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

CAS: 1454-85-9 Cat. No.: H100266 Summenformel: C₁₇H₃₆O Molekulargewicht: 256.47 Beilstein Registry Number: 1702195 EG-Nummer: 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

Normal

Application

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

Übersicht

The polymorphism of 1-heptadecanol was studied by differential scanning calorimetry (DSC), X-ray powder diffraction, Raman scattering and infrared spectroscopy (IR).

Specifications

Synonyme

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

Spezifikationen & Reinheit

≥97%

Storage

Room temperature

Verschickt in

Normal

Aktionsart

INHIBITOR

Reinheit

≥97%

Namen und Kennungen

• Pubchem Sid: 488182060
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488182060
• Kanonisches Lächeln: 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
• Isomere SMILES: CCCCCCCCCCCCCCCCCO
• WGK Deutschland: 2
• RTECS: MI3885000
• Molekulargewicht: 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
    • Klasse Fatty Acyls
      • Subclass Fatty alcohols

• Kingdom: Organic compounds
• Superclass: Lipids and lipid-like molecules
• Klasse: 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
• Beschreibung: 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

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Staphylococcus aureus (210822 Activities)

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Wirkungsmechanismen

Chemische und physikalische Eigenschaften

• Löslichkeit: chloroform: soluble 50 mg/mL, clear, colorless
• Flammpunkt (°F): 309.2 °F
• Flammpunkt (°C): 154 ℃
• Siedepunkt (°C): 308.5°C
• Schmelzpunkt (°C): 51-55°C
• Molekulargewicht: 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

Referenzen

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]