(+)-Diethyl L-tartrate , 99% , 87-91-2

Synonym(s):
(+)-Diethyl L-tartrate;L-(+)-Tartaric acid diethyl ester

CAS NO.：87-91-2

Empirical Formula: C8H14O6

Molecular Weight: 206.19

MDL number: MFCD00009143

EINECS: 201-783-3

PRODUCT Properties

• Melting point: 17 °C
• Boiling point: 280 °C (lit.)
• alpha: 7.5 º (neat)
• Density: 1.204 g/mL at 25 °C (lit.)
• vapor pressure: 0.402Pa at 25℃
• FEMA: 2378 | DIETHYL TARTRATE
• refractive index: n20/D 1.446(lit.)
• Flash point: 200 °F
• storage temp.: Sealed in dry,Room Temperature
• solubility: Chloroform (Slightly), Water (Slightly)
• pka: 11.61±0.20(Predicted)
• form: Viscous Liquid
• color: Clear
• Odor: at 100.00 %. mild fruity wine caramellic
• Odor Type: fruity
• biological source: synthetic
• optical activity: [α]20/D +8.5°, neat
• Water Solubility: insoluble
• Merck: 14,3855
• JECFA Number: 622
• BRN: 1727145
• Dielectric constant: 4.5（20℃）
• InChIKey: YSAVZVORKRDODB-PHDIDXHHSA-N
• LogP: 0.2 at 25℃
• CAS DataBase Reference: 87-91-2(CAS DataBase Reference)
• NIST Chemistry Reference: Diethyl tartrate(87-91-2)
• EPA Substance Registry System: Butanedioic acid, 2,3-dihydroxy- (2R,3R)-, 1,4-diethyl ester (87-91-2)

Description and Uses

(+)-Diethyl L-tartrate is used as a chiral auxiliary in the Sharpless enantioselective epoxidation of allylic alcohols, for Sharpless-type enantioselective oxidation of sulfides to sulfoxides and as a chiral auxiliary in the enantioselective construction of cyclopropanes from allylic alcohols by an asymmetric Simmons-Smith reaction. It is also used as a chiral reagent in a host of chemical reactions, such as the synthesis of isoquinoline alkaloids and arundic acid, which has been used in acute ischemic stroke therapy.

Safety

• Symbol(GHS): GHS07
• Signal word: Warning
• Hazard statements: H227
• Precautionary statements: P210e-P280a-P370+P378a-P403+P235-P501a
• Hazard Codes: Xi
• Risk Statements: 36/37/38
• Safety Statements: 24/25-36-26
• WGK Germany: 3
• TSCA: Yes
• HS Code: 29181300