(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
Tert-butyl bis(2-chloroethyl)carbamate (S)-3-Aminobutanenitrile hydrochloride N-Boc-D-alaninol N-BOC-D/L-ALANINOL N-octanoyl benzotriazole 3,4-Dibenzyloxybenzaldehyde 4-Hydrazinobenzoic acid 1,1’-CARBONYLDIIMIDAZOLE R-2-BENZYLOXY PROPIONIC ACID 4-HYDROXY BENZYL ALCOHOL 1,1’-CARBONYLDI (1,2-4 TRIAZOLE) 3-NITRO-2-METHYL ANILINE (2-Hydroxyphenyl)acetonitrile 4-Bromopyrazole 5-BROMO-2CYANO PYRIDINE 5,6-Dimethoxyindanone 5-broMo-2-chloro-N-cyclopentylpyriMidin-4-aMine 2-(Cyanocyclohexyl)acetic acid 4-methoxy-3,5-dinitropyridine 2-aminopropyl benzoate hydrochloride 1-(4-(aminomethyl)benzyl)urea hydrochloride tert-butyl 4- (ureidomethyl)benzylcarbamate diethyl 2-(2-((tertbutoxycarbonyl)amino) ethyl)malonate Ethyl-2-chloro((4-methoxyphenyl)hydrazono)acetateRelated products of tetrahydrofuran
![CARNITINE HYDROCHLORIDE, L-[N-METHYL-3H]](https://img.chemicalbook.in/StructureFile/ChemBookStructure2/GIF/CB1677324.gif)
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