H-PHE(4-NH2)-OH HCL

H-PHE(4-NH2)-OH HCL - Names and Identifiers

Name	4-amino-3-phenyl-L-alanine monohydrochloride
Synonyms	H-PHE(4-NH2) XHCL H-PHE(4-NH2)-OH HCL H-Phe(4-NH2)-OH·HCl H-PHE(4-NH2)-OH XHCL H-P-AMINO-PHE-OH HCL H-P-AMINO-L-PHE-OH HCL 4-Amino-3-phenyl-L-alanine HCl L-4-AMINOPHENYLALANINE HYDROCHLORIDE 4-amino-L-phenylalanine hydrochloride L-P-AMINOPHENYLALANINE HYDROCHLORIDE SALT 4-amino-3-phenyl-L-alanine monohydrochloride 4-Amino-3-phenyl-L-alanine monohydrochloride (2S)-2-amino-3-(4-aminophenyl)propanoic acid hydrochloride
CAS	62040-55-5
EINECS	263-388-2
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

H-PHE(4-NH2)-OH HCL - Physico-chemical Properties

Molecular Formula	C9H13ClN2O2
Molar Mass	216.66
Boling Point	383.5°C at 760 mmHg
Specific Rotation(α)	8.7 º (c=1% in 80% acetic acid)
Flash Point	185.8°C
Solubility	Acetic Acid, Water
Vapor Presure	1.44E-06mmHg at 25°C
Appearance	Powder
Color	Off-White
BRN	3657715
Storage Condition	Keep in dark place,Inert atmosphere,Room temperature

H-PHE(4-NH2)-OH HCL - Risk and Safety

Safety Description	S22 - Do not breathe dust. S24/25 - Avoid contact with skin and eyes.
WGK Germany	3
FLUKA BRAND F CODES	10-23

H-PHE(4-NH2)-OH HCL - Introduction

4-amino-3-phenyl-L-alanine monohydrochloride is an organic compound containing a hydrochloride salt. Its chemical formula is C9H11NO2 · HCl.

The compound is a white crystalline solid, soluble in water and some organic solvents. It has the structure of phenylalanine, in which an amino group and a carbonyl group are attached to the phenyl ring, and the carbonyl group is attached to the carboxyl group. This gives the compound properties similar to those of natural amino acids.

4-amino-3-phenyl-L-alanine monohydrochloride has a wide range of applications in the field of medicine. It is an important intermediate in the synthesis of drugs and can be used to prepare compounds with physiological activity, such as anti-tumor drugs, anti-cancer drugs, anti-viral drugs and so on.

The preparation of 4-amino-3-phenyl-L-alanine monohydrochloride can be carried out by a chemical synthesis method or an enzymatic catalytic method of amino acids. In general, phenylalanine is first reacted with hydrochloric acid to give the product in the form of the hydrochloride salt.

When using and storing 4-amino-3-phenyl-L-alanine monohydrochloride, care should be taken to follow relevant laboratory safety procedures. The compound may be irritating to the eyes, skin and respiratory tract. Avoid inhaling dust or contact with skin. Wear appropriate protective gloves, glasses, and a protective face mask when handling this compound. If inhaled or exposed to this substance, get medical attention immediately.

Last Update：2024-04-09 18:58:34

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