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Methyl (S)-(+)-3-hydroxybutyrate, 98%, Thermo Scientific Chemicals
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Catalog number L19996.06
also known as L19996-06
Price (USD)/ Each
120.00
-
Quantity:
5 g
Price (USD)/ Each
120.00
Methyl (S)-(+)-3-hydroxybutyrate, 98%, Thermo Scientific Chemicals
Catalog numberL19996.06
Price (USD)/ Each
120.00
-
Chemical Identifiers
CAS53562-86-0
IUPAC Namemethyl 3-hydroxybutanoate
Molecular FormulaC5H10O3
InChI KeyLDLDJEAVRNAEBW-UHFFFAOYNA-N
SMILESCOC(=O)CC(C)O
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Specifications
Specification Sheet
Specification SheetRefractive Index1.4200-1.4240 @ 20?C
Appearance (Color)Clear, colorless
FormLiquid
Optical Rotation+48.5? ± 2? (c=1.3 in Chloroform)
Assay (GC)>97.5%
Methyl (S)-(+)-3-hydroxybutyrate serves as an optically active starting material used in organic synthesis. It is also used in the preparation of (-)-methyl elenolate.
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
Methyl (S)-(+)-3-hydroxybutyrate serves as an optically active starting material used in organic synthesis. It is also used in the preparation of (-)-methyl elenolate.
Solubility
Miscible with alcohol. Immiscible with water.
Notes
Incompatible with oxidizing agents, bases and acids.
Methyl (S)-(+)-3-hydroxybutyrate serves as an optically active starting material used in organic synthesis. It is also used in the preparation of (-)-methyl elenolate.
Solubility
Miscible with alcohol. Immiscible with water.
Notes
Incompatible with oxidizing agents, bases and acids.
RUO – Research Use Only
General References:
- Morikawa, T.; Ninomiya, K.; Takamori, Y.; Nishida, E.; Yasue, M.; Hayakawa, T.; Muraoka, O.; Li, X.; Nakamura, S.; Yoshikaw, M.; Matsuda, H. Oleanane-type triterpene saponins with collagen synthesis-promoting activity from the flowers of Bellis perennis. Phytochemistry 2015, 116, 203-212.
- Serra, S. Recent Advances in the Synthesis of Carotenoid-Derived flavors and Fragrances. Molecules 2015, 20 (7), 12817-12840.