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63870-39-3

63870-39-3 Structure

63870-39-3 Structure
IdentificationBack Directory
[Name]

(5-AMINO-1H-1,2,4-TRIAZOL-3-YL)METHANOL
[CAS]

63870-39-3
[Synonyms]

NSC513582
ZERO/004602
ZINC02415220
ASINEX-REAG BAS 03825303
(3-Amino-1H-1,2,4-triazol-5-yl)
(5-AMINO-1H-1,2,4-TRIAZOL-3-YL)METHANOL
(5-amino-2H-1,2,4-triazol-3-yl)methanol
methanol compound with 2-hydroxyacetic acid
(3-AMINO-1H-1,2,4-TRIAZOL-5-YL)METHANOL 2-HYDROXYACETIC ACID
(3-AMino-1H-1,2,4-triazol-5-yl)Methanol coMpound with 2-hydroxyacetic acid
Acetic acid, hydroxy-, compd. with 5-amino-1H-1,2,4-triazole-3-methanol (1:1)
[Molecular Formula]

C3H6N4O
[MDL Number]

MFCD02933180
[MOL File]

63870-39-3.mol
[Molecular Weight]

114.11
Chemical PropertiesBack Directory
[Melting point ]

114-115 °C(Solv: ethanol (64-17-5))
[storage temp. ]

under inert gas (nitrogen or Argon) at 2–8 °C
[EPA Substance Registry System]

Acetic acid, hydroxy-, compd. with 5-amino-1H-1,2,4-triazole-3-methanol (1:1) (63870-39-3)
Safety DataBack Directory
[Hazard Codes ]

Xi
Hazard InformationBack Directory
[Synthesis]

Glycolic acid

79-14-1

Aminoguanidine bicarbonate

2582-30-1

(5-AMINO-1H-1,2,4-TRIAZOL-3-YL)METHANOL

63870-39-3

Aminoguanidine bicarbonate (23.5 g, 172 mmol) was added in batches to a mixture of ethanoic acid (26.2 g, 345 mmol) and water (10 mL) over a period of 0.1 hours. During the addition, the reaction mixture was gently heated to maintain the internal temperature at 25 °C. Subsequently, concentrated nitric acid (1.0 mL) was added slowly and dropwise to the reaction system, and then the reaction mixture was heated to an internal temperature of 104-108 °C over 22 hours. Upon completion of the reaction, the heating was stopped and the solution was allowed to cool naturally with stirring. The slurry cooled to 10 °C was continued to be stirred for 2 h. Subsequently, it was filtered and the filter cake was washed with ethanol (EtOH). The resulting solid was dried overnight under vacuum to afford the target product (5-amino-1H-1,2,4-triazol-3-yl) methanol ethanolate (Product 88a, 29.5 g, 85% yield). Mass spectrometry analysis: calculated value (M + H)+ = 115, measured value (M + H)+ = 115.

[References]

[1] Patent: WO2012/83105, 2012, A1. Location in patent: Page/Page column 101
[2] Patent: WO2007/23381, 2007, A1. Location in patent: Page/Page column 54-55
[3] Patent: WO2004/74270, 2004, A2. Location in patent: Page 300
[4] Patent: US2005/176701, 2005, A1. Location in patent: Page/Page column 144
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