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33599-07-4

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33599-07-4 Usage

Chemical structure

A complex chemical compound with a unique arrangement of atoms and functional groups.

Industrial applications

Widely used in various industries, including food, pharmaceuticals, personal care products, cosmetics, and skincare.

Emulsifier and stabilizer

Acts as an emulsifier and stabilizer in the production of food, pharmaceuticals, and personal care products, helping to maintain a uniform mixture and prevent separation.

Check Digit Verification of cas no

The CAS Registry Mumber 33599-07-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,5,9 and 9 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 33599-07:
(7*3)+(6*3)+(5*5)+(4*9)+(3*9)+(2*0)+(1*7)=134
134 % 10 = 4
So 33599-07-4 is a valid CAS Registry Number.

33599-07-4SDS

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 2,3-diacetyloxypropyl octadecanoate

1.2 Other means of identification

Product number -
Other names 1,2-diacetoxy-3-stearoyloxy-propane

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:33599-07-4 SDS

33599-07-4Downstream Products

33599-07-4Relevant articles and documents

A two-acetyl glycerin monostearate preparation method (by machine translation)

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Paragraph 0021; 0022; 0023; 0024; 0025; 0026; 0027; 0028, (2018/11/03)

The present invention provides a two-acetyl glycerin monostearate preparation method, comprises the following steps: using toluene as a reaction solvent, the glycerin monostearate and acetic anhydride according to 1:2 - 4 molar ratio is added to the bottle, in the presence of acid catalysis of the 110 - 120 °C reflux reaction, side reaction side water diversion, after the reaction the solvent is removed by rotary evaporation, the resulting saturated sodium carbonate aqueous solution residue for repeated washing, then with anhydrous sodium sulfate dehydration and drying to obtain b b [...] crude glycerol stearate; the obtained crude product using silica gel column chromatography to separate and purify, and then the rotation of the pressure under the conditions of the solvent is removed by evaporation, to obtain high-purity of the b b [...] stearic acid glyceride. This method is simple in operation, safety, environmental hazard, the resulting product has high purity, can meet the quality requirements of the pharmaceutical excipients. (by machine translation)

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