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Dibenzyl L-Tartrate

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Dibenzyl L-Tartrate Basic information

Product Name:
Dibenzyl L-Tartrate
Synonyms:
  • Dibenzyl L-Tartrate
  • Di Benzyl-L-Tartarate
  • L-TARTARIC AIC DIBENZYL ESTER
  • L-TARTARIC ACID DIBENZYL ESTER
  • L-DBT
  • (+)-DIBENZYL-L-TARTRATE
  • DIBENZYL L-TARTRATE
  • L-(+)-Dibenzyl Tartrate
CAS:
622-00-4
MF:
C18H18O6
MW:
330.33
Product Categories:
  • Chiral Building Blocks
  • Esters (Chiral)
  • Synthetic Organic Chemistry
  • Asymmetric Synthesis
  • Chiral Catalysts, Ligands, and Reagents
  • EpoxidationChiral Building Blocks
  • Esters
  • Organic Building Blocks
Mol File:
622-00-4.mol
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Dibenzyl L-Tartrate Chemical Properties

Melting point:
51-54 °C
Boiling point:
427.78°C (rough estimate)
Density 
1.2036
refractive index 
-13 ° (C=1, Acetone)
pka
11.38±0.20(Predicted)
form 
powder to crystal
color 
White to Almost white
optical activity
[α]20/D +12.5±1°, c = 1.1% in acetone
BRN 
3221733
CAS DataBase Reference
622-00-4(CAS DataBase Reference)
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Safety Information

Safety Statements 
22-24/25
WGK Germany 
3
3-10
HS Code 
2918.13.5000

MSDS

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Dibenzyl L-Tartrate Usage And Synthesis

Uses

Polyesters could be prepared from succinyl chloride, adipoly chloride, and telephthaloyl chloride with dibenzyl L-tartrate, polyurethanes from hexamethylene diisocyanate, tolune 2,4-diisocyanate, and methylene-bis(4-phenyl isocyanate) with dibenzyl L-tartrate[1].

Synthesis

Dibenzyl L-tartrate was obtained by the reaction of L-tartaric acid. Dibenzyl L-tartrate was precipitated with petroleum ether and purified by repeated recrystallization using ethyl ether-petroleum ether. (mp 50-51℃/lit. 50°C) [C, 65.28%; H, 5.46%, (calcd: c, 65.45%; H, 5.45% for C18H1806].

References

[1] Noriyuki Kuramoto. “Carboxyl-containing polyesters and polyurethanes from dibenzyl L-tartrate.” Journal of Applied Polymer Science 29 3 (1984): 977–983.

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