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Thermo Scientific Chemicals
(S)-(+)-Mandelic acid, 99+%
CAS: 17199-29-0 | C8H8O3 | 152.149 g/mol
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Catalog number A15061.06
also known as A15061-06
Price (USD)
25.40
Each
Quantity:
5 g
Price (USD)
25.40
Each
Chemical Identifiers
CAS17199-29-0
IUPAC Name(2S)-2-hydroxy-2-phenylacetic acid
Molecular FormulaC8H8O3
InChI KeyIWYDHOAUDWTVEP-ZETCQYMHSA-N
SMILESO[C@H](C(O)=O)C1=CC=CC=C1
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Specifications
Specification Sheet
Specification SheetAppearance (Color)White
Identification (FTIR)Conforms
Melting Point (clear melt)129.0-136.0?C
Optical Rotation156.5 ± 1.0? (C=5 in water)
FormCrystals or powder or crystalline powder
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(S)-(+)-Mandelic acid is a versatile reagent used in the resolution of racemates and the preparation of amides, Pharmaceutical Intermediates.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
(S)-(+)-Mandelic acid is a versatile reagent used in the resolution of racemates and the preparation of amides, Pharmaceutical Intermediates.
Solubility
Soluble in water.
Notes
Light Sensitive. Keep container tightly closed. Store in cool, dry conditions in well sealed containers.
(S)-(+)-Mandelic acid is a versatile reagent used in the resolution of racemates and the preparation of amides, Pharmaceutical Intermediates.
Solubility
Soluble in water.
Notes
Light Sensitive. Keep container tightly closed. Store in cool, dry conditions in well sealed containers.
RUO – Research Use Only
General References:
- Kenichi Sakai.; Rumiko Sakurai.; Atsushi Yuzawa.; Yuka Kobayashi.; Kazuhiko Saigo. Resolution of 3-(methylamino)-1-(2-thienyl)propan-1-ol, a new key intermediate for duloxetine, with (S)-mandelic acid. Tetrahedron: Asymmetry. 2003, 14, (12), 1631-1636.
- Han-Rong Huang.; Jian-He Xu.; Yi Xua, Jiang Pan.; Xiang Liu. Preparation of (S)-mandelic acids by enantioselective degradation of racemates with a new isolate Pseudomonas putida ECU1009. Tetrahedron: Asymmetry. 2005, 16, (12), 2113-2117.