2768-12-9

Basic information

• Product Name: 2,6-dimethylheptan-1-ol
• Synonyms: 2,6-diMethyl-1-heptanol
• CAS NO: 2768-12-9
• Molecular Formula: C₉H₂₀O
• Molecular Weight: 144.25
• Mol File: 2768-12-9.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 189.1°C at 760 mmHg
• Flash Point: 76.3°C
• Appearance: /
• Density: 0.822g/cm³
• Vapor Pressure: 0.158mmHg at 25°C
• Refractive Index: 1.428
• PKA: 15.04±0.10(Predicted)
• CAS DataBase Reference: 2,6-dimethylheptan-1-ol(CAS DataBase Reference)
• NIST Chemistry Reference: 2,6-dimethylheptan-1-ol(2768-12-9)
• EPA Substance Registry System: 2,6-dimethylheptan-1-ol(2768-12-9)

Safety Data

• Hazardous Substances Data: 2768-12-9(Hazardous Substances Data)

Usage

General Description

2,6-dimethylheptan-1-ol is a chemical compound with the molecular formula C9H20O. It is a colorless liquid with a floral, fruity odor, and is often used as a fragrance ingredient in perfumes and personal care products. 2,6-dimethylheptan-1-ol is also known for its antifungal properties and has been used in the development of antifungal medications. Additionally, 2,6-dimethylheptan-1-ol can be used as a solvent for various applications, as well as a chemical intermediate in the production of other compounds. It is important to handle this chemical with care and follow safety protocols, as it may pose health risks if not used properly.

InChI:InChI=1/C9H20O/c1-8(2)5-4-6-9(3)7-10/h8-10H,4-7H2,1-3H3

Upstream product

• 3327-66-0 2,6-dimethylheptanal 
• 106-72-9 2,6-dimethyl-5-hepten-1-al 
• 84606-47-3 ammonium 2,6-dimethylheptyl sulfate 

Relevant articles and documents

Isolation and absolute configuration determination of aliphatic sulfates as the Daphnia kairomones inducing morphological defense of a phytoplankton

2,6-Dimethylheptyl sulfate (1) and 6-methyloctyl sulfate (3) were isolated from Daphnia pulex as the Daphnia kairomones that induced morphological defense of a freshwater phytoplankton Scenedesmus gutwinskii var. heterospina (NIES-802). The absolute stere

Rapid synthesis of unsaturated alcohols under mild conditions by highly selective hydrogenation

Ir-ReOx/SiO2 acted as a highly active and selective heterogeneous catalyst for the hydrogenation of unsaturated aldehydes to unsaturated alcohols in water at low H2 pressure (0.8 MPa) and low temperature (303 K). The catalysis is derived from the synergy between Ir metal and ReOx.

ALKYL SULFATES FROM THE ASCIDIAN Holocynthia roretzi

-