(R)-3-Aminobutanol - ≥98% , CAS No.61477-40-5

CAS: 61477-40-5 Cat. No.: A123608 Molecular Weight: 89.14 EC Number: 640-387-9

GRADE & PURITY ≥98%

Synonyms

AGMZSYQMSHMXLT-SCSAIBSYSA-N | GS-3850 | BCP01279 | W-204235 | AM9719 | (R)-3-amino-butan-1-ol | (R)-3-aminobutan-1-ol | (3R)-3-Amino-1-butanol | (R)-3-AMINO-1-BUTANOL | R-3-amino-1-butanol | A15693 | 1-Butanol, 3-amino-, (R)- | DTXSID30432476 | (R,S)-3-Am

Storage

Room temperature

Shipped In

Normal

Specifications

Synonyms

AGMZSYQMSHMXLT-SCSAIBSYSA-N | GS-3850 | BCP01279 | W-204235 | AM9719 | (R)-3-amino-butan-1-ol | (R)-3-aminobutan-1-ol | (3R)-3-Amino-1-butanol | (R)-3-AMINO-1-BUTANOL | R-3-amino-1-butanol | A15693 | 1-Butanol, 3-amino-, (R)- | DTXSID30432476 | (R, S)-3-Am

Specifications & Purity

≥98%

Storage

Room temperature

Shipped In

Normal

Purity

≥98%

Names and Identifiers

• Pubchem Sid: 488196413
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488196413
• Canonical Smiles: CC(CCO)N
• IUPAC Name: (3R)-3-aminobutan-1-ol
• InChIKey: AGMZSYQMSHMXLT-SCSAIBSYSA-N
• INCHI: 1S/C4H11NO/c1-4(5)2-3-6/h4,6H,2-3,5H2,1H3/t4-/m1/s1
• Isomeric SMILES: C[C@H](CCO)N
• UN Number: 2734
• Packing Group: II
• Molecular Weight: 89.14
• Reaxy-Rn: 1731402
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1731402&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic nitrogen compounds
    • Class Organonitrogen compounds
      • Subclass Amines
        • Level5 Alkanolamines
          • Level6 1,3-aminoalcohols

• Kingdom: Organic compounds
• Superclass: Organic nitrogen compounds
• Class: Organonitrogen compounds
• Subclass: Amines
• Intermediate Tree Nodes: Alkanolamines
• Direct Parent: 1,3-aminoalcohols
• Alternative Parents: Primary alcohols Monoalkylamines Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: 1,3-aminoalcohol - Organic oxygen compound - Hydrocarbon derivative - Primary amine - Primary alcohol - Organooxygen compound - Primary aliphatic amine - Alcohol - Aliphatic acyclic compound
• Description: This compound belongs to the class of organic compounds known as 1,3-aminoalcohols. These are organic compounds containing an alkyl chain with an amine group bound to the C1 atom and an alcohol group bound to the C3 atom.
• External Descriptors: Not available

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Chemical and Physical Properties

• Refractive Index: 1.45
• Specific Rotation[α]: -10° (C=1,EtOH)
• Flash Point(°C): 56 °C
• Boil Point(°C): 168°C
• Molecular Weight: 89.140 g/mol
• XLogP3: -0.600
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 2
• Exact Mass: 89.0841 Da
• Monoisotopic Mass: 89.0841 Da
• Topological Polar Surface Area: 46.300 Ų
• Heavy Atom Count: 6
• Formal Charge: 0
• Complexity: 30.700
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 1
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1

References

1. Xiao-Ling Tang, Nan-Nan Zhang, Guo-Yan Ye, Yu-Guo Zheng.  (2019)  Efficient biosynthesis of (R)-3-amino-1-butanol by a novel (R)-selective transaminase from Actinobacteria sp..  JOURNAL OF BIOTECHNOLOGY,      [PMID:30853639] [10.1016/j.jbiotec.2019.02.008]

2. Qi Gu, Kefan Chen, Xiong Zhang, Shuaihua Wang, Shaofan Wu, Wanxia Huang.  (2025)  Butylammonium-Based Chiral 2D Perovskite Single Crystals for Efficient UV Circularly Polarized Light Differentiation and High-Performance X-ray Detection.  ACS Applied Materials & Interfaces,      [PMID:40047434] [10.1021/acsami.5c01035]