21129-27-1

Basic information

• Product Name: 1-methyl-4-(isopropyl)cyclohexan-1-ol
• Synonyms: Cyclohexanol, 1-methyl-4-(1-methylethyl)-; 1-Methyl-4-(1-methylethyl)cyclohexanol; 1-Methyl-4-(isopropyl)cyclohexan-1-ol; 1-methyl-4-(propan-2-yl)cyclohexanol
• CAS NO: 21129-27-1
• Molecular Formula: C₁₀H₂₀O
• Molecular Weight: 156.2652
• EINECS: 244-230-1
• Mol File: 21129-27-1.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 208.5°C at 760 mmHg
• Flash Point: 83.4°C
• Density: 0.898g/cm³
• Vapor Pressure: 0.0495mmHg at 25°C
• Refractive Index: 1.461
• CAS DataBase Reference: 1-methyl-4-(isopropyl)cyclohexan-1-ol(CAS DataBase Reference)
• NIST Chemistry Reference: 1-methyl-4-(isopropyl)cyclohexan-1-ol(21129-27-1)
• EPA Substance Registry System: 1-methyl-4-(isopropyl)cyclohexan-1-ol(21129-27-1)

Safety Data

• Hazardous Substances Data: 21129-27-1(Hazardous Substances Data)

Usage

General Description

1-methyl-4-(isopropyl)cyclohexan-1-ol is a chemical compound with the molecular formula C10H20O. It is a colorless liquid with a pleasant odor. 1-methyl-4-(isopropyl)cyclohexan-1-ol is used in the manufacturing of perfumes, as well as in the synthesis of other chemicals. It is also used as a solvent and as a flavoring agent in the food industry. 1-methyl-4-(isopropyl)cyclohexan-1-ol has been shown to have antimicrobial properties and is used in some pharmaceutical preparations. It is important to handle this compound with care, as it may cause irritation to the skin, eyes, and respiratory system.

Upstream product

• 99-82-1 Menthane 
• 91008-28-5 (1-Methyl-3-isopropyl-cyclopentyl-⁽¹⁾)-carbinol 
• 74233-53-7 1-p-menthanyl chloride 
• 7647-01-0 hydrogenchloride 
• 408330-48-3 (+/-)-C-(3-isopropyl-1-methyl-cyclopentyl)-methylamine 
• 138-87-4 beta-terpineol 
• 120749-17-9 1-methyl-4-(1-methylethenyl)-2,3-dioxabicyclo<2.2.2>oct-5-ene 
• 26252-11-9 dihydro-β-terpinyl acetate 
• 1195-31-9 (+)-p-menth-1-ene 
• 512-85-6 ascaridole 

Downstream Products

• 61585-35-1 p-menth-1-ene 

Relevant articles and documents

Selective aerobic hydroxylation of p-menthane to dihydroterpineols catalyzed by metalloporphyrins in solvent and additive free system

Metallodeuteroporphyrins (MDPs) were employed as the catalysts for aerobic hydroxylation of p-menthane in absence of solvents and additives under ambient pressure. Tertiary C-H bonds were found to be more active than secondary and primary C-H bonds. Thus,

OXYGENATED DERIVATIVES OF MENTHATRIENE IN PARSLEY LEAVES

The analysis of aroma volatiles of parsley revealed the presence of two novel oxygenated p-mentha-1,3,8-tiene derivatives, the amounts of which increase during processing of plant material and deteriorate the typical fresh aroma.The two derivatives, which could be synthesized by means of a dye sensitized photooxygenation reaction, were identified as 1-methyl-4(methylethenyl)-2,3-dioxabicyclooct-5-ene and 4-methyl-7-(methylethenyl)-3,8-dioxatricyclo2-4>octane.Key Word Index - Petroselinum crispum; Umbelliferae; parsley; aroma volatiles; p-mentha-1,3,8-triene; dioxetane; 1-methyl-4-(methylethenyl)-2,3-dioxabicyclooct-5-ene; diepoxide; 4-methyl-7-(methylethenyl)-3,8-dioxatricyclo2-4>octane.