191725-72-1

• 

• Basic information

  1. Product Name: 1H-Imidazole-1-ethanol,beta-methyl-(9CI)
  2. Synonyms: 1H-Imidazole-1-ethanol,beta-methyl-(9CI);2-(1H-imidazol-1-yl)-1-propanol(SALTDATA: FREE);2-(1H-Imidazol-1-yl)propan-1-ol;2-(1-imidazolyl)propan-1-ol;2-imidazol-1-ylpropan-1-ol
  3. CAS NO:191725-72-1
  4. Molecular Formula: C₆H₁₀N₂O
  5. Molecular Weight: 126.158
  6. EINECS: 268-652-0
  7. Product Categories: AMINETERTIARY
  8. Mol File: 191725-72-1.mol
  9. Article Data: 2

• Chemical Properties

  1. Melting Point: N/A
  2. Boiling Point: 289.9°C at 760 mmHg
  3. Flash Point: 129.1°C
  4. Appearance: /
  5. Density: 1.12g/cm³
  6. Vapor Pressure: 0.000984mmHg at 25°C
  7. Refractive Index: 1.541
  8. Storage Temp.: N/A
  9. Solubility: N/A
  10. CAS DataBase Reference: 1H-Imidazole-1-ethanol,beta-methyl-(9CI)(CAS DataBase Reference)
  11. NIST Chemistry Reference: 1H-Imidazole-1-ethanol,beta-methyl-(9CI)(191725-72-1)
  12. EPA Substance Registry System: 1H-Imidazole-1-ethanol,beta-methyl-(9CI)(191725-72-1)

• Safety Data

  1. Hazard Codes: N/A
  2. Statements: N/A
  3. Safety Statements: N/A
  4. WGK Germany:
  5. RTECS:
  6. HazardClass: N/A
  7. PackingGroup: N/A
  8. Hazardous Substances Data: 191725-72-1(Hazardous Substances Data)

• Suppliers
• Usage
• SDS
• Upstream product
• Downstream Products
• Article

191725-72-1 Suppliers

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• 2-(1H-imidazol-1-yl)-1-propanol(SALTDATA: FREE)

  Cas No: 191725-72-1

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• Antimex Chemical Limied
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• 2-(1H-imidazol-1-yl)-1-propanol

  Cas No: 191725-72-1

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• BOC Sciences
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• 1H-Imidazole-1-ethanol,beta-methyl-(9CI)

  Cas No: 191725-72-1

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• ZHEJIANG JIUZHOU CHEM CO.,LTD
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• 2-(1H-imidazol-1-yl)propan-1-ol

  Cas No: 191725-72-1

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• Debye Scientific
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191725-72-1 Usage

Chemical structure

Imidazole ring with a beta-methyl substituent and an ethanol group

Derivative

of imidazole

Usage

in pharmaceutical and chemical research

Biological activities

potential various activities

Synthesis

used as a building block in the synthesis of other compounds

Stabilizer

used in some formulations

Applications

in both the pharmaceutical and cosmetic industries, can be found in skincare and personal care products

Check Digit Verification of cas no

The CAS Registry Mumber 191725-72-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,1,7,2 and 5 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 191725-72:
(8*1)+(7*9)+(6*1)+(5*7)+(4*2)+(3*5)+(2*7)+(1*2)=151
151 % 10 = 1
So 191725-72-1 is a valid CAS Registry Number.

InChI:InChI=1/C6H10N2O/c1-6(4-9)8-3-2-7-5-8/h2-3,5-6,9H,4H2,1H3

191725-72-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name	2-imidazol-1-ylpropan-1-ol

1.2 Other means of identification

Product number	-
Other names	EINECS 268-652-0

1.3 Recommended use of the chemical and restrictions on use

Identified uses	For industry use only.
Uses advised against	no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number	-
Service hours	Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:191725-72-1 SDS

191725-72-1Upstream product

• 288-32-4 1H-imidazole 
• 75-56-9 methyloxirane 

191725-72-1Downstream Products

191725-72-1Relevant articles and documents

Highly efficient and green chemical synthesis of imidazolyl alcohols and N-imidazolyl functionalized β-amino compounds using nanocrystalline ZSM-5 catalysts

Kore, Rajkumar,Satpati, Biswarup,Srivastava, Rajendra

, p. 8 - 17 (2014/04/03)

A solvent free protocol is developed for the synthesis of imidazolyl alcohols and N-imidazolyl functionalized β-amino compounds. Imidazolyl alcohols were synthesized by the ring opening of epoxides with imidazoles and N-imidazolyl functionalized β-amino compounds were synthesized by the hydroamination reaction of imidazoles and activated olefins. These reactions were catalyzed by a variety of crystalline heterogeneous catalysts such as Al/Zr substituted nanocrystalline ZSM-5 (M-Nano-ZSM-5), conventional M-ZSM-5 (where M = Zr, Al), and Zr substituted amorphous mesoporous catalysts (Zr-SBA-15 and Zr-KIT-6). Among these catalysts, nanocrystalline Zr-Nano-ZSM-5 exhibited the highest activity and regioselectivity. Structure activity relationship is explained based on the catalytic activity, acidity measurements, reactivity of reactants (imidazoles/epoxides/methyl acrylate), competitive adsorption, nature, and type of catalysts. Zr-Nano-ZSM-5 exhibited exceptionally high catalytic activity compared to the catalysts reported in the literature for the synthesis of imidazolyl alcohols and other imidazole derivatives.

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