87061-04-9 Usage
Chemical Properties
3-[(l)-Menthoxy]propane-1,2-diol is a liquid that gives a
physiological cooling sensation on the skin and mucosa. It is used to create coolness
and freshness to cosmetic and oral care preparations.
The synthesis of menthoxypropanediol starts with menthol. Subsequent etherification
with an allyl halide and dihydroxylation yields the diol.
Uses
Different sources of media describe the Uses of 87061-04-9 differently. You can refer to the following data:
1. Menthoxypropane-1,2-diol, is a Cyclohexane derivative are disclosed in a variety of tech. products, household products, or in cosmetic and pharmaceutical compounds.?The substances are well tolerated and characterized by their good biodegradability.
2. Menthoxypropanediol is used to mask odor and leave the skin feeling refreshed, it is a synthetic menthol derivative.
Flammability and Explosibility
Notclassified
Trade name
Coolact? 10 (Takasago).
Check Digit Verification of cas no
The CAS Registry Mumber 87061-04-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,0,6 and 1 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 87061-04:
(7*8)+(6*7)+(5*0)+(4*6)+(3*1)+(2*0)+(1*4)=129
129 % 10 = 9
So 87061-04-9 is a valid CAS Registry Number.
InChI:InChI=1/C13H26O3/c1-9(2)12-5-4-10(3)6-13(12)16-8-11(15)7-14/h9-15H,4-8H2,1-3H3
87061-04-9Relevant articles and documents
A 3-L-peppermint propoxycyclohexyl propane -1,2-diol synthesis method
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Paragraph 0005; 0013, (2017/02/09)
The invention relates to a synthesis method of 3-L-menthoxypropane-1,2-diol. The synthesis method comprises the steps of reacting menthol with 1,3-dihalo-glycerol acetate under a strong alkaline condition at a low temperature to generate 1-halo-2-acetoxy-
Method for producing 3-l-menthoxypropane-1,2-diol
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, (2008/06/13)
A method for safely and efficiently producing high purity 3-l-menthoxypropane-1,2-diol and intermediates to be used in the method. As shown in the following reaction formula, 3-l-menthoxypropane-1,2-diol represented by the chemical formula (IV) is produced by adding l-menthol to a 1,2-epoxy-3-halogenopropane represented by the general formula (I) (wherein X represents a halogen atom) in an organic solvent in the presence of a Lewis acid, thereby producing a 1-halogeno-3-l-menthoxypropan-2-ol represented by the general formula (II), allowing the first intermediate to react with an alkali metal salt of an aliphatic carboxylic acid having from 1 to 5 carbon atoms to produce a 1-acyloxy-2-substituted-3-l-menthoxypropane represented by the general formula (III) and then hydrolyzing the second intermediate.