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2-Mercapto-4,5,6-triaminopyrimidine, commonly known as thiamine or thiamin, is an essential vitamin that plays a crucial role in the proper functioning of the human body. As a water-soluble compound, it is involved in various biochemical reactions, such as the metabolism of carbohydrates and energy production. Thiamine is also vital for the functioning of the nervous system and for maintaining healthy skin, hair, and nails. It can be found in a variety of foods, including whole grains, nuts, and meat, and is available as a dietary supplement. Thiamine deficiency can lead to serious health issues, such as beriberi and Wernicke-Korsakoff syndrome, emphasizing the importance of adequate thiamine intake through diet or supplementation.

1073-99-0

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1073-99-0 Usage

Uses

Used in Nutritional Supplements:
2-Mercapto-4,5,6-triaminopyrimidine is used as a dietary supplement to ensure adequate thiamine intake, particularly for individuals who may not consume enough of this essential vitamin through their diet. It helps support the proper functioning of the nervous system, energy production, and overall health.
Used in Food Fortification:
2-Mercapto-4,5,6-triaminopyrimidine is used as a fortifying agent in various food products to enhance their nutritional value and provide additional thiamine to consumers. This is particularly important for populations at risk of thiamine deficiency, such as those with limited access to a diverse diet or specific dietary restrictions.
Used in Pharmaceutical Applications:
2-Mercapto-4,5,6-triaminopyrimidine is used in the development of pharmaceutical formulations to treat thiamine deficiency-related conditions, such as beriberi and Wernicke-Korsakoff syndrome. It can also be incorporated into medications designed to support the nervous system and overall health.
Used in Research and Development:
2-Mercapto-4,5,6-triaminopyrimidine is utilized in scientific research to study its role in various biochemical processes and its potential applications in the development of new therapeutic agents and interventions for health-related conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 1073-99-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,7 and 3 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1073-99:
(6*1)+(5*0)+(4*7)+(3*3)+(2*9)+(1*9)=70
70 % 10 = 0
So 1073-99-0 is a valid CAS Registry Number.
InChI:InChI=1/C4H7N5S/c5-1-2(6)8-4(10)9-3(1)7/h5H2,(H5,6,7,8,9,10)

1073-99-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,5,6-triamino-1H-pyrimidine-2-thione

1.2 Other means of identification

Product number -
Other names 2(1H)-Pyrimidinethione,4,5,6-triamino

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:1073-99-0 SDS

1073-99-0Upstream product

1073-99-0Relevant articles and documents

Method for synthesis of adenine (by machine translation)

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Paragraph 0055; 0144; 0158; 0161, (2017/02/24)

The invention discloses a synthetic method for adenine. Malononitrile and thiourea are employed as raw materials. The raw materials are subjected to a cyclization reaction under action of sodium alkoxide, and 4,6-diamino-2-sulfydryl pyrimidine. Then through three reaction routes, adenine is obtained. Though the method has many reaction steps, no refining or drying are needed for the product of each reaction step, the product can be used in the next reaction step, and the operation is simple. The raw materials are easily available, the prices are relatively low, the reaction conditions are mild, the operation is simple, the reaction steps are decreased, the reaction time is shortened, the overall reaction yield is high, and the synthetic method is suitable for industrial production.

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