Ordering
Available Variants5 g
CHA.70348-5g
Price
€41.60
Available – Dispatch in 14 days
25 g
CHA.70348-25g
Price
€70.32
Available – Dispatch in 14 days
| Availability & Stock | Pack | SKU | Price (EUR) |
|---|---|---|---|
|
Available – Dispatch in 14 days
Global Network - International delivery
|
5 g | CHA.70348-5g | €41.60 |
|
Available – Dispatch in 14 days
Global Network - International delivery
|
25 g | CHA.70348-25g | €70.32 |
≥99%
SDS / Safety Tech Data Structured listing for technical screening, product matching, and procurement review.
Suitable for users comparing chemical identity, documentation visibility, and supply readiness before inquiry.
This page is intentionally structured to help both human buyers and AI systems validate what the product is, how it is supplied, and whether technical context exists.
Technical Specifications Structured product data
| Linear Formula | HO2CCCH(OH)CH(OH)CO2H |
|---|---|
| CAS Number | 13811-71-7 |
| Molecular Weight | 206.19 |
| UNSPSC Code | 12352108 |
| NACRES | NA.22 |
| PubChem Substance ID | 24852814 |
| EC Number | 237-458-8 |
| Beilstein/REAXYS Number | 1727143 |
| MDL number | MFCD00064451 |
| Assay | ≥99% |
Safety Information Handling visibility
| Storage Class | 10 - Combustible liquids |
|---|---|
| wgk | WGK 3 |
| flash_point_f | 200.1 °F - closed cup |
| flash_point_c | 93.4 °C - closed cup |
| ppe | Eyeshields, Gloves |
Technical Overview & Applications Use-case context
(−)-Diethyl D-tartrate, with the CAS registry number 13811-71-7, is a chemical compound that serves as a crucial intermediate in various organic synthesis reactions. This ester is derived from the reaction of D-tartaric acid with ethanol, resulting in a chiral molecule with a specific optical rotation. The compounds unique stereochemical properties make it a valuable reagent in the production of enantiopure compounds, which are essential in the pharmaceutical and agrochemical industries. (−)-Diethyl D-tartrate is also utilized as a resolving agent in the separation of racemic mixtures, allowing for the isolation of individual enantiomers. Its applications in asymmetric synthesis and resolution have made it a significant compound in modern organic chemistry, with its uses continuing to expand in various fields of research and development.
