70444-25-6 Usage
Physical appearance
Colorless, slightly viscous liquid 2,5-Heptanediol is a colorless liquid with a slight viscosity, making it thicker than water but still flowable.
Odor
Mild, pleasant The compound has a gentle and agreeable smell, making it suitable for use in various consumer products.
Uses
Solvent, humectant, chemical intermediate 2,5-Heptanediol is commonly used as a solvent to dissolve other substances, a humectant to retain moisture in products, and as a chemical intermediate in the synthesis of other organic compounds.
Industries
Cosmetics, personal care products, pharmaceuticals The compound is widely used in different industries, including the formulation of cosmetics, personal care items like skincare and haircare products, and pharmaceuticals.
Functional properties
Emulsifier, wetting agent, stabilizer 2,5-Heptanediol serves as an emulsifier to mix oil and water, a wetting agent to help substances disperse evenly, and a stabilizer to maintain the consistency and uniformity of various formulations.
Benefits
Improves stability and texture of emulsions The compound is known for enhancing the stability and texture of emulsions, making it an essential ingredient in skincare and haircare products.
Safety
Low toxicity, generally considered safe for use 2,5-Heptanediol is deemed to be safe for use in products due to its low toxicity level.
Check Digit Verification of cas no
The CAS Registry Mumber 70444-25-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,4,4 and 4 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 70444-25:
(7*7)+(6*0)+(5*4)+(4*4)+(3*4)+(2*2)+(1*5)=106
106 % 10 = 6
So 70444-25-6 is a valid CAS Registry Number.
InChI:InChI=1/C7H16O2/c1-3-7(9)5-4-6(2)8/h6-9H,3-5H2,1-2H3
70444-25-6Relevant articles and documents
Intramolecular H-Transfer Reactions During the Decomposition of Alkylhydroperoxides in Hydrocarbons as the Solvents
Jinsheng, Li,Pritzkow, Wilhelm,Voerckel, Volkmar
, p. 43 - 52 (2007/10/02)
Eight defined primary and secondary alkylhydroperoxides were decomposed in n-alkanes as the solvent, mostly in the presence of manganese stearate.In all cases the corresponding alcohols and carbonyl compounds were formed as the main products with yields of 60-90percent.Besides, difunctional products were formed by an intramolecular H-transfer in the alkoxy radicals corresponding to the starting hydroperoxides.Products possibly formed by an intramolecular H-transfer in the corresponding alkylperoxy radical could be found only in the case of 4-methyl-2-hydroperoxy pentane.The amount of products formed by intramolecular H-transfer depended on the nature of the C-H bond in δ-position to the original hydroperoxy group and lay between 4percent (primary C-H in the case of 4-hydroperoxy heptane) and 13percent (tertiary C-H in the case of 2-hydroperoxy-5-methyl hexane) with respect to the starting hydroperoxide.The amount of products formed by oxidative attack of the alkoxy and alkylperoxy radicals at the normal paraffins used as the solvents was unexpectedly low (always less than 10percent with respect to the starting hydroperoxide).An increment system is proposed for the calculation of 13C-nmr shifts in alkyl hydroperoxides.
