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6-(Perfluorohexyl)hexanol is a fluorinated alcohol compound characterized by a molecular formula of C12H11F13O. It features a six-carbon chain with each carbon atom bonded to a fluorine group, along with a hydroxyl group. This colorless, odorless liquid is distinguished by its high boiling point and unique surfactant properties due to its fluorinated structure. These characteristics make it a versatile substance for a range of industrial applications, although its environmental persistence and potential risks must be considered.

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  • 161981-35-7 Structure
  • Basic information

    1. Product Name: 6-(PERFLUOROHEXYL)HEXANOL
    2. Synonyms: 6-(PERFLUOROHEXYL)HEXANOL
    3. CAS NO:161981-35-7
    4. Molecular Formula: C12H13F13O
    5. Molecular Weight: 420.21
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 161981-35-7.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 235.2°Cat760mmHg
    3. Flash Point: 96°C
    4. Appearance: /
    5. Density: 1,493 g/cm3
    6. Vapor Pressure: 0.00928mmHg at 25°C
    7. Refractive Index: 1.353
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 6-(PERFLUOROHEXYL)HEXANOL(CAS DataBase Reference)
    11. NIST Chemistry Reference: 6-(PERFLUOROHEXYL)HEXANOL(161981-35-7)
    12. EPA Substance Registry System: 6-(PERFLUOROHEXYL)HEXANOL(161981-35-7)
  • Safety Data

    1. Hazard Codes: F
    2. Statements: 36/37/38
    3. Safety Statements: 26-36/37/39
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 161981-35-7(Hazardous Substances Data)

161981-35-7 Usage

Uses

Used in Surfactant Production:
6-(Perfluorohexyl)hexanol is used as a wetting agent and lubricant in various industrial processes due to its surfactant properties. Its ability to reduce surface tension makes it effective in facilitating the spreading of liquids on surfaces and improving the flow of materials.
Used in Defoaming Agents:
6-(PERFLUOROHEXYL)HEXANOL is utilized as a component in defoaming agents, where its surfactant nature helps in controlling and reducing the formation of foam in industrial processes, which is crucial for maintaining the efficiency of certain manufacturing operations.
Used in Fluorosurfactant Production:
6-(Perfluorohexyl)hexanol is employed in the production of fluorosurfactants, which are specialty chemicals with a wide range of applications, including in the formulation of firefighting foams, coatings, and cleaning agents.
Used in Specialty Chemicals Synthesis:
Due to its unique fluorinated structure, 6-(Perfluorohexyl)hexanol has potential applications in the synthesis of other specialty chemicals, where its properties can be leveraged to create new compounds with specific functionalities.
Used in Environmental Considerations:
While 6-(Perfluorohexyl)hexanol offers numerous industrial applications, it is also recognized as a persistent pollutant. This necessitates careful management and disposal to mitigate its potential environmental impact, including risks to ecosystems and human health.

Check Digit Verification of cas no

The CAS Registry Mumber 161981-35-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,1,9,8 and 1 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 161981-35:
(8*1)+(7*6)+(6*1)+(5*9)+(4*8)+(3*1)+(2*3)+(1*5)=147
147 % 10 = 7
So 161981-35-7 is a valid CAS Registry Number.
InChI:InChI=1/C12H13F13O/c13-7(14,5-3-1-2-4-6-26)8(15,16)9(17,18)10(19,20)11(21,22)12(23,24)25/h26H,1-6H2

161981-35-7Relevant articles and documents

COMPOUNDS USEFUL IN HIV THERAPY

-

Page/Page column 159-160, (2021/10/02)

The invention relates to compounds of Formula (I), salts thereof, pharmaceutical compositions thereof, as well as methods of treating or preventing HIV in subjects.

Metal-Free Visible Light Hydroperfluoroalkylation of Unactivated Alkenes Using Perfluoroalkyl Bromides

Yajima, Tomoko,Shigenaga, Satsuki

supporting information, p. 138 - 141 (2019/01/11)

Organic dye-catalyzed visible light induced hydroperfluoroalkylation of unactivated alkenes is described. Hydroperfluoroalkylation proceeds selectively and is applicable for various perfluoroalkyl bromide and alkenes including internal alkenes. The reaction mechanism is discussed, and it is shown that the hydrogen source varies with reaction conditions.

Synthese d'acides ω perfluoroalkylalcanoiques et d'ω perfluoroalkylalcanols

Tra Anh,Blancou,Commeyras

, p. 167 - 174 (2007/10/03)

The simple and effective syntheses of acids and alcohols of general formula CnF2n+1(CH2)mY (Y=CO2H, CH2OH; n=6,8 and m=4,5) have been described.

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