2-Undecanol - ≥98%(GC) , CAS No.1653-30-1

CAS: 1653-30-1 Cat. No.: U162921 Formula: C₁₁H₂₄O Peso molecolare: 172.31 Numero EC: 216-722-6 PubChem CID: 15448

GRADE & PURITY ≥98%(GC)

Synonyms

DL-2-Undecanol | AKOS009159106 | FEMA 3246 | SCHEMBL378851 | CHEBI:77930 | Methyl nonyl carbinol | 2-Hydroxyundecane | (+/-)-2-UNDECANOL | 49PCZ1S7LY | FEMA No. 3246 | FT-0613465 | BAA65330 | U0027 | 2-UNDECANOL | SY048567 | (+)-2-Undecanol | D92751 | Und

Storage

Room temperature

Shipped In

Normal

Panoramica

2-Undecanol is a volatile fatty alcohol that is reported to occur as a flavor component of coconut meat, cheese and hopped beer.

Specifications

Sinonimi

DL-2-Undecanol | AKOS009159106 | FEMA 3246 | SCHEMBL378851 | CHEBI:77930 | Methyl nonyl carbinol | 2-Hydroxyundecane | (+/-)-2-UNDECANOL | 49PCZ1S7LY | FEMA No. 3246 | FT-0613465 | BAA65330 | U0027 | 2-UNDECANOL | SY048567 | (+)-2-Undecanol | D92751 | Und

Specifiche e purezza

≥98%(GC)

Condizioni di conservazione di stoccaggio

Room temperature

Spedito in

Normal

Purezza

≥98%(GC)

Nomi e identificatori

• Pubchem Sid: 488182123
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488182123
• Sorrisi canonici: CCCCCCCCCC(C)O
• IUPAC Name: undecan-2-ol
• InChIKey: XMUJIPOFTAHSOK-UHFFFAOYSA-N
• INCHI: 1S/C11H24O/c1-3-4-5-6-7-8-9-10-11(2)12/h11-12H,3-10H2,1-2H3
• Isomeri SMILES: CCCCCCCCCC(C)O
• WGK Germania: 2
• PubChem CID: 15448
• Peso molecolare: 172.31
• Reaxy-Rn: 1719795

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: Fatty alcohols
• Alternative Parents: Secondary alcohols Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Fatty alcohol - Secondary alcohol - Organic oxygen compound - Hydrocarbon derivative - Organooxygen compound - Alcohol - Aliphatic acyclic compound
• Descrizione: This compound belongs to the class of organic compounds known as fatty alcohols. These are aliphatic alcohols consisting of a chain of a least six carbon atoms.
• External Descriptors: 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

Meccanismi d'azione

Proprietà chimiche e fisiche

• Solubilità: Not miscible or difficult to mix in water. Soluble in alcohol and ethyl ether.
• Indice di rifrazione: 1.44
• Punto di infiammabilità (°F): 225°F
• Punto di infiammabilità (°C): 107℃
• Punto di ebollizione (°C): 228-229℃
• Punto di fusione (°C): 1-3℃
• Peso molecolare: 172.310 g/mol
• XLogP3: 4.500
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 8
• Exact Mass: 172.183 Da
• Monoisotopic Mass: 172.183 Da
• Topological Polar Surface Area: 20.200 Ų
• Heavy Atom Count: 12
• Formal Charge: 0
• Complexity: 81.100
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 1
• 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. Hongyu Chen, Ronggang Jiang, Huimin An, Hao Xu, Xingchang Ou, Kuofei Wang, Yuan Chen, Youcang Jiang, Shi Li, Jianan Huang, Zhonghua Liu.  (2026)  Characterization of key odor-active volatiles in jasmine green tea by sensomics and chemometrics.  Food Chemistry-X,      [PMID:41799623] [10.1016/j.fochx.2026.103695]