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57456-96-9

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57456-96-9 Usage

General Description

The chemical (1R,2S,6S)-4,4,6-trimethyl-7-oxabicyclo[4.1.0]heptan-2-ol, also known as α-terpineol, is a naturally occurring monoterpene alcohol found in essential oils of various plants, including pine, cypress, and eucalyptus. It is commonly used as a fragrance and flavoring agent in the cosmetic, food, and pharmaceutical industries. α-Terpineol has a pleasant floral and lilac scent and is often added to perfumes, soaps, and lotions. It also exhibits antimicrobial, anti-inflammatory, and sedative properties, making it a popular ingredient in aromatherapy and traditional medicine. Additionally, it has been studied for its potential use as a biopesticide and repellent against insects.

Check Digit Verification of cas no

The CAS Registry Mumber 57456-96-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,4,5 and 6 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 57456-96:
(7*5)+(6*7)+(5*4)+(4*5)+(3*6)+(2*9)+(1*6)=159
159 % 10 = 9
So 57456-96-9 is a valid CAS Registry Number.

57456-96-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (1R,2S,6S)-4,4,6-trimethyl-7-oxabicyclo[4.1.0]heptan-2-ol

1.2 Other means of identification

Product number -
Other names cis-1,2-epoxy-1,5,5-trimethylcyclohexan-3-ol

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:57456-96-9 SDS

57456-96-9Upstream product

57456-96-9Relevant articles and documents

Epoxidation of allylic alcohols in aqueous solutions of non surfactant amphiphilic sugars

Denis,Misbahi,Kerbal,Ferrieres,Plusquellec

, p. 2460 - 2461 (2007/10/03)

A variety of cyclic and acyclic allylic alcohols undergo efficient chemo-, regio- and/or stereoselective epoxidations in neutral aqueous solutions of amphiphilic carbohydrates (sucrose, L-arabinose, methyl or ethyl β-D-fructopyranoside) by using dilute hydrogen peroxide in the presence of molybdic or tungstic salts.

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