Anidrido palmítico - ≥96% , CAS No.623-65-4

CAS: 623-65-4 Cat. No.: P160066 Fórmula: C₃₂H₆₂O₃ Peso molecular: 494.85 Beilstein Registry Number: 1807510 Número CE: 210-805-0 PubChem CID: 69339

GRADE & PURITY ≥96%

Synonyms

HY-W093183 | Palmitic anhydride | n-hexadecanoic anhydride | SCHEMBL149967 | AKOS016013112 | FT-0632621 | 2-(4-METHOXY-PHENYLAMINO)-4-NITRO-BENZOICACID | hexadecanoyl hexadecanoate | NSC 285112 | P0008 | hexadecanoic acid anhydride | Hexadecanoic anhydrid

Storage

Argon charged,Room temperature

Shipped In

Normal

Visão geral

Reagiu com 20-metil espirolida G para formar um derivado com um tempo de retenção e espetro idênticos ao metabolito, 17-O-palmitoil-20-metil espirolida G.
Foi utilizado na síntese de N-palmitoilquitosano (PLCS) solúvel em água por acoplamento com quitosano inchado em dimetilsulfóxido (DMSO). Foi também utilizado na síntese de N-acilfosfatidilserina.

Specifications

Sinónimos

HY-W093183 | Palmitic anhydride | n-hexadecanoic anhydride | SCHEMBL149967 | AKOS016013112 | FT-0632621 | 2-(4-METHOXY-PHENYLAMINO)-4-NITRO-BENZOICACID | hexadecanoyl hexadecanoate | NSC 285112 | P0008 | hexadecanoic acid anhydride | Hexadecanoic anhydrid

Especificações e pureza

≥96%

Condições de armazenamento de armazenamento

Argon charged,Room temperature

Enviado em

Normal

Pureza

≥96%

Nomes e identificadores

Pubchem Sid

488184295

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/488184295

Sorrisos canónicos

CCCCCCCCCCCCCCCC(=O)OC(=O)CCCCCCCCCCCCCCC

IUPAC Name

hexadecanoyl hexadecanoate

InChIKey

QWZBEFCPZJWDKC-UHFFFAOYSA-N

INCHI

1S/C32H62O3/c1-3-5-7-9-11-13-15-17-19-21-23-25-27-29-31(33)35-32(34)30-28-26-24-22-20-18-16-14-12-10-8-6-4-2/h3-30H2,1-2H3

SMILES isoméricas

CCCCCCCCCCCCCCCC(=O)OC(=O)CCCCCCCCCCCCCCC

WGK Alemanha

3

PubChem CID

69339

Peso molecular

494.85

Beilstein

1807510

Reaxy-Rn

1807507

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • Classe Carboxylic acids and derivatives
      • Subclass Dicarboxylic acids and derivatives

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Classe: Carboxylic acids and derivatives
• Subclass: Dicarboxylic acids and derivatives
• Intermediate Tree Nodes: Not available
• Direct Parent: Dicarboxylic acids and derivatives
• Alternative Parents: Carboxylic acid anhydrides Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Dicarboxylic acid or derivatives - Carboxylic acid anhydride - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aliphatic acyclic compound
• Descrição: This compound belongs to the class of organic compounds known as dicarboxylic acids and derivatives. These are organic compounds containing exactly two carboxylic acid groups.
• 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

Propriedades químicas e físicas

• Sensibilidade: Moisture Sensitive
• Ponto de fusão (°C): 64 °C
• Peso molecular: 494.800 g/mol
• XLogP3: 14.600
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 30
• Exact Mass: 494.47 Da
• Monoisotopic Mass: 494.47 Da
• Topological Polar Surface Area: 43.400 Ų
• Heavy Atom Count: 35
• Formal Charge: 0
• Complexity: 406.000
• 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