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Home/Compounds/Pharmaceutical Intermediate/(+)-2-amino-1-butanol
C4H11NO
89.14 g/mol
Pharmaceutical IntermediateDanger

(S)-(+)-2-Amino-1-butanol

CAS5856-62-2EC227-475-9
Category
Pharmaceutical Intermediate
Compound Class
Alcohol
Primary Use
Pharmaceutical Intermediate

This compound is a chiral amino alcohol used primarily as a building block in pharmaceutical manufacturing. It serves as a pharmaceutical intermediate for the synthesis of peptides and other active compounds.

pharmaceutical intermediate for 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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Related Compounds

ReferenceSame Category

2,2-Dimethylbutyryl chloride

CAS5856-77-9

pharmaceutical intermediate

ReferenceSame Category

Ethyl 2,6-dichloronicotinate

CAS58584-86-4

pharmaceutical intermediate

ReferenceSame Category

L-beta-Homoalanine hydrochloride

CAS58610-41-6

pharmaceutical intermediate

ReferenceSame Category

Tert-Butyl 3-aminopropanoate hydrochloride

CAS58620-93-2

pharmaceutical intermediate

Referencestereoisomer of

(-)-2-amino-1-butanol

CAS5856-63-3

Absorbent

Referencestereoisomer of

2-amino-1-butanol

CAS96-20-8

Metal machining and leather tanning

Safety Reference

Corrosive
Corrosive
Harmful
Harmful
Danger
H302Harmful if swallowed
H314Causes severe skin burns and eye damage

Customs Tariff Classification

The international HS code for (S)-(+)-2-Amino-1-butanol (CAS 5856-62-2) 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-aminobutan-1-ol

InChIKey

JCBPETKZIGVZRE-BYPYZUCNSA-N

SMILES

CC[C@@H](CO)N

Synonyms (10)
  • (+)-2-AMINOBUTANOL
  • (2S)-2-aminobutan-1-ol
  • (S)-(+)-2-Amino-1-butanol
  • (S)-2-aminobutan-1-ol
  • (s)-2-aminobutanol
  • 1-Butanol, 2-amino-, (2S)-
  • 2-(s)-amino-1-butanol
  • 2-Amino-1-butanol, (+)-
  • L-2-Aminobutanol
  • d-(+)2-amino-1-butanol

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