4-Imidazolemethanol hydrochloride
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
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)
Safety Information
- Hazard Codes
- Xi
- Risk Statements
- 36/37/38
- Safety Statements
- 26-36-37/39
- WGK Germany
- 3
- F
- 3
- Hazard Note
- Irritant
- HS Code
- 29332900
MSDS
- Language:English Provider:4-Imidazolemethanol hydrochloride
- Language:English Provider:SigmaAldrich
- Language:English Provider:ACROS
- Language:English Provider:ALFA
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
4-Imidazolemethanol hydrochloride Preparation Products And Raw materials
Raw materials
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4-Imidazolemethanol hydrochloride(32673-41-9)Related Product Information
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- IMIDAZOLE HYDROCHLORIDE
- ETHYL 5-METHYL-1H-IMIDAZOLE-4-CARBOXYLATE
- (2-BUTYL-5-CHLORO-1H-IMIDAZOL-4-YL)METHANOL
- 4-METHYL-5-IMIDAZOLEMETHANOL HYDROCHLORIDE,4-METHYL-5-IMIDAZOLEMETHANOL HYDROCHLORIDE 98%,5-Methyl-4-imidazolemethanol hydrochloride
- (2-[(3,4-DICHLOROBENZYL)SULFANYL]-1-METHYL-1H-IMIDAZOL-5-YL)METHANOL
- 1-(4-CHLORO-BENZYL)-5-METHYL-IMIDAZOLE-4-CARBOXYLIC ACID
- [1-(2-([3-CHLORO-5-(TRIFLUOROMETHYL)-2-PYRIDINYL]AMINO)ETHYL)-2-SULFANYL-1H-IMIDAZOL-5-YL]METHANOL
- 3-(2,6-DICHLORO-BENZYLSULFANYL)-IMIDAZO[1,5-A]-PYRIDINE-1-CARBOXYLIC ACID
- 4-Imidazolemethanol hydrochloride
- (2-([3-CHLORO-5-(TRIFLUOROMETHYL)-2-PYRIDINYL]SULFANYL)-1-METHYL-1H-IMIDAZOL-5-YL)METHANOL
- (2-([(5-CHLORO-1,2,3-THIADIAZOL-4-YL)METHYL]SULFANYL)-1-METHYL-1H-IMIDAZOL-5-YL)METHANOL