(S)-(+)-1-Amino-2-propanol - ≥97%(GC) , CAS No.2799-17-9

CAS: 2799-17-9 Cat. No.: S161024 Peso molecular: 75.11 Número EC: 220-533-4

GRADE & PURITY ≥97%(GC)

Synonyms

(S)-1-(aminomethyl)ethan-1-ol | A0975 | CL0074 | (S)-(+)-1-Aminopropan-2-ol | STR07322 | (S)-1-amino 2-propanol | 3,5-Dichloro-4(1H)-pyridinone # | (S)-(+)-Isopropanolamine | (S)-2-hyroxypropylamine | 1-Amino-2-propanol # | EINECS 220-533-4 | F-LOOP OF VI

Storage

Store at 2-8°C,Argon charged

Shipped In

Wet ice

Descripción general

(S)-(+)-1-Amino-2-propanol is a chiral amino alcohol.

Specifications

Sinónimos

(S)-1-(aminomethyl)ethan-1-ol | A0975 | CL0074 | (S)-(+)-1-Aminopropan-2-ol | STR07322 | (S)-1-amino 2-propanol | 3, 5-Dichloro-4(1H)-pyridinone # | (S)-(+)-Isopropanolamine | (S)-2-hyroxypropylamine | 1-Amino-2-propanol # | EINECS 220-533-4 | F-LOOP OF VI

Especificaciones y pureza

≥97%(GC)

Condiciones de almacenamiento de almacenamiento

Store at 2-8°C, Argon charged

Enviado en

Wet ice

Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.

Pureza

≥97%(GC)

Nombres e identificadores

• Sonrisas canónicas: CC(CN)O
• IUPAC Name: (2S)-1-aminopropan-2-ol
• InChIKey: HXKKHQJGJAFBHI-VKHMYHEASA-N
• INCHI: 1S/C3H9NO/c1-3(5)2-4/h3,5H,2,4H2,1H3/t3-/m0/s1
• Isómeros SMILES: C[C@@H](CN)O
• WGK Alemania: 1
• Peso molecular: 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
    • Clase Organonitrogen compounds
      • Subclass Amines
        • Level5 Alkanolamines
          • Level6 1,2-aminoalcohols

• Kingdom: Organic compounds
• Superclass: Organic nitrogen compounds
• Clase: Organonitrogen compounds
• Subclass: Amines
• Intermediate Tree Nodes: Alkanolamines
• Direct Parent: 1,2-aminoalcohols
• Alternative Parents: Secondary alcohols Monoalkylamines Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Secondary alcohol - 1,2-aminoalcohol - Organic oxygen compound - Hydrocarbon derivative - Primary amine - Organooxygen compound - Primary aliphatic amine - Alcohol - Aliphatic acyclic compound
• Descripción: 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: 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

Propiedades químicas y físicas

• Solubilidad: Soluble in water; Soluble in Ether,Alcohol,Acetone
• Sensibilidad: Air & Moisture Sensitive
• Índice de refracción: n20/D 1.4437
• Rotación específica [α]: [α]20/D +18°, c = 1.8 in H2O
• Punto de inflamación (°F): 159.8 °F
• Punto de inflamación (°C): 71 °C
• Punto de ebullición (°C): 160 °C
• Punto de fusión (°C): 24-26°C
• Peso molecular: 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

Referencias

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. Hai-Min Shen, Hong-Bing Ji.  (2012)  Amino alcohol-modified β-cyclodextrin inducing biomimetic asymmetric oxidation of thioanisole in water.  CARBOHYDRATE RESEARCH,      [PMID:22541298] [10.1016/j.carres.2012.03.034]