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5-Methyl-3-hexanol, also known as isoamyl alcohol, is a colorless liquid with a strong, fruity odor. It is a primary alcohol characterized by the chemical formula C7H16O. This versatile compound is recognized for its applications as a solvent, flavoring agent, and in the synthesis of various chemicals, as well as for its antimicrobial properties.

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  • 623-55-2 Structure
  • Basic information

    1. Product Name: 5-METHYL-3-HEXANOL
    2. Synonyms: 2-METHYL-4-HEXANOL;5-METHYL-3-HEXANOL;ETHYLISOBUTYLCARBINOL;(±)-5-methyl-hexan-3-ol;5-methylhexan-3-ol
    3. CAS NO:623-55-2
    4. Molecular Formula: C7H16O
    5. Molecular Weight: 116.2
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 623-55-2.mol
  • Chemical Properties

    1. Melting Point: -30.45°C (estimate)
    2. Boiling Point: 147°C
    3. Flash Point: 51.6°C
    4. Appearance: /
    5. Density: 0.8290
    6. Vapor Pressure: 1.28mmHg at 25°C
    7. Refractive Index: 1.4170
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 5-METHYL-3-HEXANOL(CAS DataBase Reference)
    11. NIST Chemistry Reference: 5-METHYL-3-HEXANOL(623-55-2)
    12. EPA Substance Registry System: 5-METHYL-3-HEXANOL(623-55-2)
  • 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: 623-55-2(Hazardous Substances Data)

623-55-2 Usage

Uses

Used in Food and Beverage Industry:
5-Methyl-3-hexanol is used as a flavoring agent for its distinctive fruity aroma, enhancing the taste and appeal of various food and beverage products.
Used in Perfume and Cosmetic Industry:
5-Methyl-3-hexanol serves as a solvent and fragrance component in perfumes and cosmetics, contributing to their scent profiles and improving the longevity of the fragrances.
Used in Chemical Synthesis:
5-METHYL-3-HEXANOL is utilized as a solvent in the synthesis of other chemicals, playing a crucial role in various chemical reactions and processes.
Used in Antimicrobial Applications:
Leveraging its antimicrobial properties, 5-Methyl-3-hexanol is used as an antiseptic, helping to prevent infection and maintain cleanliness in various settings.
Used in Manufacturing Processes:
5-Methyl-3-hexanol is employed in the manufacturing of perfumes and cosmetics, where it acts as a solvent and contributes to the formulation of the final products.
Safety Note:
Due to its flammable nature, 5-Methyl-3-hexanol should be handled with care to prevent accidents and ensure safe usage in all applications.

Check Digit Verification of cas no

The CAS Registry Mumber 623-55-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,2 and 3 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 623-55:
(5*6)+(4*2)+(3*3)+(2*5)+(1*5)=62
62 % 10 = 2
So 623-55-2 is a valid CAS Registry Number.
InChI:InChI=1/C7H16O/c1-4-7(8)5-6(2)3/h6-8H,4-5H2,1-3H3

623-55-2SDS

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 5-METHYL-3-HEXANOL

1.2 Other means of identification

Product number -
Other names Aethyl-isobutyl-carbinol

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:623-55-2 SDS

623-55-2Relevant articles and documents

Facile deoxygenation of dicarbonyl compounds using a samarium diiodide-additive system

Kamochi, Yasuko,Kudo, Tadahiro,Masuda, Toshinobu,Takadate, Akira

, p. 1017 - 1020 (2007/10/03)

The reduction of α- and β-dicarbonyl compounds was investigated with samarium diiodide in the presence of additive. Diketones and ketocarboxylic acids were easily reduced at room temperature to give the mono-alcohols in good to excellent yield, and ketoester afforded the saturated ester as the major product in moderate yield. These reductions containing the reductive deoxygenation can be rapidly performed under the facile and mild conditions by this method.

Cp2TiCl2-CATALYZED GRIGNARD REACTIONS. 3. REACTIONS WITH ESTERS: EFFICIENT METHODOLOGY FOR THE SYNTHESIS OF SECONDARY ALCOHOLS AND FOR THE REDUCTION OF ESTERS TO PRIMARY ALCOHOLS

Sato, Fumie,Jinbo, Takamasa,Sato, Masao

, p. 2175 - 2178 (2007/10/02)

Cp2TiCl2-catalyzed Grignard reactions with esters provide general methodology for preparation of secondary alcohols or for reduction of esters to the corresponding primary alcohols.

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