2-Hexyl-1-decanol - ≥97%, used for 2-Hexyl-1-decanol may be employed as an organic solvent to study the extraction of non-polar acidic drugs from human plasma by parallel artificial liquid membrane extraction (PALME). various applications , CAS No.2425-77

CAS: 2425-77-6 Cat. No.: H138544 Summenformel: CH₃(CH₂)₇CH[(CH₂)₅CH₃]CH₂OH Molekulargewicht: 242.44 EG-Nummer: 219-370-1

GRADE & PURITY ≥97%

Synonyms

HEXYLDECANOL [INCI] | Rilanit G 16 | 151Z7P1317 | NJCOL 160BR | Guerbitol 16 | AI3-19964 | NSC 2399 | A877978 | NJCOL 160BRA | MFCD00060903 | F11131 | NJCOL 160 | .alpha.-chloralose | CAS-2425-77-6 | EC 219-370-1 | SY034340 | AKOS015912415 | Guerbet C16 |

Storage

Room temperature

Shipped In

Normal

Übersicht

2-Hexyl-1-decanol is a branched alcohol. It is one of the constituent of the essential oil, extracted from the roots of Adiantum flabellulatum. It is a long-chain glass forming monohydroxy alcohol and its dielectric relaxation at low temperature has been studied.

Specifications

Synonyme

HEXYLDECANOL [INCI] | Rilanit G 16 | 151Z7P1317 | NJCOL 160BR | Guerbitol 16 | AI3-19964 | NSC 2399 | A877978 | NJCOL 160BRA | MFCD00060903 | F11131 | NJCOL 160 | .alpha.-chloralose | CAS-2425-77-6 | EC 219-370-1 | SY034340 | AKOS015912415 | Guerbet C16 |

Spezifikationen & Reinheit

≥97%

Anmeldung

2-Hexyl-1-decanol may be employed as an organic solvent to study the extraction of non-polar acidic drugs from human plasma by parallel artificial liquid membrane extraction (PALME).

Storage

Room temperature

Verschickt in

Normal

Reinheit

≥97%

Namen und Kennungen

• Pubchem Sid: 504756263
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504756263
• Kanonisches Lächeln: CCCCCCCCC(CCCCCC)CO
• IUPAC Name: 2-hexyldecan-1-ol
• InChIKey: XULHFMYCBKQGEE-UHFFFAOYSA-N
• INCHI: 1S/C16H34O/c1-3-5-7-9-10-12-14-16(15-17)13-11-8-6-4-2/h16-17H,3-15H2,1-2H3
• Isomere SMILES: CCCCCCCCC(CCCCCC)CO
• Molekulargewicht: 242.44
• Reaxy-Rn: 1748375
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1748375&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: 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
• Beschreibung: 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

Chemische und physikalische Eigenschaften

• Brechungsindex: 1.449
• Flammpunkt (°F): 318.2 °F
• Flammpunkt (°C): 159 °C
• Siedepunkt (°C): 193-197 °C/33 mmHg
• Schmelzpunkt (°C): -21~-15°C
• Molekulargewicht: 242.440 g/mol
• XLogP3: 7.000
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 13
• Exact Mass: 242.261 Da
• Monoisotopic Mass: 242.261 Da
• Topological Polar Surface Area: 20.200 Ų
• Heavy Atom Count: 17
• Formal Charge: 0
• Complexity: 133.000
• 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

Referenzen

1. Hezhen Xu, Shiyi Zuo, Danping Wang, Yu Zhang, Wenxiao Li, Lingxiao Li, Tian Liu, Yuanhao Yu, Qingzhi Lv, Zhonggui He, Jin Sun, Bingjun Sun.  (2023)  Cabazitaxel prodrug nanoassemblies with branched chain modifications: Narrowing the gap between efficacy and safety.  JOURNAL OF CONTROLLED RELEASE,      [PMID:37451544] [10.1016/j.jconrel.2023.07.012]

2. Jian Yang, Jiangtao Wu, Shengshan Bi.  (2021)  Surface Tension Measurements by Pendant Drop Method of 10 Pure Long-Chain Alkanes and Alcohols for Temperatures up to 573.15 K.  JOURNAL OF CHEMICAL AND ENGINEERING DATA,      [PMID:] [10.1021/acs.jced.1c00212]

3. Xuejiao Song, Zexiang Bi, Zimeng Wei, Xu Li, Jinxiang Dong.  (2025)  Branched-chain anionic surfactants with same hydrophobic tail architecture: effects of hydrophilic headgroups.  TENSIDE SURFACTANTS DETERGENTS,      [PMID:] [10.1515/tsd-2024-2639]