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2,4-Dimercapto-5,6-diaminopyrimidine is a chemical compound characterized by its two thiol (-SH) groups and two amine (-NH2) groups attached to a pyrimidine ring. It is recognized for its antifungal properties and is particularly effective against the fungus Malassezia furfur, which is a primary cause of dandruff.

31295-41-7

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31295-41-7 Usage

Uses

Used in Cosmetic and Personal Care Industry:
2,4-Dimercapto-5,6-diaminopyrimidine is used as an anti-dandruff agent in various cosmetic and personal care products, such as shampoos and scalp treatments. It is employed for its ability to control dandruff by targeting the fungus Malassezia furfur, thereby reducing flaking and itching associated with the condition.
2,4-Dimercapto-5,6-diaminopyrimidine works by interfering with the growth and reproduction of the fungus, which contributes to improved scalp health and a reduction in dandruff symptoms. Furthermore, 2,4-Dimercapto-5,6-diaminopyrimidine is valued for its low toxicity and minimal side effects, making it a safe and effective option for managing dandruff in personal care formulations.

Check Digit Verification of cas no

The CAS Registry Mumber 31295-41-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,2,9 and 5 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 31295-41:
(7*3)+(6*1)+(5*2)+(4*9)+(3*5)+(2*4)+(1*1)=97
97 % 10 = 7
So 31295-41-7 is a valid CAS Registry Number.
InChI:InChI=1/C4H6N4S2/c5-1-2(6)7-4(10)8-3(1)9/h5H2,(H4,6,7,8,9,10)

31295-41-7 Well-known Company Product Price

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  • Aldrich

  • (D15405)  4,5-Diamino-2,6-dimercaptopyrimidine  technical grade, 90%

  • 31295-41-7

  • D15405-5G

  • 1,339.65CNY

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31295-41-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 5,6-diamino-1H-pyrimidine-2,4-dithione

1.2 Other means of identification

Product number -
Other names 5,6-Diaminopyrimidine-2,4-dithiol

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:31295-41-7 SDS

31295-41-7Relevant academic research and scientific papers

N-Alkylation of 2,6-dichloropurine hydrochloride with a variety of alcohols over alumina catalyst

Tumma, Harikrishna,Nagaraju,Reddy, K. Vijayakumar

scheme or table, p. 1856 - 1866 (2010/07/02)

2,6-Dichloropurine hydrochloride reacts with various types of alcohols using different alumina catalysts and converts into its N-9-alkyl-2-chloro-6- hydroxy-9H-purine products to an extent of 49-74%. The product selectivity depends on the stability of carbocation generated from the alcohol. More stable carbocation formulates both N-7 and N-9-alkyl-2,6-dichloropurine products, whereas the less stable carbocation results in exclusively N-9-alkyl-2-chloro-6- hydroxy-9H-purine. The catalytic activity of alumina prepared using the sol-gel method has larger Brunauer, Emmett, and Teller (BET) surface area and hence shows significantly greater catalytic activity than the commercially available alumina samples. Copyright

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