CAS 62040-55-5

4-amino-3-phenyl-L-alanine monohydrochloride

Description:

4-Amino-3-phenyl-L-alanine monohydrochloride, with the CAS number 62040-55-5, is an amino acid derivative characterized by the presence of an amino group, a phenyl group, and a carboxylic acid functional group. This compound is a hydrochloride salt, which enhances its solubility in water, making it useful in various biochemical applications. It is a chiral molecule, existing in the L-form, which is biologically relevant and often utilized in peptide synthesis and as a building block in pharmaceuticals. The phenyl group contributes to its hydrophobic characteristics, while the amino and carboxyl groups provide the necessary functional groups for interactions in biological systems. This compound may exhibit properties such as being a potential neurotransmitter or a precursor in metabolic pathways. Its stability, solubility, and reactivity can vary depending on environmental conditions such as pH and temperature, making it important to consider these factors in practical applications. Overall, 4-amino-3-phenyl-L-alanine monohydrochloride is significant in both research and therapeutic contexts.

Formula: C₉H₁₃ClN₂O₂

InChI: InChI=1/C9H12N2O2.ClH/c10-7-3-1-6(2-4-7)5-8(11)9(12)13;/h1-4,8H,5,10-11H2,(H,12,13);1H/t8-;/m0./s1

InChI key: InChIKey=ISCZSPZLBJLJGO-QRPNPIFTSA-N

SMILES: C([C@@H](C(O)=O)N)C1=CC=C(N)C=C1.Cl

Synonyms:

• 4-Amino-3-phenyl-L-alanine HCl
• 4-amino-L-phenylalanine hydrochloride
• <span class="text-smallcaps">L</span>-Phenylalanine, 4-amino-, hydrochloride (1:1)
• <span class="text-smallcaps">L</span>-Phenylalanine, 4-amino-, monohydrochloride
• H-Phe(4-NH2)-OH・HCl
• 4-Amino-3-phenyl-L-alanine monohydrochloride
• L-Phenylalanine, 4-amino-, hydrochloride (1:1)
• L-Phenylalanine, 4-amino-, monohydrochloride
• (S)-2-amino-3-(4-aminophenyl)propanoic acid hydrochloride
• H-PHE(4-NH2)-OH HCL
• H-PHE(4-NH2)-OH XHCL
• L-4-AMINOPHENYLALANINE HYDROCHLORIDE
• 4-AMINO-L-PHENYLALANINE HYDROCHLORIDE SALT
• L-3-(p-Aminophenyl)alanine
• L-(+)-p-AMinophenylalanine Hydrochloride
• H-PHE(4-NH2) XHCL
• π-Amino-L-phenylalanine hydrochloride
• H-P-AMINO-L-PHE-OH HCL
• See: A622376
• Aminophenylalanine
• L-3-(p-AMinophenyl)alanine Hydrochloride
• 4-Nitro-L-phenylalanine hydrochloride
• 4-AMino-L-phenylalanine, HCl
• 4-Amino-L-phenylalanine hydrochloride >=96.0% (calc. on dry substance, AT)
• 4-Amino-L-phenylalanine hydrochloride≥ 99% (HPLC)
• L-P-AMINOPHENYLALANINE HYDROCHLORIDE SALT
• H-P-AMINO-PHE-OH HCL
• H-L-Phe(4-NH2)-OH*HCl
• L-Phe(4-NH2)-OH·HCl
• AMinophenylalanine Hydrochloride
• p-AMino-L-phenylalanine Hydrochloride
• L-(+)-p-Aminophenylalanine
• P-AMINO-L-PHENYLALANINE, HYDROCHLORIDE

4-Amino-L-phenylalanine, HCl

CAS: 62040-55-5

Formula: C₉H₁₃ClN₂O₂

Purity: 96%

Color and Shape: Solid

Molecular weight: 216.6647

Ref: IN-DA00EARW

4-Amino-L-phenylalanine hydrochloride

CAS: 62040-55-5

Formula: C₉H₁₂N₂O₂·HCl

Molecular weight: 216.66

Ref: 7W-GM5743

p-Amino-L-phenylalanine hydrochloride

CAS: 62040-55-5

p-Amino-L-phenylalanine hydrochloride (PABA) is a type of amino acid that is used in the synthesis of melphalan hydrochloride, a drug used to treat cancer. PABA is a white crystalline powder that can be dissolved in water and formic acid. It has been shown to interact with the hydrophilic interaction chromatography column and flow rate sensor in order to improve the chromatographic separation of ammonium formate. PABA has also been found to be chiral and can be converted into its enantiomeric form by means of an organic solvent, such as acetonitrile. The impurities of PABA are mandelic acid and l-phenylalanine. These impurities are separated from PABA by means of HPLC analysis.

Formula: C₉H₁₃ClN₂O₂

Purity: Min. 95%

Color and Shape: White/Off-White Solid

Molecular weight: 216.66 g/mol

Ref: 3D-FA17768

H-Phe(4-NH2)-OH HCl

CAS: 62040-55-5

Formula: C₉H₁₃ClN₂O₂

Purity: ≥96%

Color and Shape: Solid

Molecular weight: 216.67

Ref: 10-F219802