4-Amino-5-imidazolecarboxamide hydrochloride CAS 72-40-2

Introduction:Basic information about 4-Amino-5-imidazolecarboxamide hydrochloride CAS 72-40-2, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.

4-Amino-5-imidazolecarboxamide hydrochloride Basic information

Product Name:4-Amino-5-imidazolecarboxamide hydrochloride
Synonyms:5-amino-4-imidazolecarboxamide hydrochloride (intermediate of dacarbazine);5-Amino-1H-imidazole-4-carboxamide hydrochloride 98%;5-amino-1H-imidazole-4-carboxamide HCl;4-Amino-5-(aminocarbonyl)imidazole Hydrochloride;4-AMINO-5-IMIDAZOLECARBOXAMIDE HCL, (AICA) 98+%;4-AMINO-5-IMIDAZOLECARBOXAMIDE HYDROCHLORIDE 99%;4-Amino-5-imidazolecarboxamide hydrochloride ,99%;4-Amino-5-imidazolecarboxamide hydrochloride,98%
CAS:72-40-2
MF:C4H7ClN4O
MW:162.58
EINECS:200-778-3
Product Categories:Imidazoles, Pyrroles, Pyrazoles, Pyrrolidines;pharmacetical;Imidazoles;(intermediate of dacarbazine)
Mol File:72-40-2.mol

4-Amino-5-imidazolecarboxamide hydrochloride Chemical Properties

Melting point 250-252 °C (dec.)(lit.)
storage temp. 2-8°C
solubility water: soluble50mg/mL, clear, light yellow
form Crystals or Crystalline Powder
color White
Water Solubility SOLUBLE
Sensitive Hygroscopic
BRN 3701645
Stability:Hygroscopic
InChIInChI=1S/C4H6N4O.ClH/c5-3-2(4(6)9)7-1-8-3;/h1H,5H2,(H2,6,9)(H,7,8);1H
InChIKeyMXCUYSMIELHIQL-UHFFFAOYSA-N
SMILESC1(N=CNC=1N)C(=O)N.Cl
CAS DataBase Reference72-40-2(CAS DataBase Reference)
NIST Chemistry ReferenceImidazole-4(5)-carboxamide, 5-(4)-amino-, hydrochloride(72-40-2)
EPA Substance Registry System1H-Imidazole-4-carboxamide, 5-amino-, monohydrochloride (72-40-2)

Safety Information

Hazard Codes Xi,Xn
Risk Statements 20/21/22-36/37/38
Safety Statements 22-24/25-36-26
WGK Germany 3
RTECS NI3911000
Hazard Note Irritant
TSCA TSCA listed
HS Code 29332990
Storage Class11 - Combustible Solids

4-Amino-5-imidazolecarboxamide hydrochloride Usage And Synthesis

Chemical Propertiesvery slightly beige fine powder
Uses5-Amino-4-imidazolecarboxamide hydrochloride was used in the synthesis of heterocyclic compounds such as guanine, purines and pyrimidines.
General DescriptionCorrosion inhibition and adsorption characteristics of 5-amino-4-imidazolecarboxamide hydrochloride on aluminum in 1M HCl has been investigated.
Synthesis47 g of sodium nitrite was dissolved in 1.2 liters of water; The solution was cooled to 0° C. 100 g of 5-aminoimidazole-4 carboxamide was dissolved in a solution of hydrochloric acid (80 ml of 36% HCL in 720 ml water) with stirring. The resultant 5-aminoimidazole-4 carboxamide hydrochloride solution was added slowly, drop-wise, over 20-30 minutes at 0-5° C. After the addition was completed, the reaction mixture was stirred for 10 minutes and filtered. The solid obtained was suspended in 400 ml DM water and stirred for 15 minutes. The suspension was filtered and suction-dried for 15 minutes. The obtained solid was suspended in 500 ml of THF and stirred for 15 minutes. The suspension was filtered and suction-dried for 15 minutes. Finally, the solid was dried at 45° C. to afford 4-Amino-5-imidazolecarboxamide hydrochloride.
Purification MethodsRecrystallise the hydrochloride from EtOH. [Kuroda & Hakko JEst(1) Est(2)Heterocycl Chem 30 593 1993, Alhede et al. J Org Chem 56 2139 1991, Cheru et al. Heterocycles 24 1133 1992, Beilstein 25 II 221, 25 III/IV 4329.]

4-Amino-5-imidazolecarboxamide hydrochloride Preparation Products And Raw materials

Raw materialsAcetamide-->carbanilic acid
Preparation Products5-(Amino-1-(N-methyl Carbamoyl)-->ETHYL 4-AMINO-5-IMIDAZOLECARBOXYLATE
4-Amino-5-ethylsulfonyl-2-methoxybenzoic acid CAS 71675-87-1
4-Amino-6-chlorobenzene-1,3-disulfonamide CAS 121-30-2
Recommended......
TOP