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2,3-Butanediol, 1,4-bis(3,4-dimethoxyphenyl)-2,3-dimethylis a chemical compound belonging to the butanediol family, characterized by its molecular formula C22H30O4. This diol is a colorless liquid with a sweet taste, making it suitable for various applications across different industries.

335327-93-0

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335327-93-0 Usage

Uses

Used in the Chemical Industry:
2,3-Butanediol, 1,4-bis(3,4-dimethoxyphenyl)-2,3-dimethylis used as a solvent for various chemical processes due to its ability to dissolve a wide range of substances.
Used in the Fuel Industry:
As a fuel additive, 2,3-Butanediol, 1,4-bis(3,4-dimethoxyphenyl)-2,3-dimethylenhances the performance and efficiency of fuels, contributing to cleaner combustion and reduced emissions.
Used in the Polymer and Plastics Industry:
This chemical compound is utilized in the production of polymers and plastics, where its properties contribute to the development of materials with specific characteristics for various applications.
Used in the Food and Beverage Industry:
2,3-Butanediol, 1,4-bis(3,4-dimethoxyphenyl)-2,3-dimethylis used as a flavoring agent in the food and beverage industry, capitalizing on its sweet taste to enhance the flavor profiles of various products.
Used in the Pharmaceutical Industry:
With potential medical applications, 2,3-Butanediol, 1,4-bis(3,4-dimethoxyphenyl)-2,3-dimethylis employed in the production of medications for a range of conditions, leveraging its chemical properties to develop effective treatments.

Check Digit Verification of cas no

The CAS Registry Mumber 335327-93-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,5,3,2 and 7 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 335327-93:
(8*3)+(7*3)+(6*5)+(5*3)+(4*2)+(3*7)+(2*9)+(1*3)=140
140 % 10 = 0
So 335327-93-0 is a valid CAS Registry Number.

335327-93-0SDS

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 1,4-bis(3,4-dimethoxyphenyl)-2,3-dimethylbutane-2,3-diol

1.2 Other means of identification

Product number -
Other names -

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:335327-93-0 SDS

335327-93-0Upstream product

335327-93-0Relevant academic research and scientific papers

A short synthetic route to nordihydroguaiaretic acid (NDGA) and its stereoisomer using Ti-induced carbonyl-coupling reaction

Gezginci, Mikail H,Timmermann, Barbara N

, p. 6083 - 6085 (2001)

A rapid synthetic approach to natural meso-nordihydroguaiaretic acid (NDGA) and its non-meso isomer is described from (3,4-dimethoxyphenyl)acetone using as a key step the low-valent Ti-induced carbonyl-coupling reaction of the ketone. The method involves

Novel synthetic method of nordihydroguaiaretic acid (NDGA)

-

Paragraph 0018-0026, (2020/06/16)

Nordihydroguaiaretic acid has wide physiological activity and pharmacological activity. The invention discloses a novel synthetic method of nordihydroguaiaretic acid, wherein the method comprises thefollowing steps: carrying out reductive coupling reaction on veratone serving as a raw material under the action of a catalyst to obtain pinacol; reducing pinacol by trialkylsilane or triarylsilane under the catalysis of protonic acid or Lewis acid to generate 1,4-bis(3,4-dimethoxyphenyl)-2,3-dimethylbutane; and finally, under the action of haloid acid or Lewis acid, breaking ether bonds, and synthesizing nordihydroguaiaretic acid. The structure of the compound is characterized by 1H-NMR. Raw materials and reagents used in the method are easy to obtain, the reaction route is short, the reaction conditions are mild, the yield is high, the cost is low, and a simple and convenient path is opened up for industrial synthesis of nordihydroguaiaretic acid.

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