2-Pentadecanona - ≥95%(GC) , CAS No.2345-28-0

CAS: 2345-28-0 Cat. No.: P160486 Fórmula: C₁₅H₃₀O Peso molecular: 226.4 Número CE: 219-064-8 PubChem CID: 61303

GRADE & PURITY ≥95%(GC)

Synonyms

D92066 | B2Q48J997N | CAA34528 | DTXSID6062333 | A878236 | Pentadecanone | AKOS009157795 | J-015112 | AI3-11706 | 2-Pentandecanone | Methyl tridecyl ketone | FT-0613261 | AS-56748 | 2-PENTADECANONE | Pentadecan-2-one | 2-Pentadecanone, >=98.5% | EINECS 21

Storage

Room temperature

Shipped In

Normal

Visão geral

aplicação：

É usado principalmente como uma substância aromatizante para conferir um sabor gordo, ligeiramente picante e floral. a 2-Pentadecanona pode complementar e melhorar perfeitamente uma variedade de alimentos, incluindo manteigas, queijos e carnes.

Specifications

Sinónimos

D92066 | B2Q48J997N | CAA34528 | DTXSID6062333 | A878236 | Pentadecanone | AKOS009157795 | J-015112 | AI3-11706 | 2-Pentandecanone | Methyl tridecyl ketone | FT-0613261 | AS-56748 | 2-PENTADECANONE | Pentadecan-2-one | 2-Pentadecanone, >=98.5% | EINECS 21

Especificações e pureza

≥95%(GC)

Condições de armazenamento de armazenamento

Room temperature

Enviado em

Normal

Tipo de ação

INHIBITOR

Pureza

≥95%(GC)

Nomes e identificadores

• Pubchem Sid: 488183479
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488183479
• Sorrisos canónicos: CCCCCCCCCCCCCC(=O)C
• IUPAC Name: pentadecan-2-one
• InChIKey: CJPNOLIZCWDHJK-UHFFFAOYSA-N
• INCHI: 1S/C15H30O/c1-3-4-5-6-7-8-9-10-11-12-13-14-15(2)16/h3-14H2,1-2H3
• SMILES isoméricas: CCCCCCCCCCCCCC(=O)C
• WGK Alemanha: 3
• PubChem CID: 61303
• Peso molecular: 226.4
• Reaxy-Rn: 1764872

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic oxygen compounds
    • Classe Organooxygen compounds
      • Subclass Carbonyl compounds

• Kingdom: Organic compounds
• Superclass: Organic oxygen compounds
• Classe: Organooxygen compounds
• Subclass: Carbonyl compounds
• Intermediate Tree Nodes: Not available
• Direct Parent: Ketones
• Alternative Parents: Organic oxides Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Ketone - Organic oxide - Hydrocarbon derivative - Aliphatic acyclic compound
• Descrição: This compound belongs to the class of organic compounds known as ketones. These are organic compounds in which a carbonyl group is bonded to two carbon atoms R2C=O (neither R may be a hydrogen atom). Ketones that have one or more alpha-hydrogen atoms undergo keto-enol tautomerization, the tautomer being an enol.
• External Descriptors: a ketone

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

Alvos associados (não humanos)

Rattus norvegicus (775804 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Mecanismos de ação

Propriedades químicas e físicas

• Solubilidade: Soluble in toluene (almost transparency). Insoluble in water.
• Ponto de inflamação (°F): 235.4 °F
• Ponto de inflamação (°C): 113 °C
• Ponto de ebulição (°C): 293℃
• Ponto de fusão (°C): 39℃
• Peso molecular: 226.400 g/mol
• XLogP3: 6.300
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 12
• Exact Mass: 226.23 Da
• Monoisotopic Mass: 226.23 Da
• Topological Polar Surface Area: 17.100 Ų
• Heavy Atom Count: 16
• Formal Charge: 0
• Complexity: 152.000
• 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

Referências

1. Chengrui Liang, Shuxiao Wang, Bin Zhao, Boyang Feng, Qipeng Qu, Liang Zhu, Jiming Hao.  (2025)  Impact of Molecular Structure on Secondary Organic Aerosol Formation from Aliphatic Carbonyls.  ENVIRONMENTAL SCIENCE & TECHNOLOGY,      [PMID:40552609] [10.1021/acs.est.5c00793]

2. Qingfu Wang, Jiaming Zhao, Zening Wang, Liuke Zhang, Lei Li, Yibo Ning, Zhipeng Jing, Pengfei Yang, Yongzhen Zhao, Changtong Lu.  (2026)  Study on the enhancement of volatile components extraction from Lysimachia foenum-graecum Hance essential oil by metal salts.  Frontiers in Chemistry,      [PMID:42482699] [10.3389/fchem.2026.1869613]

Perguntas frequentes

What is the purity of this product, and how is it determined?

This product is supplied at ≥95% purity, determined by gas chromatography (GC). Lot-specific values are stated on the Certificate of Analysis.

How should this product be stored?

Store at room temperature.

How is this product shipped?

This product ships under standard ambient conditions. No temperature-controlled packaging is required.

What are the CAS number, molecular formula and molecular weight?

The CAS Number is 2345-28-0, the molecular formula is C15H30O, and the molecular weight is 226.4 g/mol. InChIKey CJPNOLIZCWDHJK-UHFFFAOYSA-N.

What documentation is provided?

Available product documentation, including Certificates of Analysis (COA), Safety Data Sheets (SDS), and specification sheets, is shown in the product document area. Document availability and access follow the current site policy.