87887-12-5

Basic information

• Product Name: 1-[(2,2,6-trimethylcyclohexyl)oxy]pentan-2-ol
• Synonyms: 1-[(2,2,6-trimethylcyclohexyl)oxy]pentan-2-ol;1-[(2,2,6-Trimethylcyclohexyl)oxy]-2-pentanol;Einecs 289-356-8
• CAS NO: 87887-12-5
• Molecular Formula: C14H28O2
• Molecular Weight: 228.37092
• EINECS: 289-356-8
• Mol File: 87887-12-5.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 267.1°C at 760 mmHg
• Flash Point: 82.8°C
• Appearance: /
• Density: 0.92g/cm³
• Vapor Pressure: 0.00113mmHg at 25°C
• Refractive Index: 1.463
• CAS DataBase Reference: 1-[(2,2,6-trimethylcyclohexyl)oxy]pentan-2-ol(CAS DataBase Reference)
• NIST Chemistry Reference: 1-[(2,2,6-trimethylcyclohexyl)oxy]pentan-2-ol(87887-12-5)
• EPA Substance Registry System: 1-[(2,2,6-trimethylcyclohexyl)oxy]pentan-2-ol(87887-12-5)

Safety Data

• Hazardous Substances Data: 87887-12-5(Hazardous Substances Data)

Usage

Physical state

Clear, colorless liquid

Odor

Mild, floral

Uses

a. Fragrance ingredient in personal care and household products
b. Solvent and emulsifying agent in cosmetic formulations
c. Plasticizer in the manufacturing of plastics
d. Flavoring agent in food products

Safety

Generally regarded as safe, but should be handled and used with care, following all safety guidelines and regulations.

InChI:InChI=1/C14H28O2/c1-5-7-12(15)10-16-13-11(2)8-6-9-14(13,3)4/h11-13,15H,5-10H2,1-4H3

Upstream product

• 362044-44-8 (+)-(1R,6S)-2,2,6-trimethylcyclohexanol 
• 139406-51-2 (R)-2-propylethylene oxide 
• 123731-68-0 (S)-1,2-epoxypentane 
• 31720-69-1 1,2,2-trimethylcyclohexanol 
• 1003-14-1 2-pentyloxirane 
• 10130-91-3 2,2,6-trimethyl-cyclohexanol 
• 5343-92-0 1,2-pentanediol 
• 2408-37-9 2,2,6-trimethylcyclohexan-1-one 
• 6155-96-0 (2R)-2-Chloropentanoic acid 
• 2013-12-9 D-norvaline 
• 139365-00-7 (2R)-2-chloropentan-1-ol 
• 362044-40-4 (-)-(1S,6R)-2,2,6-trimethylcyclohexanol 
• 32644-12-5 (2S)-2-chloropentanoic acid 
• 6600-40-4 L-Norvaline 

Relevant articles and documents

USE OF COMPOUNDS AS SELF-TANNING SUBSTANCES AND TANNING COMPOSITIONS THEREOF

The invention relates to the use of a compound of formula (IIb), (IIa), (IIIa), (IV), (Ie), (If), (Ig), (Ic), or (Id), a racemate, a stereoisomer, a tautomer, a salt, and/or a solvate thereof, including mixtures thereof, as self-tanning substance, wherein the dash bond ..... represents an optional double bond; and wherein R1, R2, R3, R4, R5, R6, R7, R8, R9, R10, R20, R21, R22, R23, R24, R25, R27, R28, R29, R40, R42, R43, R44, R45, R46, R47, R50, R51 are as defined in the claims. The invention also relates to a compound of formula (Ih), or a racemate, a stereoisomer, a tautomer, a salt, and/or a solvate thereof, including mixtures thereof; (Ih) wherein R5 is as defined in the claims. The invention also relates to self-tanning composition prepared using a compound as defined in the claims, as self-tanning substance. The invention also relates to the use of a compound or a composition as defined herein, for increasing the amount of melanin in melanocytes, for increasing melanin synthesis, for improving melanin transport and/or for improving the distribution of melanin in suprabasal layers, and/or for darkening skin and/or for sunless tanning.

Optically active, oxygenated, alicyclic compounds and their use as perfuming ingredients

The compounds of the formula wherein R1 and R2 represent, independently from each other, a hydrogen atom or a methyl group and R3 represents a linear or branched, saturated or unsaturated, lower alkyl radical, in the form of an optically active isomer of the formula wherein the wavy line indicates one or other of the two possible orientations of the OH group, and mixtures of these isomers can be used to impart fragrances of the woody and amber-scented type, devoid of any animal/perspiration characteristics, to consumer products.

Oxygenated alicyclic compounds

The compounds of formula wherein symbol R represents a C1 -C3 alkyl radical and X a substituted cyclohexyloxy group of formula STR1 wherein index n stands for zero or one, the dashed lines indicate a single bond (n=1) or a double bond in position 2 (n=0) or 3 (n=1) and each of symbols R1 to R6 designates a hydrogen atom or a methyl radical, are new and can be conveniently utilized as perfuming and flavoring ingredients. They develop in particular woody-ambery notes.