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2-Hydroxymenthol, also known as 2-menthol-1,8-diol, is a naturally occurring monoterpene alcohol derived from the peppermint plant (Mentha piperita). It is a colorless, viscous liquid with a strong, cooling, and minty odor. This chemical is widely used in the pharmaceutical, food, and fragrance industries due to its analgesic, anti-inflammatory, and cooling properties. 2-Hydroxymenthol is commonly found in topical analgesic creams, cough suppressants, and oral care products, as well as in various personal care and cosmetic formulations. Its清凉效果 and pleasant scent make it a popular ingredient in many consumer products.

3804-01-1

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3804-01-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3804-01-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,8,0 and 4 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 3804-01:
(6*3)+(5*8)+(4*0)+(3*4)+(2*0)+(1*1)=71
71 % 10 = 1
So 3804-01-1 is a valid CAS Registry Number.
InChI:InChI=1/C10H20O2/c1-6(2)8-5-4-7(3)9(11)10(8)12/h6-12H,4-5H2,1-3H3

3804-01-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-methyl-6-propan-2-ylcyclohexane-1,2-diol

1.2 Other means of identification

Product number -
Other names 3trans-Isopropyl-2trans-hydroxy-6trans-methyl-cyclohexanol

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:3804-01-1 SDS

3804-01-1Relevant articles and documents

Hydrogenation and conformational analysis of (1R,2R,6S)-3-methyl-6-(1- methylethenyl)cyclohex-3-ene-1,2-diol

Ardashov,Genaev,Il'ina,Korchagina,Volcho,Salakhutdinov

experimental part, p. 1786 - 1789 (2011/04/17)

Hydrogenation of (1R,2R,6S)-3-methyl-6-(1-methylethenyl)cyclohex-3-ene-1,2- diol was studied. Nickel chloride-sodium tetrahydridoborate system turned out to selectively reduce the double bond in the isopropenyl group. The results of conformational analysis of (1R,2R,6S)-3-methyl-6-(1-methylethenyl)cyclohex-3- ene-1,2-diol and its partly and completely hydrogenated derivatives were in a good agreement with the NMR data. Pleiades Publishing, Ltd., 2010.

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