5-AMINOVALERIC ACID HYDROCHLORIDE

CAS No.：627-95-2

Important Notice

This product is a chemical product/pharmaceutical intermediate. It is not a drug, an active pharmaceutical ingredient (API), or a pharmaceutical-grade material. It has not been granted a drug approval number or a Chemical Drug Substance Approval Notice, has not passed drug-related review and approval, and is not manufactured, tested, or released in accordance with pharmaceutical GMP.
This product is intended solely for non-clinical research, process development, quality studies, further chemical processing, or chemical synthesis. It must not be used in drug-product manufacturing, clinical trials, clinical diagnosis, or administration to humans or animals, or be sold, used as an input, submitted for regulatory filing, or released as an API or pharmaceutical material.
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5-AMINOVALERIC ACID HYDROCHLORIDE Basic information

Product Name:	5-AMINOVALERIC ACID HYDROCHLORIDE
Synonyms:	DELTA-AMINO-N-VALERIC ACID HYDROCHLORIDE;H-APE(5)-OH HCL;HOMOPIPERIDINIC ACID HYDROCHLORIDE;5-AMINOVALERIC ACID HYDROCHLORIDE;5-AMINOPENTANOIC ACID HYDROCHLORIDE;5-AMINO-N-VALERIC ACID HYDROCHLORIDE;4-carboxybutylammonium chloride;5-AminopentanoicacidHCl
CAS:	627-95-2
MF:	C5H12ClNO2
MW:	153.61
EINECS:	211-021-1
Product Categories:	omega-Aminocarboxylic Acids;omega-Functional Alkanols, Carboxylic Acids, Amines & Halides
Mol File:	627-95-2.mol

5-AMINOVALERIC ACID HYDROCHLORIDE Chemical Properties

Melting point	95-97 °C(lit.)
Boiling point	131-132 °C(Press: 3 Torr)
density	1.0962 g/cm3
form	powder to crystal
color	White to Light yellow to Light orange
Sensitive	Hygroscopic
BRN	3683907
CAS DataBase Reference	627-95-2(CAS DataBase Reference)

Safety Information

Hazard Codes	Xn
Risk Statements	20/21/22-36/37/38
Safety Statements	24/25-36-26
WGK Germany	3

MSDS Information

Provider	Language
ACROS	English
SigmaAldrich	English
ALFA	English

5-AMINOVALERIC ACID HYDROCHLORIDE Usage And Synthesis

Chemical Properties	LIGHT PINK CRYSTALLINE POWDER
Uses	5-Aminovaleric Acid Hydrochloride is used in the synthesis of precursors and fragments of antibiotics XIV and in the study of the reaction of thiolactams with ethyl chloroacatate. Reagent in the preparation of hydroxymethyl dihydroisoxazole derivatives useful as antibiotics agents.
Purification Methods	Crystallise the salt from CHCl3. Otherwise dissolve it in EtOH and add 2 volumes of Et2O and chill. [Schniepp & Marvel J Am Chem Soc 57 1557 1935, Woods & Colver J Am Chem Soc 67 654 1945, Beilstein 4 III 1343, 4 IV 2636.]

5-AMINOVALERIC ACID HYDROCHLORIDE Preparation Products And Raw materials

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