Propionato de isobutilo - ≥98%(GC) , CAS No.540-42-1

CAS: 540-42-1 Cat. No.: I157498 Peso molecular: 130.19 Beilstein Registry Number: 2(4)709 Número EC: 208-746-0

GRADE & PURITY ≥98%(GC)

Synonyms

LMFA07010567 | CHEBI:88813 | Propionato de isobutilo | Propionato de isobutilo [UN2394] [Líquido inflamable] | Q27160785 | SCHEMBL124736 | Propionato de 2-metilpropilo | FT-0627364 | AI3-28238 | NSC 8450 | FEMA No. 2212 | PROPIONATO DE ISOBUTILO [MI] | Pr

Storage

Room temperature

Shipped In

FedEx DG Service

Specifications

Sinónimos

LMFA07010567 | CHEBI:88813 | Propionato de isobutilo | Propionato de isobutilo [UN2394] [Líquido inflamable] | Q27160785 | SCHEMBL124736 | Propionato de 2-metilpropilo | FT-0627364 | AI3-28238 | NSC 8450 | FEMA No. 2212 | PROPIONATO DE ISOBUTILO [MI] | Pr

Especificaciones y pureza

≥98%(GC)

Condiciones de almacenamiento de almacenamiento

Room temperature

Enviado en

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Pureza

≥98%(GC)

Nombres e identificadores

• Pubchem Sid: 488181217
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488181217
• Sonrisas canónicas: CCC(=O)OCC(C)C
• IUPAC Name: 2-methylpropyl propanoate
• InChIKey: FZXRXKLUIMKDEL-UHFFFAOYSA-N
• INCHI: 1S/C7H14O2/c1-4-7(8)9-5-6(2)3/h6H,4-5H2,1-3H3
• Isómeros SMILES: CCC(=O)OCC(C)C
• WGK Alemania: 2
• RTECS: UF4930000
• Número ONU: 2394
• Grupo de embalaje: III
• Peso molecular: 130.19
• Beilstein: 2(4)709
• Reaxy-Rn: 1745554
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1745554&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • Clase Carboxylic acids and derivatives
      • Subclass Carboxylic acid derivatives

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Clase: Carboxylic acids and derivatives
• Subclass: Carboxylic acid derivatives
• Intermediate Tree Nodes: Not available
• Direct Parent: Carboxylic acid esters
• Alternative Parents: Monocarboxylic acids and derivatives Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Carboxylic acid ester - Monocarboxylic acid or derivatives - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aliphatic acyclic compound
• Descripción: This compound belongs to the class of organic compounds known as carboxylic acid esters. These are carboxylic acid derivatives in which the carbon atom from the carbonyl group is attached to an alkyl or an aryl moiety through an oxygen atom (forming an ester group).
• External Descriptors: Wax monoesters

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

• Índice de refracción: 1.4
• Punto de inflamación (°F): 78.8 °F
• Punto de inflamación (°C): 26 °C
• Punto de ebullición (°C): 138 °C
• Peso molecular: 130.180 g/mol
• XLogP3: 2.200
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 4
• Exact Mass: 130.099 Da
• Monoisotopic Mass: 130.099 Da
• Topological Polar Surface Area: 26.300 Ų
• Heavy Atom Count: 9
• Formal Charge: 0
• Complexity: 86.900
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• 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