(R)-(-)-AMINO-3-HYDROXYBUTANOIC ACID
- CAS NO.：7013-07-2
- Empirical Formula: C4H9NO3
- Molecular Weight: 119.12
- MDL number: MFCD02262047
- SAFETY DATA SHEET (SDS)
- Update Date: 2023-05-09 09:30:47
What is (R)-(-)-AMINO-3-HYDROXYBUTANOIC ACID?
The Uses of (R)-(-)-AMINO-3-HYDROXYBUTANOIC ACID
(R)-4-Amino-3-hydroxybutanoic Acid is an intermediate in the synthesis of Stearoyl-L-carnitine-13C3 Chloride (S686517) which is carbon-13 labeled R-Stearoyl Carnitine Chloride (S686515), which is a carnitine ester tested for its ability to inhibit protein kinase C (PKC).
Properties of (R)-(-)-AMINO-3-HYDROXYBUTANOIC ACID
| Melting point: | 216-217 °C (decomp)(Solv: water (7732-18-5); ethanol (64-17-5)) |
| Boiling point: | 374.5±32.0 °C(Predicted) |
| Density | 1.312±0.06 g/cm3(Predicted) |
| storage temp. | Keep in dark place,Inert atmosphere,Room temperature |
| solubility | PBS (pH 7.2): 10 mg/ml |
| pka | 4.04±0.10(Predicted) |
| form | Solid |
| color | White |
| CAS DataBase Reference | 7013-07-2(CAS DataBase Reference) |
Safety information for (R)-(-)-AMINO-3-HYDROXYBUTANOIC ACID
Computed Descriptors for (R)-(-)-AMINO-3-HYDROXYBUTANOIC ACID
New Products
4-AMINO-TETRAHYDRO-PYRAN-4-CARBOXYLIC ACID HCL 4-(Dimethylamino)tetrahydro-2H-pyran-4-carbonitrile 4-AMINO-TETRAHYDRO-PYRAN-4-CARBOXYLIC ACID 4-Aminotetrahydropyran-4-carbonitrile Hydrochloride (R)-3-Aminobutanenitrile Hydrochloride 5-Bromo-2-nitropyridine Nimesulide BP Aceclofenac IP/BP/EP Diclofenac Sodium IP/BP/EP/USP Mefenamic Acid IP/BP/EP/USP Ornidazole IP Diclofenac Potassium 3-Bromopyrazole (3aR,4R,5R,6aS)-hexahydro-5-Triethyl silyloxy-4-((E)-3-oxo-5-phenylpent-1- enyl)cyclopenta[b]furan-2-one. 1-Chlorocarbonyl-4-piperidinopiperidine 1-Bromo-4-phenyl-2-Butanone 4-Amino-2-fluoro-N-methylbenzamide 1,1'-Carbonyldiimidazole SODIUM AAS SOLUTION ZINC AAS SOLUTION BUFFER SOLUTION PH 10.0(BORATE) GOOCH CRUCIBLE SINTERED AQUANIL 5 BERYLLIUM AAS SOLUTIONRelated products of tetrahydrofuran
![CARNITINE HYDROCHLORIDE, L-[N-METHYL-3H]](https://img.chemicalbook.in/StructureFile/ChemBookStructure2/GIF/CB1677324.gif)
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