87061-04-9 Usage
Uses
Used in Cosmetics and Personal Care Products:
3-[[5-Methyl-2-(1-methylethyl)cyclohexyl]oxy]propane-1,2-diol is used as a refreshing agent and odor masking agent in cosmetics and personal care products. Its cooling and refreshing sensation on the skin makes it an ideal ingredient for products such as lotions, creams, and body washes.
Used in Household Products:
In household products, 3-[[5-Methyl-2-(1-methylethyl)cyclohexyl]oxy]propane-1,2-diol is used as a fragrance ingredient and odor masking agent. Its ability to mask unpleasant odors and provide a refreshing scent makes it suitable for use in products such as air fresheners, cleaning supplies, and laundry detergents.
Used in Pharmaceutical Compounds:
3-[[5-Methyl-2-(1-methylethyl)cyclohexyl]oxy]propane-1,2-diol is used as a pharmaceutical excipient in various formulations. Its refreshing and cooling properties make it useful in topical applications such as creams, ointments, and gels for pain relief and skin irritation.
Used in Technical Products:
In technical products, 3-[[5-Methyl-2-(1-methylethyl)cyclohexyl]oxy]propane-1,2-diol is used as a solvent, emulsifier, or dispersing agent. Its ability to dissolve and stabilize various compounds makes it useful in applications such as coatings, adhesives, and sealants.
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
-
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
-
, (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.
Process for producing 3-1-menthoxypropane-1,2-diol
-
Page column 15, (2008/06/13)
A process for producing highly pure 3-1-menthoxypropane-1,2-diol safely and efficiently, and an intermediate to be used in the process. 3-1-menthoxypropane-1,2-diol represented by the chemical formula (IV) is produced by adding 1-menthol to a 1,2-epoxy-3-
3-Levo-Menthoxypropane-1,2-diol
-
, (2008/06/13)
3-l-Menthoxypropane-1,2-diol having the formula: STR1
