CAS 7682-20-4
:(S)-2-Aminobutyramide hydrochloride
Description:
(S)-2-Aminobutyramide hydrochloride is a chiral amine compound characterized by its amine and amide functional groups. It is the hydrochloride salt of (S)-2-aminobutyramide, which is an important building block in organic synthesis and pharmaceutical applications. The compound typically appears as a white to off-white crystalline solid, and it is soluble in water due to the presence of the hydrochloride group, which enhances its solubility. Its molecular structure includes a four-carbon backbone with an amino group (-NH2) and an amide group (-C(=O)NH2), contributing to its reactivity and potential for forming various derivatives. The chirality of the molecule is significant in biological systems, as it can influence the pharmacological properties and interactions with biological targets. (S)-2-Aminobutyramide hydrochloride is often used in research and development, particularly in the synthesis of peptides and other biologically active compounds. Proper handling and storage conditions are essential to maintain its stability and efficacy.
Formula:C4H11ClN2O
InChI:InChI=1/C4H10N2O.ClH/c1-2-3(5)4(6)7;/h3H,2,5H2,1H3,(H2,6,7);1H
InChI key:InChIKey=HDBMIDJFXOYCGK-DFWYDOINSA-N
SMILES:[C@@H](C(N)=O)(CC)N.Cl
Synonyms:- (2S)-2-Aminobutanamide hydrochloride
- (2S)-2-aminobutanamide hydrochloride (1:1)
- (L)-2-Aminobutyramide hydrochloride
- (S)-2-Aminobutyramide HCL
- (S)-2-Aminobutyramide hydrochloride
- (S)-2-aminobutanamide hydrochloride
- 2-Aminobutanamide Hydrochloride (1:1)
- Abah
- Butanamide, 2-amino-, hydrochloride (1:1), (2S)-
- Butanamide, 2-amino-, monohydrochloride, (2S)-
- Butanamide, 2-amino-, monohydrochloride, (S)-
- Butyramide, 2-amino-, monohydrochloride, <span class="text-smallcaps">L</span>-
- H-Abu-NH2・HCl
- L-2-Amino Butanamide hydrochloride
- Levetiracetam's intermediate
- S(+)-2-amino butyramide HCl
- Butyramide, 2-amino-, monohydrochloride, L-
- Aminobutyramide Hydrochloride
- AMINOBUTYRIC ACID-NH2 HCL
- S(+)AminoButyramideHcl
- L-ALPHA-AMINOBUTYRIC ACID AMIDE HYDROCHLORIDE
- L-2-AMINO-BUTANOIC ACID HYDROCHLORIDE
- L-2-Amino
- Abu-Nh2 HCl
- (S)-2-sminobutanamide hydrochloride
- (S)-2-Aminobutanamide Monohydrochlorid
- l-2-aminobutanamide hydrochloride
- ALPHA-AMINOBUTYRIC ACID ALPHA-AMIDE HYDROCHLORIDE
- 2-AMINOBUTYRIC ACID AMIDE HYDROCHLORIDE
- (s)-2-amino-butylactamide
- H-ALPHA-ABU-NH2 HCL
- H-ABU(2)-NH2 HCL
- L-2-AMINOBUTANAMIDE HCL
- H-ABU(ALPHA)-NH2 HCL
- See more synonyms
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Found 14 products.
(S)-2-Aminobutyramide Hydrochloride
CAS:Formula:C4H10N2O·HClPurity:>98.0%(HPLC)(N)Color and Shape:White to Almost white powder to crystalMolecular weight:138.60Levetiracetam Related Compound B ((S)-2-aminobutanamide hydrochloride)
CAS:Acyclic amides (including acyclic carbamates) and their derivatives and salts thereof, nesoiFormula:C4H10N2O·HClColor and Shape:White Cream PowderMolecular weight:102.07931L-2-Aminobutanamide, HCl
CAS:Formula:C4H11ClN2OPurity:98%Color and Shape:SolidMolecular weight:138.5959Levetiracetam EP Impurity G HCl (Levetiracetam USP Related Compound B)
CAS:Formula:C4H10N2O·HClColor and Shape:White To Off-White SolidMolecular weight:102.14 36.46(S)-(+)-2-Aminobutanamide hydrochloride
CAS:(S)-(+)-2-Aminobutanamide hydrochloridePurity:98%Color and Shape:SolidMolecular weight:138.60g/mol(S)-2-Aminobutyramide hydrochloride
CAS:Formula:C4H10N2OHClColor and Shape:White to off-white or tan crystalline powderMolecular weight:138.60(S)-2-Aminobutyramide Hydrochloride
CAS:Controlled Product<p>Impurity Levetiracetam USP Related Compound B<br>Applications Levetiracetam USP Related Compound B<br></p>Formula:C4H10N2O·ClHColor and Shape:White To Off-WhiteMolecular weight:138.60(S)-2-Aminobutyramide hydrochloride
CAS:Formula:C4H11ClN2OPurity:97%Color and Shape:SolidMolecular weight:138.6(S)-2-Aminobutyramide hydrochloride
CAS:(S)-2-Aminobutyramide hydrochloride is a chiral amide compound, which is utilized primarily in scientific research settings. This compound is typically synthesized through the resolution of racemic mixtures or other specialized chemical processes that ensure the purity and stereospecificity required for research purposes.The mode of action of (S)-2-Aminobutyramide hydrochloride revolves around its role as an intermediate in chemical synthesis, serving as a building block for the production of more complex molecules. It has a noteworthy chiral configuration, which makes it an essential component in the formation of enantiomerically pure substances. This aspect is crucial in fields like pharmaceuticals, where stereochemistry can significantly impact biological activity.Its applications extend to various domains such as the synthesis of therapeutic agents, biochemical research, and the development of novel materials. Researchers value it for its ability to contribute to the fine-tuning of molecular assemblies, making it indispensable in studies focused on the interaction and function of chiral molecules. The hydrochloride form aids in its stability and solubility, which are important attributes for laboratory manipulation and experimentation.Formula:C4H10N2O•HClPurity:Min. 95%Color and Shape:White PowderMolecular weight:138.6 g/molH-Abu-NH2 HCl
CAS:H-Abu-NH2 HCl is a useful organic compound for research related to life sciences. The catalog number is T66187 and the CAS number is 7682-20-4.Formula:C4H11ClN2OColor and Shape:SolidMolecular weight:138.6














