(R)-(-)-1-Amino-2-propanol - ≥98%(GC) , CAS No.2799-16-8

CAS: 2799-16-8 Cat. No.: R160942 Molecular Weight: 75.11 EC Number: 220-532-9

GRADE & PURITY ≥98%(GC)

Synonyms

(R)-1-amino 2-propanol | A13190 | AKOS006340931 | 1-Amino-2-propanol # | (2R)-1-amino-2-propanol | A0974 | EINECS 220-532-9 | (R)-1-amino-propan-2-ol | (R)-1-aminopropan-2-ol | (R)-1-Amino-2-propanol | (R)-(-)-1-Amino-2-propanol | DTXSID101318940 | (2R)-1

Storage

Argon charged,Room temperature

Shipped In

Normal

Overview

(R)-(-)-1-Amino-2-propanol is a useful research intermediate used in the synthesis of other bioactive small molecules with pharmaceutical applications.

Specifications

Synonyms

(R)-1-amino 2-propanol | A13190 | AKOS006340931 | 1-Amino-2-propanol # | (2R)-1-amino-2-propanol | A0974 | EINECS 220-532-9 | (R)-1-amino-propan-2-ol | (R)-1-aminopropan-2-ol | (R)-1-Amino-2-propanol | (R)-(-)-1-Amino-2-propanol | DTXSID101318940 | (2R)-1

Specifications & Purity

≥98%(GC)

Storage

Argon charged, Room temperature

Shipped In

Normal

Purity

≥98%(GC)

Names and Identifiers

• Pubchem Sid: 488189757
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488189757
• Canonical Smiles: CC(CN)O
• IUPAC Name: (2R)-1-aminopropan-2-ol
• InChIKey: HXKKHQJGJAFBHI-GSVOUGTGSA-N
• INCHI: 1S/C3H9NO/c1-3(5)2-4/h3,5H,2,4H2,1H3/t3-/m1/s1
• Isomeric SMILES: C[C@H](CN)O
• WGK Germany: 1
• Molecular Weight: 75.11
• Reaxy-Rn: 605275
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=605275&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic nitrogen compounds
    • Class Organonitrogen compounds
      • Subclass Amines
        • Level5 Alkanolamines
          • Level6 1,2-aminoalcohols

• Kingdom: Organic compounds
• Superclass: Organic nitrogen compounds
• Class: Organonitrogen compounds
• Subclass: Amines
• Intermediate Tree Nodes: Alkanolamines
• Direct Parent: 1,2-aminoalcohols
• Alternative Parents: Secondary alcohols Organopnictogen compounds Monoalkylamines Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Secondary alcohol - 1,2-aminoalcohol - Organic oxygen compound - Organopnictogen compound - Hydrocarbon derivative - Primary amine - Organooxygen compound - Primary aliphatic amine - Alcohol - Aliphatic acyclic compound
• Description: This compound belongs to the class of organic compounds known as 1,2-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 C2 atom.
• External Descriptors: Biogenic amines

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

• Sensitivity: Moisture & light & Air sensitive
• Specific Rotation[α]: -24° (C=1,MeOH)
• Flash Point(°F): 159.8 °F
• Flash Point(°C): 71 °C
• Boil Point(°C): 160 °C
• Melt Point(°C): 24 °C
• Molecular Weight: 75.110 g/mol
• XLogP3: -1.000
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 1
• Exact Mass: 75.0684 Da
• Monoisotopic Mass: 75.0684 Da
• Topological Polar Surface Area: 46.300 Ų
• Heavy Atom Count: 5
• Formal Charge: 0
• Complexity: 22.900
• 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. Hai-Min Shen, Hong-Bing Ji.  (2013)  Cyclodextrin–[RuCl2(Arene)]2 conjugates: another way to enhance the enantioselectivity of aromatic ketones reduction by aromatic ligands' volume.  TETRAHEDRON,      [PMID:] [10.1016/j.tet.2013.07.077]

2. Ningbo Yu, Shaofei Wang, Min Zhou, Min Xiao, Bo Jin, Hongxia Gao, Zhiwu Liang.  (2026)  Unveiling solvent encapsulation-driven kinetic inversion in CO2 absorption by water-lean amine solvents.  AICHE JOURNAL,      [PMID:] [10.1002/aic.70260]