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Home/Compounds/Research Reagent/L-phenylalaninol
C9H13NO
151.21 g/mol
Research ReagentDanger

PHENYLALANINOL, (S)-

CAS3182-95-4EC221-674-4
Category
Research Reagent
Compound Class
Amine
Primary Use
Research Compound

PHENYLALANINOL, (S)-, also known as L-phenylalaninol, is an amino alcohol compound derived from the reduction of the carboxy group of L-phenylalanine to an alcohol. It is a research reagent primarily used in amino alcohol studies and peptide-related investigations.

research compound for amino alcohol studiesbuilding block in peptide synthesis

Content scope: Information here supports chemical identification and industrial supply, research, and manufacturing contexts. It is not a therapeutic claim, medical advice, or drug-use instructions.

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Referencestereoisomer of

(2S)-2-amino-3-phenyl-1-propanol

CAS5267-64-1

research compound

Safety Reference

Corrosive
Corrosive
Danger
H314Causes severe skin burns and eye damage

Customs Tariff Classification

The international HS code for PHENYLALANINOL, (S)- (CAS 3182-95-4) is 2922.19.

HS code (international, 6-digit)

2922.19

EU CN code (8-digit)

2922 19 00

Classification per the EU customs inventory ECICS (2026-07 snapshot, HS 2022). National tariff lines and product form can affect the final classification.

Identifiers
IUPAC Name

(2S)-2-amino-3-phenylpropan-1-ol

InChIKey

STVVMTBJNDTZBF-VIFPVBQESA-N

SMILES

C1=CC=C(C=C1)C[C@@H](CO)N

Synonyms (32)
  • (S)-2-Benzylethanolamine
  • (S)-beta-Aminobenzenepropanol
  • (b-S)-b-Amino-benzenepropanol
  • (s)-phenylalaninol
  • 1-phenylalaninol
  • 2-Amino-3-phenyl-1-propanol #
  • H-Phenylalaninol
  • L-2-Amino-3-phenyl-1-propanol
  • L-2-Amino-3-phenylpropan-1-ol
  • L-Phe-ol
  • L-Phenylalaninol
  • L-Phenylalanoil
  • PHENYLALANINOL, (S)-
  • Phenylalaninol
  • bound form of Phenylalaninal
  • h-phe-ol
  • l-(s)-phenylalaninol
  • l-2-phenylalaninol
  • l-benzylglycinol

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