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2,5-Dimethyl-1,5-hexadiene-3,4-diol, commonly known as neopentyl glycol, is a chemical compound characterized by the molecular formula C5H12O2. It is a clear, colorless liquid with a slightly sweet odor. Neopentyl glycol is recognized for its versatility in the chemical industry, serving as a key component in the synthesis of various polymers and as a crosslinking agent in polyurethane production.

4723-10-8

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4723-10-8 Usage

Uses

Used in the Production of Polyester Resins:
Neopentyl glycol is utilized as a raw material in the production of polyester resins, contributing to their formation and enhancing their properties. It plays a crucial role in the polymerization process, leading to the creation of durable and high-quality resins.
Used in the Production of Coatings:
In the coatings industry, neopentyl glycol is employed as a component in the formulation of various types of coatings. Its inclusion improves the performance characteristics of the coatings, such as adhesion, flexibility, and resistance to environmental factors.
Used in the Production of Adhesives:
Neopentyl glycol is used as a component in adhesive formulations, where it contributes to the adhesive's bonding strength and durability. Its presence in adhesives helps to create strong, long-lasting bonds between different materials.
Used as a Plasticizer:
Neopentyl glycol serves as a plasticizer, enhancing the flexibility and workability of various plastics. It is incorporated into plastic materials to improve their malleability and reduce brittleness, making them more suitable for a wide range of applications.
Used in the Synthesis of Polymers:
As a building block, neopentyl glycol is used in the synthesis of various polymers. Its chemical structure allows it to react with other monomers, leading to the formation of new polymers with unique properties and applications.
Used as a Crosslinking Agent in Polyurethane Production:
Neopentyl glycol is employed as a crosslinking agent in the production of polyurethane. It helps to create a network of chemical bonds between polyurethane molecules, resulting in improved mechanical properties and durability of the final product.
Environmental and Safety Considerations:
Neopentyl glycol is considered to be relatively non-toxic and non-irritating, making it a safer choice for use in various industrial applications. Additionally, it is not known to have any significant environmental impact, which is an important factor in today's environmentally conscious world.

Check Digit Verification of cas no

The CAS Registry Mumber 4723-10-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,7,2 and 3 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 4723-10:
(6*4)+(5*7)+(4*2)+(3*3)+(2*1)+(1*0)=78
78 % 10 = 8
So 4723-10-8 is a valid CAS Registry Number.
InChI:InChI=1/C8H14O2/c1-5(2)7(9)8(10)6(3)4/h7-10H,1,3H2,2,4H3

4723-10-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,5-dimethylhexa-1,5-diene-3,4-diol

1.2 Other means of identification

Product number -
Other names 2,5-dimethyl-hexa-1,5-diene-3,4-diol

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:4723-10-8 SDS

4723-10-8Relevant academic research and scientific papers

REGIO-CONTROLLED FUNCTIONALIZATION OF 2,5-DIMETHYL-2,4-HEXADIENE INTO EPOXY ALCOHOLS BY PHOTOOXYGENATION IN THE PRESENCE OF TITANIUM(IV) OR VANADIUM(V)

Adam, Waldemar,Staab, Eugen

, p. 531 - 534 (2007/10/02)

Using Ti(OiPr)4 as oxygen transfer catalyst, the diene 1 afforded exclusively the epoxy alcohol 1c, but VO(acac)2 gave exclusively the isomerized epoxy alcohol 2c during its ene reaction with singlet oxygen.

A HIGHLY STEREOSELECTIVE PINACOLIZATION OF AROMATIC AND α,β-UNSATURATED ALDEHYDES MEDIATED BY TITANIUM(III)-MAGNESIUM(II) COMPLEX

Handa, Yuichi,Inanaga, Junji

, p. 5717 - 5718 (2007/10/02)

Reduction of Cp2TiCl2 with sec-BuMgCl in THF gave a greenish deep brown solution which has been found to promote the reductive homocoupling of aromatic and α,β-unsaturated aldehydes to yield symmetrical 1,2-diols with high threo-selectivity.

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