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1H,1H,2H,3H,3H-Perfluorononane-1,2-diol is a complex organic compound with a fully fluorinated long carbon chain and two hydroxyl groups at one end. Its unique molecular structure provides high stability and resistance to harsh conditions, making it suitable for various industrial applications.

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  • 107650-06-6 Structure
  • Basic information

    1. Product Name: 1H,1H,2H,3H,3H-PERFLUORONONANE-1,2-DIOL
    2. Synonyms: 1H,1H,2H,2H-PERFLUORONONANE-1,2-DIOL;1H,1H,2H,3H,3H-PERFLUORONONANE-1,2-DIOL;Perfluorononanediol;1H,1H,2H,3H,3H-Perfluorononane-1,2-diol 97%;1H,1H,2H,3H,3H-Perfluorononane-1,2-diol97%;4,4,5,5,6,6,7,7,8,8,9,9,9-Tridecafluorononane-1,2-diol;4,4,5,5,6,6,7,7,8,8,9,9,9-Tridecafluorononane-1,2-diol 97%;4,4,5,5,6,6,7,7,8,8,9,9,9-Tridecafluorononane-1,2-diol97%
    3. CAS NO:107650-06-6
    4. Molecular Formula: C9H7F13O2
    5. Molecular Weight: 394.13
    6. EINECS: -0
    7. Product Categories: N/A
    8. Mol File: 107650-06-6.mol
  • Chemical Properties

    1. Melting Point: 63-64°C
    2. Boiling Point: 120-130°C
    3. Flash Point: >150°C
    4. Appearance: /
    5. Density: 1.617g/cm3
    6. Vapor Pressure: 0.0432mmHg at 25°C
    7. Refractive Index: 1.322
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. PKA: 13.52±0.20(Predicted)
    11. CAS DataBase Reference: 1H,1H,2H,3H,3H-PERFLUORONONANE-1,2-DIOL(CAS DataBase Reference)
    12. NIST Chemistry Reference: 1H,1H,2H,3H,3H-PERFLUORONONANE-1,2-DIOL(107650-06-6)
    13. EPA Substance Registry System: 1H,1H,2H,3H,3H-PERFLUORONONANE-1,2-DIOL(107650-06-6)
  • Safety Data

    1. Hazard Codes: Xi
    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: 107650-06-6(Hazardous Substances Data)

107650-06-6 Usage

Uses

Used in Lubricants:
1H,1H,2H,3H,3H-Perfluorononane-1,2-diol is used as a lubricant ingredient for its extreme thermal and chemical stability, which is essential in applications requiring high performance under challenging conditions.
Used in Surfactants:
1H,1H,2H,3H,3H-Perfluorononane-1,2-diol is used as a surfactant component due to its ability to lower surface tension and improve the spreading and wetting properties of various products, enhancing their performance.
Used in Industrial Applications:
1H,1H,2H,3H,3H-Perfluorononane-1,2-diol is used as a key ingredient in various industrial products that require high stability and resistance to extreme conditions, such as in the manufacturing of coatings, adhesives, and other specialized materials.
However, it is important to note that the use of perfluorinated compounds has been under increased scrutiny due to their potential environmental and health impacts. As a result, there may be limitations or regulations on their application in certain industries.

Check Digit Verification of cas no

The CAS Registry Mumber 107650-06-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,7,6,5 and 0 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 107650-06:
(8*1)+(7*0)+(6*7)+(5*6)+(4*5)+(3*0)+(2*0)+(1*6)=106
106 % 10 = 6
So 107650-06-6 is a valid CAS Registry Number.
InChI:InChI=1/C9H7F13O2/c10-4(11,1-3(24)2-23)5(12,13)6(14,15)7(16,17)8(18,19)9(20,21)22/h3,23-24H,1-2H2

107650-06-6 Well-known Company Product Price

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  • Alfa Aesar

  • (L16598)  1H,1H,2H,3H,3H-Perfluorononane-1,2-diol, 95%   

  • 107650-06-6

  • 5g

  • 769.0CNY

  • Detail
  • Alfa Aesar

  • (L16598)  1H,1H,2H,3H,3H-Perfluorononane-1,2-diol, 95%   

  • 107650-06-6

  • 25g

  • 2612.0CNY

  • Detail

107650-06-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1H,1H,2H,3H,3H-PERFLUORONONANE-1,2-DIOL

1.2 Other means of identification

Product number -
Other names 4,4,5,5,6,6,7,7,8,8,9,9,9-tridecafluorononane-1,2-diol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:107650-06-6 SDS

107650-06-6Relevant articles and documents

Synthesis and characterization of perfluorohexylated poly(3,4-ethylenedioxythiophene)

Zuo, Liangbin,Qing, Feng-Ling,Meng, Wei-Dong,Huang, Xiaoyu,Zhang, Sen,Wu, Qiang

, p. 1441 - 1446 (2007/10/03)

The perfluorohexylated 3,4-ethylenedioxythiophene 5 was prepared via Mitsunobu reaction of perfluorohexylatyed diol 2 with diethyl 3,4-dihydroxythiophenedicarboxylate followed by decarboxylation. The polymerization of 5 was conducted with both oxidative chemical and electrochemical polymerizations. The polymers were characterized by cyclic voltammogram, UV, IR, TGA and DSC.

Chemistry of [(perfluoroalkyl)methyl] oxiranes. Regioselectivity of ring opening with O-nucleophiles and the preparation of amphiphilic monomers

Cirkva, Vladimir,Ameduri, Bruno,Boutevin, Bernard,Paleta, Oldrich

, p. 53 - 61 (2007/10/03)

The reactions of oxiranes RFCH2CH(-O-)CH2 (RF≡C4F9, C6F13, C8F17; 4a-4c) with a series of alkanols in the presence of a Lewis acid took place at the terminal carbon atom with complete regioselectivity. 2-Hydroxyethyl methacrylate and acrylate reacted similarly. The reaction with alkane diols was controlled to proceed with one or two molecules of the oxiranes chemoselectively. Non-regioselective, base-catalysed ring opening by methacrylic acid (83% terminal attack) was discussed on the basis of the hard and soft acids and bases (HSAB) concept. A convenient transformation of the oxiranes to the corresponding diols 13a-13c via dioxolane intermediates, and their conversion to bis-methacrylates, was accomplished with overall yields of 75%-79%. Thiourea converted the oxiranes into the corresponding thiiranes (15a-15c). The reactions afforded products generally in yields of 82%-98%.

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