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37847-87-3

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37847-87-3 Usage

Physical state

White solid

Uses

a. Cross-linking agent in rubber production
b. Antioxidant in rubber and plastic industries
c. Production of dyes and pharmaceuticals

Thermal stability

High degree of thermal stability

Effectiveness

Prevents degradation in rubber and plastic materials

Potential applications

Studied for its potential as an anti-tumor agent due to its ability to inhibit the growth of cancer cells

Safety precautions

Known to be an irritant to the skin, eyes, and respiratory system; should be handled with care

Check Digit Verification of cas no

The CAS Registry Mumber 37847-87-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,8,4 and 7 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 37847-87:
(7*3)+(6*7)+(5*8)+(4*4)+(3*7)+(2*8)+(1*7)=163
163 % 10 = 3
So 37847-87-3 is a valid CAS Registry Number.

37847-87-3SDS

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 1,1'-Dithiobis(N-phenylformamidine)

1.2 Other means of identification

Product number -
Other names -

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:37847-87-3 SDS

37847-87-3Upstream product

37847-87-3Downstream Products

37847-87-3Relevant articles and documents

Kinetics of electron transfer between bis(2,2'-bipyridine)manganese(III)complex and thioureas in aqueous perchlorate media

Ali, Mahammad,Gangopadhyay, Sumana,Dutta, Amitava,Banerjee, Pradyot

, p. 43 - 46 (2007/10/02)

Kinetics of the redox interactions of thiourea and its N-substituted derivatives with manganese(III) complex of 2,2'-bipyridine has been investigated in aqueous solution by stopped-flow technique in the acid range +>, 0.10-0.50 mol dm-3 at I=1.0 mol dm-3 (NaClO4) and at 30 deg C.A rapid initial increase in absorbance is followed by a slower decay of the formed species for all the four thioureas.Both the reaction steps are analysed and an inner sphere mechanism has been proposed for these reactions.The reactivity order for these thiourea derrivatives is: ptu>tu>mtu>atu, and this bears a consequence to their substituent effects.

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