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Home > Encyclopedia > 5-Aminoimidazole-4-carboxamide hydrochloride

5-Aminoimidazole-4-carboxamide hydrochloride

pharmaceutical raw materials
5-Aminoimidazole-4-carboxamide hydrochloride structure

5-Aminoimidazole-4-carboxamide hydrochloride 

structure
  • CAS No:

    72-40-2

  • Formula:

    C4H6N4O.ClH

  • Chemical Name:

    5-Aminoimidazole-4-carboxamide hydrochloride

  • Synonyms:

    1H-Imidazole-4-carboxamide,5-amino-,hydrochloride (1:1);Imidazole-4-carboxamide,5-amino-,monohydrochloride;1H-Imidazole-4-carboxamide,5-amino-,monohydrochloride;4-Aminoimidazole-5-carboxamide hydrochloride;5-Aminoimidazole-4-carboxamide hydrochloride;4-Amino-5-carbamoylimidazole hydrochloride;5-Amino-1H-imidazole-4-carboxamide hydrochloride;1193-51-7

  • Categories:

    Pharmaceutical Intermediates  >  Bulk Drug Intermediates

Description

very slightly beige fine powder

5-Aminoimidazole-4-carboxamide hydrochloride Basic Attributes

162.58

162.030838

3701645

200-778-3

220691X0M3

113496

29332990

Characteristics

97.8

1.17430

White Crystals or Crystalline Powder

255-256 °C

522.1°C at 760 mmHg

269.6ºC

water: soluble 50mg/mL, clear, light yellow

Safety Information

NONH for all modes of transport

3

20/21/22-36/37/38

22-24/25-36-26

NI3911000

Xi,Xn

Irritant

P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, P501

H315

|Warning|H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]|P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, and P501|Aggregated GHS information provided by 4 companies from 2 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

5-Aminoimidazole-4-carboxamide hydrochloride Use and Manufacturing

Methods of Manufacturing

It is obtained from α-amidinoacetamide hydrochloride, aniline and formic acid as raw materials through diazotization, coupling, reduction, formylation and cyclization.

Uses

Pharmaceutical intermediates. Used in the production of nitrimidamine and acarbamine.

1H-Imidazole-4-carboxamide, 5-amino-, hydrochloride (1:1): INACTIVE

Computed Properties

Molecular Weight:162.58
Hydrogen Bond Donor Count:4
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:1
Exact Mass:162.0308386
Monoisotopic Mass:162.0308386
Topological Polar Surface Area:97.8
Heavy Atom Count:10
Complexity:126
Covalently-Bonded Unit Count:2
Compound Is Canonicalized:Yes

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