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2,2,4-trimethylhexane-1,6-diol, an organic compound with the molecular formula C8H18O2, is a diol characterized by the presence of two hydroxyl groups. It is synthesized through the reaction of 2,2,4-trimethylhexane with hydrogen peroxide. This versatile compound is widely recognized for its applications in the chemical industry, particularly in the production of polymers, resins, and various industrial and consumer products.

3089-24-5

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3089-24-5 Usage

Uses

Used in Chemical Industry:
2,2,4-trimethylhexane-1,6-diol is utilized as a monomer for the production of polymers and resins, contributing to the creation of materials with diverse properties and applications.
Used in Adhesives Production:
In the adhesives industry, 2,2,4-trimethylhexane-1,6-diol is employed as a component to enhance the bonding properties of adhesive formulations, improving their performance in various applications.
Used in Coatings Production:
2,2,4-trimethylhexane-1,6-diol serves as a crucial ingredient in the manufacturing of coatings, where it contributes to the film-forming properties and durability of the final product.
Used in Lubricants Production:
2,2,4-trimethylhexane-1,6-diol is used as a component in lubricants to improve their viscosity and performance, providing better protection and reducing friction in mechanical systems.
Used as a Plasticizer:
In the plastics industry, it is used as a plasticizer to increase the flexibility and workability of plastic materials, making them more suitable for a range of applications.
Used as a Precursor in Chemical Synthesis:
2,2,4-trimethylhexane-1,6-diol also functions as a precursor to other chemicals and materials, playing a vital role in the synthesis of various compounds for different industries.

Check Digit Verification of cas no

The CAS Registry Mumber 3089-24-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,0,8 and 9 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 3089-24:
(6*3)+(5*0)+(4*8)+(3*9)+(2*2)+(1*4)=85
85 % 10 = 5
So 3089-24-5 is a valid CAS Registry Number.
InChI:InChI=1/C9H20O2/c1-8(4-5-10)6-9(2,3)7-11/h8,10-11H,4-7H2,1-3H3

3089-24-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2,4-trimethylhexane-1,6-diol

1.2 Other means of identification

Product number -
Other names 2,2,4-trimethyl-1,6-hexanediol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:3089-24-5 SDS

3089-24-5Relevant academic research and scientific papers

Lactones 34 [1]. Application of alcohol dehydrogenase from horse liver (HLADH) in enantioselective synthesis of δ- and ε-lactones

Boratynski, Filip,Kielbowicz, Grzegorz,Wawrzenczyk, Czeslaw

experimental part, p. 30 - 36 (2010/12/18)

The ability of horse liver alcohol dehydrogenase (HLADH) to the enantioselective oxidation of primary-primary, primary-secondary and primary-tertiary aliphatic 1,5- and 1,6-diols 1a-i was studied. No enantioselectivity of the transformations of primary-primary 1,6-diols 1a-d to ε-lactones 4a-d was observed. Regioselective oxidation of primary-secondary 1,6-diols 1e,f and 1,5-diols 1h,i afforded enantiomerically enriched ε-lactones 4e,f and δ-lactones 4h,i. ε-Lactones 4e,f were formed with higher enantiomeric excesses (e.e. = 85-99%). Enzymatic oxidation of primary-tertiary 1,6-diol 1g did not give lactone product.

Method for blood coagulation on hard tissues

-

, (2008/06/13)

A method of using resorbable waxes for coagulation of blood on endogenous hard tissue, especially bone, which waxes consist of waxy polyester-oligomers of hydroxybarboxylic acids which are viscous to solid at body temperature. On the basis of their structure, these waxes are degradable by endogenous metabolic mechanism, wherein the rate of degradation can be adjusted.

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