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3792-02-7

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3792-02-7 Usage

Description

5,5,6,6,7,7,8,8,8-NONAFLUOROOCTAN-1-OL, also known as C8F17OH or perfluorooctyl alcohol, is a fluorinated compound with the chemical formula C8F17OH. It is a clear, colorless, and odorless liquid that is immiscible in water and has a high boiling point. Due to its fluorinated nature, it is highly stable, inert, and resistant to heat, chemicals, and solvents, making it a valuable and versatile chemical in various industrial and manufacturing processes.

Uses

Used in Pharmaceutical Industry:
5,5,6,6,7,7,8,8,8-NONAFLUOROOCTAN-1-OL is used as a surfactant, emulsifier, and wetting agent for the formulation of pharmaceutical products. Its properties allow for improved solubility, stability, and bioavailability of drugs.
Used in Textile Industry:
In the textile industry, 5,5,6,6,7,7,8,8,8-NONAFLUOROOCTAN-1-OL is used as a surfactant and wetting agent to enhance the dyeing and finishing processes. Its ability to lower surface tension helps improve the wetting and spreading of dyes on fabric surfaces.
Used in Electronics Industry:
5,5,6,6,7,7,8,8,8-NONAFLUOROOCTAN-1-OL is used as a surfactant and wetting agent in the electronics industry for the manufacturing of printed circuit boards and other electronic components. Its stability and resistance to heat and chemicals make it suitable for use in harsh manufacturing environments.
Used as a Lubricant:
5,5,6,6,7,7,8,8,8-NONAFLUOROOCTAN-1-OL is used as a lubricant in various applications due to its low friction coefficient and resistance to wear. Its stability and inertness make it suitable for use in high-temperature and chemically aggressive environments.
Used in the Production of Fluorinated Polymers:
5,5,6,6,7,7,8,8,8-NONAFLUOROOCTAN-1-OL is used as a component in the production of fluorinated polymers, which have a wide range of applications in various industries, including aerospace, automotive, and medical.
It is important to handle 5,5,6,6,7,7,8,8,8-NONAFLUOROOCTAN-1-OL with care as it may have potential health and environmental risks.

Check Digit Verification of cas no

The CAS Registry Mumber 3792-02-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,7,9 and 2 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 3792-02:
(6*3)+(5*7)+(4*9)+(3*2)+(2*0)+(1*2)=97
97 % 10 = 7
So 3792-02-7 is a valid CAS Registry Number.
InChI:InChI=1/C8H9F9O/c9-5(10,3-1-2-4-18)6(11,12)7(13,14)8(15,16)17/h18H,1-4H2

3792-02-7Relevant articles and documents

Effect of the fluorination degree of partially fluorinated octyl-phosphocholine surfactants on their interfacial properties and interactions with purple membrane as a membrane protein model

Baba, Teruhiko,Takagi, Toshiyuki,Sumaru, Kimio,Kanamori, Toshiyuki

, (2020)

Interfacial properties and membrane protein solubilization activity of a series of partially fluorinated octyl-phosphocholine (PC) surfactants were investigated from the viewpoint of the fluorination degree of the hydrophobic chain. The critical micelle concentration (CMC), surface tension lowering activity, molecular occupied area at the CMC and free energy changes of micellization as well as adsorption to the air-water interface for each PC surfactant were estimated from surface tension measurements at 25 °C. The PCs with higher degree of fluorination exhibited low CMC and high surface activity, while the single trifluoromethyl group at the end of the chain appeared to enhance the hydrophilicity of the surfactant molecule. Under conditions where conventional short-chain surfactants, n-octyl-β-D-glucoside, Triton X-100 and dioctanoylphosphatidylcholine significantly solubilize purple membranes (PM), none of the fluorinated-PCs solubilized PM. This suggests that fluorinated-PCs are low-invasive enough to maintain the structure of lipids/protein assemblies like PM.

METHOD FOR PREPARING FLUORINATED BENZOTRIAZOLE COMPOUNDS

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Page/Page column 5, (2008/12/05)

Fluorinated benzotriazole compounds may be prepared by contacting a fluorochemical monofunctional compound, such a fluorinated alcohol, with a carboxybenzotriazole in the presence of a coupling agent, and an optional amine catalyst.

3-methyl-chroman and -thiochroman derivatives

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, (2008/06/13)

The present invention provides a compound having the following general formula (1): in which R1represents a hydrogen atom, etc.; R2represents a C3-C3perhalogenoalkyl group, etc.; each of R3and R4independently represents a hydrogen atom, etc.; X represents an oxygen atom or a sulfur atom; m represents an integer of 2 to 14; and n represents an integer of 0 to 8; or enantiomers of the compound, or hydrates or pharmaceutically acceptable salts of the compound or its enantiomers. The compound of general formula (1) is advantageous in pharmaceutical use because of its anti-estrogenic activity.

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