12/h2-5,11H,1H3,(H3,9,10,12)

10396-10-8 Well-known Company Product Price

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  • (Code)Product description
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  • Alfa Aesar

  • (H61949)  p-Toluenesulfonyl semicarbazide, 95%   

  • 10396-10-8

  • 25g

  • 542.0CNY

  • Detail
  • Alfa Aesar

  • (H61949)  p-Toluenesulfonyl semicarbazide, 95%   

  • 10396-10-8

  • 100g

  • 1946.0CNY

  • Detail

10396-10-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name p-Toluenesulfonylsemicarbazide

1.2 Other means of identification

Product number -
Other names [(4-methylphenyl)sulfonylamino]urea

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:10396-10-8 SDS

10396-10-8Synthetic route

hydrazine carboxamide
4426-72-6, 51433-48-8

hydrazine carboxamide

p-toluenesulfonyl chloride
98-59-9

p-toluenesulfonyl chloride

N4-(4-Toluenesulfonyl)semicarbazide
10396-10-8

N4-(4-Toluenesulfonyl)semicarbazide

Conditions
ConditionsYield
aluminum oxide for 0.25h;83%
With potassium carbonate In tetrahydrofuran; methanol Acylation;
Azodicarboxamid
123-77-3

Azodicarboxamid

sodium 4-methylbenzenesulfinate
824-79-3

sodium 4-methylbenzenesulfinate

N4-(4-Toluenesulfonyl)semicarbazide
10396-10-8

N4-(4-Toluenesulfonyl)semicarbazide

Conditions
ConditionsYield
In dimethyl sulfoxide
C9H9Cl3N2O4S

C9H9Cl3N2O4S

N4-(4-Toluenesulfonyl)semicarbazide
10396-10-8

N4-(4-Toluenesulfonyl)semicarbazide

Conditions
ConditionsYield
With ammonium chloride; N-ethyl-N,N-diisopropylamine In tetrahydrofuran at 20℃; for 0.166667h;
1,4-butanediol bis(chloroformate)
2157-16-6

1,4-butanediol bis(chloroformate)

N4-(4-Toluenesulfonyl)semicarbazide
10396-10-8

N4-(4-Toluenesulfonyl)semicarbazide

C22H28N6O10S2
60226-44-0

C22H28N6O10S2

Conditions
ConditionsYield
With potassium hydroxide
N4-(4-Toluenesulfonyl)semicarbazide
10396-10-8

N4-(4-Toluenesulfonyl)semicarbazide

chloroformic acid ethyl ester
541-41-3

chloroformic acid ethyl ester

C11H15N3O5S
60226-46-2

C11H15N3O5S

Conditions
ConditionsYield
With potassium hydroxide
N4-(4-Toluenesulfonyl)semicarbazide
10396-10-8

N4-(4-Toluenesulfonyl)semicarbazide

isopropyl chloroformate
108-23-6

isopropyl chloroformate

1-p-Toluenesulfonyl-1-Carbisopropoxy-2-Carbamyl Hydrazine
60226-36-0

1-p-Toluenesulfonyl-1-Carbisopropoxy-2-Carbamyl Hydrazine

Conditions
ConditionsYield
With potassium hydroxide
N4-(4-Toluenesulfonyl)semicarbazide
10396-10-8

N4-(4-Toluenesulfonyl)semicarbazide

acrylonitrile
107-13-1

acrylonitrile

N,N,N'-Tris-(2-cyan-aethyl)-N'-p-toluolsulfonylhydrazin
16019-18-4

N,N,N'-Tris-(2-cyan-aethyl)-N'-p-toluolsulfonylhydrazin

Conditions
ConditionsYield
With triethylamine In water
N4-(4-Toluenesulfonyl)semicarbazide
10396-10-8

N4-(4-Toluenesulfonyl)semicarbazide

methyl chloroformate
79-22-1

methyl chloroformate

C10H13N3O5S
60226-45-1

C10H13N3O5S

Conditions
ConditionsYield
With potassium hydroxide
N4-(4-Toluenesulfonyl)semicarbazide
10396-10-8

N4-(4-Toluenesulfonyl)semicarbazide

carbonochloridic acid, butyl ester
592-34-7

carbonochloridic acid, butyl ester

C13H19N3O5S
60226-47-3

C13H19N3O5S

Conditions
ConditionsYield
With potassium hydroxide
N4-(4-Toluenesulfonyl)semicarbazide
10396-10-8

N4-(4-Toluenesulfonyl)semicarbazide

phenyl chloroformate
1885-14-9

phenyl chloroformate

C15H15N3O5S
60226-49-5

C15H15N3O5S

Conditions
ConditionsYield
With potassium hydroxide
N4-(4-Toluenesulfonyl)semicarbazide
10396-10-8

N4-(4-Toluenesulfonyl)semicarbazide

isobutyl chloroformate
543-27-1

isobutyl chloroformate

C13H19N3O5S
60226-48-4

C13H19N3O5S

Conditions
ConditionsYield
With potassium hydroxide
ammonium hydroxide
1336-21-6

ammonium hydroxide

N4-(4-Toluenesulfonyl)semicarbazide
10396-10-8

N4-(4-Toluenesulfonyl)semicarbazide

isopropyl chloroformate
108-23-6

isopropyl chloroformate

1-p-Toluenesulfonyl-1-Carbisopropoxy-2-Carbamyl Hydrazine
60226-36-0

1-p-Toluenesulfonyl-1-Carbisopropoxy-2-Carbamyl Hydrazine

Conditions
ConditionsYield
With potassium hydroxide In water

10396-10-8Relevant articles and documents

A convenient procedure for the preparation of sulfonamidoureas using triphosgene

Safaei-Ghomi, Javad,Bamoniri, Abdolhamid,Abbaszadeh-Nooshabady, Aboalfazl

, p. 721 - 724 (2008/10/09)

An efficient method for the preparation of sulfonamidourea using triphosgene in organic solvents is reported. Sulfonylhydrazides and acetylsulfanilylhydrazide were transformed into the corresponding intermediates using triphosgene in 1,4-dioxane/water or tetrahydrofuran as solvents. These intermediates were converted in situ into symmetrical and unsymmetrical sulfonamidoureas in high yields and shorter periods of time related to previous methods.

CARBONIC ANHYDRASE INHIBITORS. 9. INHIBITORS WITH MODIFIED SULFONAMIDO GROUPS AND THEIR INTERACTION WITH THE ZINC ENZYME

Supuran, Claudiu T.,Banciu, Mircea D.

, p. 1345 - 1354 (2007/10/03)

A number of 20 compounds, containing modified sulfonamido groups were prepared and tested as carbonic anhydrase inhibitors on the bovine enzyme. Novel classes of inhibitors were evidenced, and a new mode of binding for bidentate inhibitors was proposed, both for the native and Co(II) substituted enzyme.

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