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2217-14-3

Dipropyl tartrate, also known as dipropyltartaric acid or 2,3-dihydroxybutanedioic acid dipentyl ester, is a chemical compound with the molecular formula C11H20O6. It is a diester derived from tartaric acid, where the two hydroxyl groups of tartaric acid are esterified with propyl groups. Dipropyl tartrate is a white crystalline solid that is soluble in water and various organic solvents. It is commonly used as a chiral auxiliary in organic synthesis, particularly in the preparation of enantiomerically pure compounds, and as a reagent in the resolution of racemic mixtures. The compound is also employed in the pharmaceutical industry for the synthesis of various drugs and as a flavoring agent in the food industry.

2217-14-3

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2217-14-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2217-14-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,2,1 and 7 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 2217-14:
(6*2)+(5*2)+(4*1)+(3*7)+(2*1)+(1*4)=53
53 % 10 = 3
So 2217-14-3 is a valid CAS Registry Number.

2217-14-3SDS

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 dipropyl 2,3-dihydroxybutanedioate

1.2 Other means of identification

Product number -
Other names Dipropyl tartrate

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:2217-14-3 SDS

2217-14-3Relevant articles and documents

Enantioselective distribution of amino-alcohols in a liquid-liquid two-phase system containing dialkyl L-tartrate and boric acid

Abe,Shoji,Kobayashi,Qing,Asai,Nishizawa

, p. 262 - 265 (2007/10/02)

Racemic amino-alcohols such as pindolol, propranolol, alprenolol and bucumolol enantiomers exhibited different distribution behaviors in a two-phase system consisting of a chloroform solution of didodecyl L-tartrate and an aqueous solution of boric acid. It seemed that a borate complex of the 1,2-diol group of the tartrate and the amino-alcohol was formed in the system. In the case of pindolol, one enantiomer was preferentially extracted into the organic phase (x 2.20) at equilibrium.

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