10-Undecen-1-ol - ≥98% , CAS No.112-43-6

CAS: 112-43-6 Cat. No.: U106482 Formula: C₁₁H₂₂O Peso molecolare: 170.29 Beilstein Registry Number: 1753225 Numero EC: 203-971-0

GRADE & PURITY ≥98%

Synonyms

omega-Undecylenyl alcohol | 10-Undecylen-1-ol | undec-10-en-1-ol | WLN: Q10U1 | 1-Undecen-11-ol | Q18611668 | omega-undecylenyl alcoho | SY011350 | Undec-10-enol | omega-Undecenyl alcohol | AI3-06259 | AKOS015903579 | DTXSID4059419 | .OMEGA.-UNDECENOL | 1

Storage

Room temperature

Shipped In

Normal

Application

228,229

Panoramica

application：

10-Undecen-1-ol is used as a flavoring agent. It reacts with tosylated beta-cyclodextrin to prepare beta-cyclodextrin undecenylether. It is used in the synthesis of 10-Undecenylacrylat by reacting with acryloyl and triethylamine. It reacts with carbon monoxide in the presence of dicobalt octacarbonyl and pyridine as a base at pressures greater than 150 bar and temperatures in the range of 100 to 2000C to linear and branched polyesters having relatively high molecular weights (Mn> 10,000 g / mol) in good yields.

Specifications

Sinonimi

omega-Undecylenyl alcohol | 10-Undecylen-1-ol | undec-10-en-1-ol | WLN: Q10U1 | 1-Undecen-11-ol | Q18611668 | omega-undecylenyl alcoho | SY011350 | Undec-10-enol | omega-Undecenyl alcohol | AI3-06259 | AKOS015903579 | DTXSID4059419 | .OMEGA.-UNDECENOL | 1

Specifiche e purezza

≥98%

Condizioni di conservazione di stoccaggio

Room temperature

Spedito in

Normal

Purezza

≥98%

Nomi e identificatori

• Pubchem Sid: 488180722
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488180722
• Sorrisi canonici: C=CCCCCCCCCCO
• IUPAC Name: undec-10-en-1-ol
• InChIKey: GIEMHYCMBGELGY-UHFFFAOYSA-N
• INCHI: 1S/C11H22O/c1-2-3-4-5-6-7-8-9-10-11-12/h2,12H,1,3-11H2
• Isomeri SMILES: C=CCCCCCCCCCO
• WGK Germania: 2
• RTECS: YQ2985000
• Peso molecolare: 170.29
• Beilstein: 1753225
• Reaxy-Rn: 1753225

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: Primary alcohols Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: 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 fatty alcohols. These are aliphatic alcohols consisting of a chain of a least six carbon atoms.
• 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

Proprietà chimiche e fisiche

• Solubilità: Miscible with alcohol and ether. Immiscible with water
• Indice di rifrazione: 1.446-1.453
• Punto di infiammabilità (°F): 257 °F
• Punto di infiammabilità (°C): 125℃
• Punto di ebollizione (°C): 245-248°C
• Punto di fusione (°C): -3°C
• Peso molecolare: 170.290 g/mol
• XLogP3: 4.800
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 9
• Exact Mass: 170.167 Da
• Monoisotopic Mass: 170.167 Da
• Topological Polar Surface Area: 20.200 Ų
• Heavy Atom Count: 12
• Formal Charge: 0
• Complexity: 89.000
• 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. Xuan Xin, Mengmeng Zhang, Xiao-Feng Li, Guanglei Zhao.  (2019)  Biocatalytic Synthesis of Lipophilic Baicalin Derivatives as Antimicrobial Agents.  JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY,      [PMID:31564105] [10.1021/acs.jafc.9b04667]

2. Changchang Zhang, Yong Kuai, Heming Cheng, Xiang Liu, Liang Ma.  (2017)  Covalent bonding of grafted polymer brushes of poly(poly(ethylene glycol) monomethacrylate) on surface of silicon quantum dots and the activation of the end hydroxyls.  Arabian Journal of Chemistry,      [PMID:] [10.1016/j.arabjc.2016.12.022]

3. Chenyang Xia, Bowen Lu, Qi Xu, Nanxin Shen, Qiancheng Liao, Jiyun Cui, Baiyang Wang, Yueyang Sun, Changjiang Dong, Fei Gan.  (2025)  Structural and Mechanistic Insights into Dual Deprotonation by an Engineered GPP Methyltransferase: Discovery of Methyltransferases Generating Noncanonical Prenyl Diphosphates.  ACS Catalysis,      [PMID:] [10.1021/acscatal.5c03939]

Domande frequenti

What is the purity of this product?

This product is supplied at ≥98% purity (chemical assay). 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 112-43-6, the molecular formula is C11H22O, and the molecular weight is 170.29 g/mol. InChIKey GIEMHYCMBGELGY-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.