Basic information Safety Supplier Related

4-Imidazolemethanol hydrochloride

Basic information Safety Supplier Related

4-Imidazolemethanol hydrochloride Basic information

Product Name:
4-Imidazolemethanol hydrochloride
Synonyms:
  • AKOS 85
  • 4-IMIDAZOLEMETHANOL HYDROCHLORIDE
  • 4-(HYDROXYMETHYL)-1H-IMIDAZOLE
  • 4-(HYDROXYMETHYL)-1H-IMIDAZOLE HYDROCHLORIDE
  • 4-(HYDROXYMETHYL)IMIDAZOLE HCL
  • 4-(HYDROXYMETHYL)IMIDAZOLE HYDROCHLORIDE
  • 4(5)-(HYDROXYMETHYL)IMIDAZOLE
  • 4(5)-HYDROXYMETHYLIMIDAZOLE HYDROCHLORIDE
CAS:
32673-41-9
MF:
C4H7ClN2O
MW:
134.56
EINECS:
251-150-0
Product Categories:
  • Building Blocks
  • Chemical Synthesis
  • Heterocyclic Building Blocks
  • Imidazoles
  • Halogenated Heterocycles ,Quinolines
  • Hydroxymethyl's
  • Imidazoles & Benzimidazoles
  • Imidazol&Benzimidazole
  • Miscellaneous Reagents
  • Imidazoles & Benzimidazoles
  • Alcohols and Derivatives
  • Heterocycles
Mol File:
32673-41-9.mol
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4-Imidazolemethanol hydrochloride Chemical Properties

Melting point:
110 °C
storage temp. 
2-8°C
solubility 
water: soluble50mg/mL, clear to slightly hazy, colorless to yellow
form 
crystalline
color 
off-white to yellow
Water Solubility 
Soluble in water.
BRN 
3562041
Stability:
Hygroscopic
CAS DataBase Reference
32673-41-9(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36-37/39
WGK Germany 
3
3
Hazard Note 
Irritant
HS Code 
29332900

MSDS

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4-Imidazolemethanol hydrochloride Usage And Synthesis

Chemical Properties

light yellow to beige or light brown crystalline

Uses

Synthesis of imidazole-containing peptidomimetic inhibitors.1

Uses

4-Imidazolemethanol hydrochloride was used in the synthesis of imidazole-containing peptidomimetic inhibitors.

Synthesis

50-00-0

96-26-4

32673-41-9

A solvent mixture of acetonitrile and ethanol with a volume ratio of 2:1 was added to the reactor, and 100 mmol of 1,3-dihydroxyacetone and 200 mmol of formaldehyde were added sequentially and stirred until complete dissolution. Subsequently, 100 mmol of ceric ammonium nitrate was added as an oxidizing agent. The pH of the reaction system was adjusted to 10 by slow dropwise addition of sodium ethanolate solution at atmospheric pressure and 60 °C, and 15 mmol of catalyst was added. The reaction was stirred under this condition for 8 hours, and 4-hydroxymethylimidazole was obtained after completion of the reaction. To the reaction solution, concentrated hydrochloric acid was added dropwise to adjust the pH to 2, and the precipitate was collected by filtration. The solid was washed with saturated sodium chloride solution and subsequently recrystallized with ethanol. Finally, the product was dried under vacuum to obtain 4-hydroxymethylimidazole hydrochloride. The purity of the product was determined to be 98.2% and the yield was 87.5%.

References

[1] Patent: CN106349165, 2017, A. Location in patent: Paragraph 0016-0030

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