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Hexane-2,3-diol, also known as 2,3-hexanediol or methyl pentane-2,4-diol, is a colorless, viscous liquid with a molecular formula of C6H14O2 and a molecular weight of 118.18 g/mol. It is an organic compound belonging to the class of diols, characterized by the presence of two hydroxyl (-OH) groups. Hexane-2,3-diol is primarily used as a solvent, a chemical intermediate in the synthesis of various chemicals, and as a component in the production of polymers and resins. It is also employed in the manufacturing of paints, varnishes, and adhesives. Due to its low toxicity and high solubility, hexane-2,3-diol is considered a safer alternative to other solvents in certain applications.

617-30-1

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617-30-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 617-30-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,1 and 7 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 617-30:
(5*6)+(4*1)+(3*7)+(2*3)+(1*0)=61
61 % 10 = 1
So 617-30-1 is a valid CAS Registry Number.

617-30-1SDS

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 hexane-2,3-diol

1.2 Other means of identification

Product number -
Other names 2,3-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:617-30-1 SDS

617-30-1Relevant academic research and scientific papers

Chromium-Catalyzed Production of Diols From Olefins

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Paragraph 0111, (2021/03/19)

Processes for converting an olefin reactant into a diol compound are disclosed, and these processes include the steps of contacting the olefin reactant and a supported chromium catalyst comprising chromium in a hexavalent oxidation state to reduce at least a portion of the supported chromium catalyst to form a reduced chromium catalyst, and hydrolyzing the reduced chromium catalyst to form a reaction product comprising the diol compound. While being contacted, the olefin reactant and the supported chromium catalyst can be irradiated with a light beam at a wavelength in the UV-visible spectrum. Optionally, these processes can further comprise a step of calcining at least a portion of the reduced chromium catalyst to regenerate the supported chromium catalyst.

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