5349-51-9

Basic information

• Product Name: 4-TERT-AMYLCYCLOHEXANOL
• Synonyms: 4-TERT-PENTYLCYCLOHEXANOL;4-TERT-AMYLCYCLOHEXANOL;4-TERT-AMYLCYCLOHEXANOL, 98%, MIXTURE OF CIS AND TRANS;4-tert-Amylcyclohexanol, cis + trans, 99%;4-tert-Amylcyclohexanol,cis/transmixedisomers;Cyclohexanol, 4-(1,1-dimethylpropyl)-;4-tert-amylcyclohexanol, mixture of cis and trans;4-tert-pentylcyclohexanol, cis + trans
• CAS NO: 5349-51-9
• Molecular Formula: C₁₁H₂₂O
• Molecular Weight: 170.29
• EINECS: 226-311-3
• Product Categories: Alcohols;C9 to C30;Oxygen Compounds
• Mol File: 5349-51-9.mol
• Article Data: 1

Chemical Properties

• Melting Point: 24-27 °C(lit.)
• Boiling Point: 154-155 °C40 mm Hg(lit.)
• Flash Point: >230 °F
• Appearance: /
• Density: 0.903 g/mL at 25 °C(lit.)
• Vapor Pressure: 0.0198mmHg at 25°C
• Refractive Index: 1.4637 (estimate)
• CAS DataBase Reference: 4-TERT-AMYLCYCLOHEXANOL(CAS DataBase Reference)
• NIST Chemistry Reference: 4-TERT-AMYLCYCLOHEXANOL(5349-51-9)
• EPA Substance Registry System: 4-TERT-AMYLCYCLOHEXANOL(5349-51-9)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-36
• WGK Germany: 3
• Hazardous Substances Data: 5349-51-9(Hazardous Substances Data)

Usage

General Description

4-Tert-Amylcyclohexanol is a chemical compound with the molecular formula C12H24O. It is a colorless liquid with a strong, sweet odor. This chemical is commonly used as a fragrance ingredient in various personal care and household products. It is also used as a solvent and in the production of other chemicals. 4-Tert-Amylcyclohexanol is known to have antimicrobial and antifungal properties, making it a valuable ingredient in products designed to inhibit the growth of microorganisms. However, it is important to handle this chemical with care, as it can be irritating to the skin and eyes and should be used in well-ventilated areas.

InChI:InChI=1/C11H22O/c1-4-11(2,3)9-5-7-10(12)8-6-9/h9-10,12H,4-8H2,1-3H3

Upstream product

• 16587-71-6 4-tert-amylcyclohexanone 
• 80-46-6 4-t-amylphenol 
• 109-66-0 pentane 

Downstream Products

• 199584-38-8 C₁₂H₂₄O 
• 1226494-74-1 (R)-4-{6-[4-(1,1-dimethylpropyl)-cyclohexyloxy]-naphthalen-2-yl}-4-methyloxazolidin-2-one 
• 104178-35-0 4-tert-pentyl-cyclohexane-1,2-dione 
• 31720-72-6 2-Cyclohexyl-2,3-dimethylbuttersaeure 
• 6288-20-6 acrylic acid-(4-tert-pentyl-cyclohexyl ester) 
• 16587-71-6 4-tert-amylcyclohexanone 

Relevant articles and documents

ENZYMATIC "IN VITRO" REDUCTION OF KETONES. VI.(1) Reduction rates and stereochemistry of the HLAD-catalyzed reduction of 3-alkyl- and 4-alkylcyclohexanones.

Reaction rate constants for the catalytic step HLAD-NADH + ketone * HLAD-NAD+ + alcohol in the HLAD-catalyzed reduction of 3-alkyl- and 4-alkylcyclohexanones are determined from initial rate measurements in the coenzyme recycling system ketone-ethanol-NAD+-HLAD.By rate measurements at several temperatures, activation parameters were determined and isokinetic relationships tracked down.Two different isokinetic relationships show that the 3-alkylcyclohexanones pass through an other type of transition state than cyclohexanone and the 4-alkylcyclohexanones, which means that they have a different arrangement on the HLAD-NADH complex.The results are rationalized in view of the most recent principles on nucleophilic additions to carbonyl functions.The resulting model for the HLAD-catalyzed reduction adequately explains the observed rate accelerating and decelerating effects and the stereochemistry of the reduction as well.