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932-15-0

5-amino-3H-imidazole-4-carboxamide, also known as histamine, is a naturally occurring organic compound that plays a crucial role in various physiological processes. It is a derivative of imidazole, with an amino group at the 5th position and a carboxamide group at the 4th position. Histamine is primarily produced in the body by the decarboxylation of histidine, an essential amino acid. It acts as a neurotransmitter and a signaling molecule, involved in immune responses, gastric acid secretion, and the regulation of blood flow. Histamine is also known for its role in allergic reactions and inflammation, as it triggers the release of inflammatory mediators and increases vascular permeability. In addition to its physiological functions, histamine has been studied for its potential therapeutic applications, such as in the treatment of gastric ulcers and as a component in some anti-cancer therapies.

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  • 932-15-0 Structure

  • Basic information

    1. Product Name: 5-amino-3H-imidazole-4-carboxamide
    2. Synonyms: 5-AMINO-3H-IMIDAZOLE-4-CARBOXAMIDE;4-Carbamoyl-5-aminoimidazole;4-Carboxamido-5-aminoimidazole;5-Aminoimidazol-4-carboxamide;5-Aminoimidazole carboxamide;5-Aminoimidazolecarboxamide
    3. CAS NO:932-15-0
    4. Molecular Formula: C4H6N4O
    5. Molecular Weight: 126.12
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 932-15-0.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 5-amino-3H-imidazole-4-carboxamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: 5-amino-3H-imidazole-4-carboxamide(932-15-0)
    11. EPA Substance Registry System: 5-amino-3H-imidazole-4-carboxamide(932-15-0)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 932-15-0(Hazardous Substances Data)

932-15-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 932-15-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,3 and 2 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 932-15:
(5*9)+(4*3)+(3*2)+(2*1)+(1*5)=70
70 % 10 = 0
So 932-15-0 is a valid CAS Registry Number.

932-15-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1H-Imidazole-4-carboxamide, 5-amino-

1.2 Other means of identification

Product number -
Other names 4-Amino-5-carbamoylimidazole

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:932-15-0 SDS

932-15-0Upstream product

932-15-0Relevant articles and documents

Industrial production method of 4-amino-5-imidazolecarboxamide

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Paragraph 0040; 0045-0048; 0049; 0054, (2020/07/15)

The invention discloses an industrial production method of 4-amino-5-imidazolecarboxamide, belonging to the technical field of organic synthesis. The industrial production method comprises the following steps: S1, reacting diaminomaleonitrile with formamide under the action of phosphorus oxychloride to generate an intermediate 1; and S2, subjecting the intermediate 1 to a ring closing reaction under an alkaline condition so as to generate 4-amino-5-imidazolecarboxamide. The method has the advantages of simple raw materials, low price, short reaction steps, short production period, simple operation and easy realization of industrial production, avoids the generation of cyano-containing wastewater, nitrogen-containing wastewater and the like in traditional synthesis methods, causes very small environmental protection pressure, and realizes preparation of the high-quality 4-amino-5-imidazolecarboxamide only through two reactions.

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