1H,1H,2H,2H-Perfluorohexan-1-ol - ≥98% , CAS No.2043-47-2

CAS: 2043-47-2 Cat. No.: P122276 Molecular Weight: 264.09 EC Number: 218-050-9

GRADE & PURITY ≥98%

Synonyms

C6H5F9O | MFCD00039543 | 2-Naphthalenol, 1-(1-piperidinylmethyl)- | 2-Octyl dodecanol | 2-perfluorobutyl ethanol (4:2) | 1h,1h,2h,2h-nonafluorohexan-1-ol | N0600 | 4:2 FTOH | 1H, 1H, 2H, 2H-perfluorohexan-1-ol, 98% | AS-48920 | n:2 fluorotelomer alcohols,

Storage

Argon charged,Room temperature

Shipped In

Normal

Overview

application：

1H,1H,2H,2H-Perfluorohexanol is used in the synthesis of polymer coatings with controlled surface topography. As well used in the preparation of star polymers as fluorous nanocapsules for the encapsulation and release of perfluorinated compounds.

Specifications

Synonyms

C6H5F9O | MFCD00039543 | 2-Naphthalenol, 1-(1-piperidinylmethyl)- | 2-Octyl dodecanol | 2-perfluorobutyl ethanol (4:2) | 1h, 1h, 2h, 2h-nonafluorohexan-1-ol | N0600 | 4:2 FTOH | 1H, 1H, 2H, 2H-perfluorohexan-1-ol, 98% | AS-48920 | n:2 fluorotelomer alcohols,

Specifications & Purity

≥98%

Storage

Argon charged, Room temperature

Shipped In

Normal

Purity

≥98%

Names and Identifiers

• Pubchem Sid: 504754880
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504754880
• Canonical Smiles: C(CO)C(C(C(C(F)(F)F)(F)F)(F)F)(F)F
• IUPAC Name: 3,3,4,4,5,5,6,6,6-nonafluorohexan-1-ol
• InChIKey: JCMNMOBHVPONLD-UHFFFAOYSA-N
• INCHI: 1S/C6H5F9O/c7-3(8,1-2-16)4(9,10)5(11,12)6(13,14)15/h16H,1-2H2
• Isomeric SMILES: C(CO)C(C(C(C(F)(F)F)(F)F)(F)F)(F)F
• WGK Germany: 3
• Molecular Weight: 264.09
• Reaxy-Rn: 2095198
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2095198&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organohalogen compounds
    • Class Alkyl halides
      • Subclass Alkyl fluorides

• Kingdom: Organic compounds
• Superclass: Organohalogen compounds
• Class: Alkyl halides
• Subclass: Alkyl fluorides
• Intermediate Tree Nodes: Not available
• Direct Parent: Fluorotelomer alcohols
• Alternative Parents: Primary alcohols Organofluorides Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Fluorotelomer alcohol - Organic oxygen compound - Hydrocarbon derivative - Primary alcohol - Organooxygen compound - Organofluoride - Alcohol - Aliphatic acyclic compound
• Description: This compound belongs to the class of organic compounds known as fluorotelomer alcohols. These are fluorocarbon-based oligomers linked to an alcohol chain.
• 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

Chemical and Physical Properties

• Sensitivity: Heat sensitive；Air sensitive
• Refractive Index: 1.314
• Flash Point(°F): 163.4 °F
• Flash Point(°C): 73°C(Lit.)
• Boil Point(°C): 76°C/50mmHg
• Molecular Weight: 264.090 g/mol
• XLogP3: 3.000
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 10
• Rotatable Bond Count: 4
• Exact Mass: 264.02 Da
• Monoisotopic Mass: 264.02 Da
• Topological Polar Surface Area: 20.200 Ų
• Heavy Atom Count: 16
• Formal Charge: 0
• Complexity: 243.000
• 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

References

1. Juan Li, Boqiang Li, Huimei Pan, Yiya Wei, Yang Yang, Nan Xu, Baiyang Chen, Madjid Mohseni, Ehsan Banayan Esfahani.  (2022)  Total organic fluorine (TOF) analysis by completely converting TOF into fluoride with vacuum ultraviolet.  JOURNAL OF HAZARDOUS MATERIALS,      [PMID:35236042] [10.1016/j.jhazmat.2022.128389]

2. Yutang Zhou, Yichao Shen, Liangjie Shi, Yong Jin, Shuangquan Lai, Yujia Tang.  (2021)  Synthesis, characterization and properties of novel nonionic hydrocarbon/fluorocarbon hybrid surfactants containing a short fluoroalkyl chain.  JOURNAL OF DISPERSION SCIENCE AND TECHNOLOGY,      [PMID:] [10.1080/01932691.2021.1930032]

3. Yichao Shen, Yong Jin, Shuangquan Lai, Liangjie Shi, Weining Du, Rong Zhou.  (2019)  Synthesis, surface properties and cytotoxicity evaluation of nonionic urethane fluorinated surfactants with double short fluoroalkyl chains.  JOURNAL OF MOLECULAR LIQUIDS,      [PMID:] [10.1016/j.molliq.2019.111851]

4. Ping Wang, Xinchao Li, Jianfeng Li, Jin Zhang, Ting Wang, Zhicheng Fu, Wenli An, Guoxing Sun, Mingjun Chen, Jinni Deng.  (2024)  Rigid polyurethane foam with durable hydrophobicity and flame retardancy endowed by novel functional surfactants.  CONSTRUCTION AND BUILDING MATERIALS,      [PMID:] [10.1016/j.conbuildmat.2024.138815]

5. Songbo Xie, Xiufen Liao, Yanye Fan, Jiacheng Li, Qiumei Jiang, Yihua Zheng, Zhimin Huang, Shella Li.  (2025)  Fluoro-Silicon-Modified Polythiourethane Copolymer for Marine Antifouling Coatings.  Coatings,  15  (5): (588).  [PMID:] [10.3390/coatings15050588]

6. Min Chen, Zhiwei Liang, Mengyuan Sun, Zhen Chen, Chun Peng, Suliman Khan, Mubbashar Abbas, Dongmei Chen, Shuyu Xie.  (2025)  Aryl hydrocarbon receptor-induced activation of AIM2 inflammasome is mediated by MOMP and MPT: A vital therapeutic pathway for inflammation.  Cell Reports,  44  (12):   [PMID:41385364] [10.1016/j.celrep.2025.116673]

7. Yajing Zhu, Anyang Duan, Zhonglin Xiang, Xiaoyan Wang, Yang Jiang, Changhai Xu, Jinmei Du.  (2026)  Fabrication of amphiphobic fabrics with excellent and durable hydrophobicity and oleophobicity via C4 short-fluorinated polymers.  POLYMER,      [PMID:] [10.1016/j.polymer.2026.129725]

8. Jianfeng Li, Ping Wang, Jin Zhang, Jiajia Jiang, Shujun Li, Wenjing Xiang, Mingjun Chen, Shuang Xia, Guoxing Sun, Zhicheng Fu, Ting Wang, Wenli An, Jinni Deng.  (2026)  Flexible Polyurethane Foam with Durable Flame Retardancy and Mechanical Properties Based on Stable Hydrophobic Protection and Cross-Linking.  ACS Applied Polymer Materials,      [PMID:] [10.1021/acsapm.5c04589]