1-Eptadecanolo - ≥97% , CAS No.1454-85-9

CAS: 1454-85-9 Cat. No.: H100266 Formula: C₁₇H₃₆O Peso molecolare: 256.47 Beilstein Registry Number: 1702195 Numero EC: 215-932-5

GRADE & PURITY ≥97%

Synonyms

A884612 | EINECS 215-932-5 | DTXSID3051460 | UNII-N3IL85TMCX | HEPTADECYL ALCOHOL | J-008119 | NCGC00356985-01 | AKOS015899030 | 1-Heptadecanol, purum, >=97.0% (GC) | n-heptadecyl alcohol | AI3-01234 | Q20054528 | Heptadecan-1-ol | n-Heptadecanol | O11822

Storage

Room temperature

Shipped In

Normale

Application

Drug Delivery, Surface Modification, PEGylation of Protein, Peptide & Oligo

Panoramica

Il polimorfismo dell'1-eptadecanolo è stato studiato mediante calorimetria a scansione differenziale (DSC), diffrazione di polveri a raggi X, diffusione Raman e spettroscopia infrarossa (IR).

Specifications

Sinonimi

A884612 | EINECS 215-932-5 | DTXSID3051460 | UNII-N3IL85TMCX | HEPTADECYL ALCOHOL | J-008119 | NCGC00356985-01 | AKOS015899030 | 1-Heptadecanol, purum, >=97.0% (GC) | n-heptadecyl alcohol | AI3-01234 | Q20054528 | Heptadecan-1-ol | n-Heptadecanol | O11822

Specifiche e purezza

≥97%

Condizioni di conservazione di stoccaggio

Room temperature

Spedito in

Normale

Tipo di azione

INHIBITOR

Purezza

≥97%

Nomi e identificatori

• Pubchem Sid: 488182060
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488182060
• Sorrisi canonici: CCCCCCCCCCCCCCCCCO
• IUPAC Name: heptadecan-1-ol
• InChIKey: GOQYKNQRPGWPLP-UHFFFAOYSA-N
• INCHI: 1S/C17H36O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18/h18H,2-17H2,1H3
• Isomeri SMILES: CCCCCCCCCCCCCCCCCO
• WGK Germania: 2
• RTECS: MI3885000
• Peso molecolare: 256.47
• Beilstein: 1702195
• Reaxy-Rn: 1702195
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1702195&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Lipids and lipid-like molecules
    • Classe Fatty Acyls
      • Subclass Fatty alcohols

• Kingdom: Organic compounds
• Superclass: Lipids and lipid-like molecules
• Classe: Fatty Acyls
• Subclass: Fatty alcohols
• Intermediate Tree Nodes: Not available
• Direct Parent: Long-chain fatty alcohols
• Alternative Parents: Primary alcohols Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Long chain fatty alcohol - Organic oxygen compound - Hydrocarbon derivative - Primary alcohol - Organooxygen compound - Alcohol - Aliphatic acyclic compound
• Descrizione: This compound belongs to the class of organic compounds known as long-chain fatty alcohols. These are fatty alcohols that have an aliphatic tail of 13 to 21 carbon atoms.
• External Descriptors: long-chain primary fatty alcohol

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

Obiettivi associati (non umani)

Staphylococcus aureus (210822 Activities)

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

Meccanismi d'azione

Proprietà chimiche e fisiche

• Solubilità: chloroform: soluble 50 mg/mL, clear, colorless
• Punto di infiammabilità (°F): 309.2 °F
• Punto di infiammabilità (°C): 154 ℃
• Punto di ebollizione (°C): 308.5°C
• Punto di fusione (°C): 51-55°C
• Peso molecolare: 256.500 g/mol
• XLogP3: 7.800
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 15
• Exact Mass: 256.277 Da
• Monoisotopic Mass: 256.277 Da
• Topological Polar Surface Area: 20.200 Ų
• Heavy Atom Count: 18
• Formal Charge: 0
• Complexity: 134.000
• 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

Riferimenti

1. Xuwen Zhang, Xuexue Dong, Youting Wang, Juanjuan Bian, Sajid Ali, Dongren Cai, Kang Sun, Xiaoping Rao, Jianchun Jiang, Guowu Zhan.  (2025)  Metal–Organic Frameworks-Derived Cobalt Catalyst Supported on Biochar for Efficient Deoxygenation of Stearic Acid.  INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH,      [PMID:] [10.1021/acs.iecr.4c03679]