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1-Propene-1,2-diol, also known as 3-hydroxy-1-propene or allyl glycol, is a colorless, viscous liquid with the chemical formula C3H6O2. It is an organic compound that is a derivative of propylene glycol, featuring a hydroxyl group (-OH) at both the 1st and 2nd carbon atoms. This diol is used as a solvent, a chemical intermediate, and in the synthesis of various compounds, including pharmaceuticals and polymers. It is also known for its ability to act as a reducing agent and has applications in the production of resins and coatings. Due to its reactivity, 1-propene-1,2-diol can be used in the preparation of various esters and ethers, making it a versatile building block in organic chemistry.

7333-03-1

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7333-03-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7333-03-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,3,3 and 3 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 7333-03:
(6*7)+(5*3)+(4*3)+(3*3)+(2*0)+(1*3)=81
81 % 10 = 1
So 7333-03-1 is a valid CAS Registry Number.

7333-03-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name prop-1-ene-1,2-diol

1.2 Other means of identification

Product number -
Other names 1-Propene-1,2-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:7333-03-1 SDS

7333-03-1Upstream product

7333-03-1Downstream Products

7333-03-1Relevant academic research and scientific papers

Monitoring carbonyl-amine reaction and enolization of 1-hydroxy-2- propanone (acetol) by FTIR spectroscopy

Yaylayan, Varoujan A.,Harty-Majors, Susan,Ismail, Ashraf A.

, p. 2335 - 2340 (1999)

Infrared absorption bands characteristic of the aldehydo, keto, and enediol forms of 1-hydroxy-2-propanone (acetol) were identified and used to study the effect of solvent on the absorption frequencies and the effect of temperature and acid/base catalysis on the enolization reactions. The data indicated that, in addition to water, acids and bases can catalyze the enolization of 1-hydroxy-2-propanone and that the temperature inversely effects the rate of enolization under basic conditions. However, under acidic conditions, increasing the temperature favors the enolization process. In addition, the reaction of 1-hydroxy-2-propanone with a primary and a secondary amine was also monitored by Fourier transform infrared spectroscopy. The data indicated that at room temperature the rate of amine reaction was faster than the rate of its catalysis of enolization; however, below room temperature, the rate of base-catalyzed enolization became comparable with the rate of carbonyl-amine reaction forming both Heyns and Amadori adducts.

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