95352
(−)-Dibenzyl D-tartrate
≥98.0% (sum of enantiomers, HPLC)
About This Item
Recommended Products
Quality Level
Assay
≥98.0% (sum of enantiomers, HPLC)
form
powder
optical activity
[α]20/D −12.5±1°, c = 1.1% in acetone
mp
66-70 °C
functional group
ester
hydroxyl
phenyl
SMILES string
O[C@@H]([C@H](O)C(=O)OCc1ccccc1)C(=O)OCc2ccccc2
InChI
1S/C18H18O6/c19-15(17(21)23-11-13-7-3-1-4-8-13)16(20)18(22)24-12-14-9-5-2-6-10-14/h1-10,15-16,19-20H,11-12H2/t15-,16-/m0/s1
InChI key
LCKIPSGLXMCAOF-HOTGVXAUSA-N
Related Categories
Application
- 2,3-bis(8-Methoxyoctanoyl) dibenzyl tartrate (DBT) by reacting with 8-methoxyoctanoic acid in the presence of 1-ethyl-3-(3-(dimethylamino)propyl)carbodiimide (EDCI) as a coupling reagent.
- (-)-Chicoric acid (2,3-bis{[3-(3,4-dihydroxyphenyl)-1-oxoprop-2-enyl]oxy}butanedioic acid), as a potent inhibitor.
- Diesters of aziridine-2,3-dicarboxylic acid derivatives.
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
Choose from one of the most recent versions:
Certificates of Analysis (COA)
Don't see the Right Version?
If you require a particular version, you can look up a specific certificate by the Lot or Batch number.
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Customers Also Viewed
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service