Cas no 2003-04-5 (1-Propanol, 2,2,3,3,3-pentafluoro-, triester with boric acid (H3BO3))

The compound 1-Propanol, 2,2,3,3,3-pentafluoro-, triester with boric acid (H3BO3) is a fluorinated boron-containing ester with unique physicochemical properties. Its structure combines the hydrophobic and oleophobic characteristics of pentafluoropropanol with the Lewis acidity of boron, making it suitable for specialized applications. The presence of fluorine enhances thermal and chemical stability, while the boron center offers potential reactivity in cross-coupling or catalytic processes. This ester may exhibit low surface energy, suggesting utility as a surfactant or coating additive. Further investigation is warranted to explore its solubility, reactivity, and compatibility with other materials for industrial or research applications.
1-Propanol, 2,2,3,3,3-pentafluoro-, triester with boric acid (H3BO3) structure
2003-04-5 structure
Product Name:1-Propanol, 2,2,3,3,3-pentafluoro-, triester with boric acid (H3BO3)
CAS No:2003-04-5
MF:C9H6BF15O3
MW:457.92919588089
CID:4633364
Update Time:2025-11-02

1-Propanol, 2,2,3,3,3-pentafluoro-, triester with boric acid (H3BO3) Chemical and Physical Properties

Names and Identifiers

    • Tris(2,2,3,3,3-pentafluoropropyl)borate
    • 1-Propanol, 2,2,3,3,3-pentafluoro-, triester with boric acid (H3BO3) (8CI,9CI)
    • 1-Propanol, 2,2,3,3,3-pentafluoro-, triester with boric acid (H3BO3)
    • Inchi: 1S/C9H6BF15O3/c11-4(12,7(17,18)19)1-26-10(27-2-5(13,14)8(20,21)22)28-3-6(15,16)9(23,24)25/h1-3H2
    • InChI Key: MHUUWQSRUNMMHR-UHFFFAOYSA-N
    • SMILES: B(OCC(F)(F)C(F)(F)F)(OCC(F)(F)C(F)(F)F)OCC(F)(F)C(F)(F)F

1-Propanol, 2,2,3,3,3-pentafluoro-, triester with boric acid (H3BO3) Pricemore >>

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Additional information on 1-Propanol, 2,2,3,3,3-pentafluoro-, triester with boric acid (H3BO3)

Comprehensive Guide to 1-Propanol, 2,2,3,3,3-pentafluoro-, triester with boric acid (H3BO3) (CAS No. 2003-04-5)

1-Propanol, 2,2,3,3,3-pentafluoro-, triester with boric acid (H3BO3) is a specialized fluorinated boron ester compound with the CAS number 2003-04-5. This unique chemical has garnered attention in industrial and research applications due to its distinct molecular structure and versatile properties. As sustainability and advanced material innovation dominate global discussions, understanding the role of fluorinated compounds like this one becomes increasingly relevant.

The molecular structure of 1-Propanol, 2,2,3,3,3-pentafluoro-, triester with boric acid combines a pentafluoropropanol moiety with boric acid, resulting in a compound that exhibits both hydrophobic and thermal stability characteristics. These properties make it valuable in applications requiring resistance to extreme conditions, such as high-performance lubricants and specialty coatings. Researchers are particularly interested in how such fluorinated boron esters can contribute to energy-efficient solutions in manufacturing.

One of the most searched questions regarding CAS 2003-04-5 relates to its environmental impact. While fluorinated compounds often raise concerns about persistence, the esterification with boric acid in this case may offer improved biodegradability profiles compared to perfluorinated alternatives. Current studies focus on optimizing synthesis methods to reduce byproducts while maintaining the compound's performance benefits - a key consideration for industries seeking greener chemical alternatives.

In material science applications, 1-Propanol, 2,2,3,3,3-pentafluoro-, triester with boric acid demonstrates remarkable compatibility with various polymers. Its ability to modify surface properties makes it particularly useful in creating water-repellent coatings for electronic components, addressing the growing demand for moisture protection in miniaturized devices. The compound's thermal stability also positions it as a candidate for high-temperature adhesives in aerospace applications.

The synthesis of CAS 2003-04-5 typically involves the controlled esterification of pentafluoropropanol with boric acid under specific conditions. Process optimization remains an active area of research, with recent advancements focusing on catalyst selection and reaction kinetics to improve yield and purity. These developments align with the broader industry trend toward precision chemistry and controlled molecular architectures.

From a commercial perspective, the market for fluorinated boron esters like 1-Propanol, 2,2,3,3,3-pentafluoro-, triester with boric acid shows steady growth, particularly in Asia-Pacific regions where electronics manufacturing thrives. Suppliers emphasize batch-to-batch consistency and technical support as key differentiators, responding to quality-conscious buyers in specialty chemical markets.

Safety considerations for handling CAS 2003-04-5 follow standard laboratory protocols for organofluorine compounds. While not classified as hazardous under most regulatory frameworks, proper ventilation and personal protective equipment are recommended during use. Material safety data sheets provide detailed guidance specific to this chemical's physical and chemical properties.

Emerging research explores the potential of 1-Propanol, 2,2,3,3,3-pentafluoro-, triester with boric acid in energy storage applications. Preliminary studies suggest possible utility as an electrolyte additive in lithium-ion batteries, where its unique properties might enhance thermal stability - a crucial factor in next-generation battery development addressing electric vehicle needs.

Analytical characterization of CAS 2003-04-5 typically employs techniques such as NMR spectroscopy, mass spectrometry, and thermal analysis. These methods verify molecular structure and purity, ensuring the compound meets specification requirements for various applications. Quality control protocols have become increasingly stringent as end-use applications demand higher performance standards.

The future development of 1-Propanol, 2,2,3,3,3-pentafluoro-, triester with boric acid derivatives appears promising, with research focusing on modified versions that retain beneficial properties while offering improved environmental profiles. Such innovations could expand the compound's applicability in sustainable technologies and circular economy initiatives gaining traction worldwide.

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