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3,3,4,4,5,5,6,6,6-Nonafluoro-1-hexanol acetate is a fluorinated alcohol derivative that is frequently used as a solvent and a surfactant. It is known for its unique chemical structure, low surface tension, and excellent repellent properties, making it ideal for use in various industrial applications.

80705-15-3

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80705-15-3 Usage

Uses

Used in Coatings Industry:
3,3,4,4,5,5,6,6,6-Nonafluoro-1-hexanol acetate is used as a solvent and surfactant for the production of high-performance coatings. Its low surface tension and excellent repellent properties make it useful in water and oil repellent coatings, providing enhanced durability and stability.
Used in Adhesives Industry:
3,3,4,4,5,5,6,6,6-Nonafluoro-1-hexanol acetate is used as a component in the formulation of adhesives, contributing to their high performance and stability. Its unique chemical structure allows for improved bonding and adhesion properties.
Used in Lubricants Industry:
3,3,4,4,5,5,6,6,6-Nonafluoro-1-hexanol acetate is used in the manufacturing of lubricants, where its low surface tension and excellent repellent properties contribute to reduced friction and wear, enhancing the overall performance and longevity of the lubricants.

Check Digit Verification of cas no

The CAS Registry Mumber 80705-15-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,7,0 and 5 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 80705-15:
(7*8)+(6*0)+(5*7)+(4*0)+(3*5)+(2*1)+(1*5)=113
113 % 10 = 3
So 80705-15-3 is a valid CAS Registry Number.

80705-15-3Downstream Products

80705-15-3Relevant academic research and scientific papers

Synthesis of fluoroalkyl ethanal: R(F)CH2CHO

Laurent,Blancou,Commeyras

, p. 2489 - 2492 (2007/10/02)

Aldehydes R(F)CH2CHO (R(F) is a linear perfluoroalkyl chain) have been obtained in the addition reaction of R(F)I to vinyl acetate in the presence of zinc. R(F)CH2CHIOAc is formed as an intermediate in the course of the reaction. Under appropriate conditions, R(F)CH2CHO and its acylal or acetal derivatives are obtained in good yields.

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