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Specifications of 2,2-Difluoroethanol丨CAS 359-13-7
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Appearance: |
Colorless liquid |
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Assay: |
99.0% min |
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Methanol: |
0.3% max |
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Moisture: |
0.3% max |
Transport Information of 2,2-Difluoroethanol丨CAS 359-13-7
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Parameter |
Specification |
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UN Number |
1987 |
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Class |
3 |
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Packing Group |
II |
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H.S. Code |
2905590090304 |
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Stability & Reactivity |
The product is chemically stable under standard ambient conditions (room temperature). |
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Storage |
Tightly closed. Store in a closed, dry, ventilated place |
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Condition to Avoid |
Avoid excessive heat and light. |
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Package |
Manufacturing Information of 2,2-Difluoroethanol丨CAS 359-13-7
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Parameter |
Specification |
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Capacity |
5MT/month |
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Frequency |
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Main Export Countries |
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Capacity/Batch |
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Experience |
Production since 2014 |
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Stock |
Applications of 2,2-Difluoroethanol丨CAS 359-13-7
1. Intermediate in Organic Synthesis
●Fluorinated Building Block: 2,2-Difluoroethanol丨CAS 359-13-7 serves as a key intermediate in organic synthesis, particularly for introducing fluorine atoms into molecules. The presence of fluorine can significantly alter the biological activity, lipophilicity, and metabolic stability of compounds.
●Synthesis of Ethers and Esters: It is used to synthesize difluoroethyl ethers and esters, important intermediates in medicinal chemistry and agrochemical development.
2. Pharmaceutical Research
●Fluorinated Drug Design: Fluorine-containing molecules are crucial in modern drug discovery due to fluorine's ability to enhance binding affinity, bioavailability, and metabolic resistance. 2,2-Difluoroethanol is often incorporated into drug candidates to improve these properties.
●Prodrug Strategies: It may be used as a pro-moiety in the design of prodrugs, helping improve solubility or controlled release characteristics.
3. Agrochemical Industry
●Pesticide Intermediate: Used in the synthesis of fluorinated pesticides and herbicides. The introduction of difluoroethyl groups can improve the efficacy, soil stability, and systemic behavior of crop protection agents.
4. Material Science
●Polymer Chemistry: 2,2-Difluoroethanol can be used to introduce fluorinated side chains into polymer backbones, improving their chemical resistance, hydrophobicity, and thermal stability.
●Functionalized Coatings: Used in surface coatings to impart anti-stick, low-surface energy, or water-repellent properties.
5. Radiolabeling and Fluorinated Compounds
●Precursors in Radiopharmaceuticals: As a fluorinated alcohol, it serves as a structural analog or synthetic precursor to molecules labeled with radioactive fluorine isotopes, such as ¹⁸F, used in PET imaging.
●Fine Chemical Synthesis: Useful in the creation of fine chemicals with high electron-withdrawing substituents for use in electronics and advanced materials.
Benefits of 2,2-Difluoroethanol丨CAS 359-13-7
1. Fluorine Functionality
●The difluoroethyl group is a valuable pharmacophore and substituent that provides molecules with enhanced chemical and biological properties-often increasing membrane permeability and enzyme resistance.
2. Improved Pharmacokinetics
●Molecules derived from or containing 2,2-difluoroethanol often demonstrate longer biological half-lives and better metabolic profiles, which is desirable in drug development.
3. Compact and Reactive
●As a small, low molecular weight compound with a reactive hydroxyl group, it's easy to incorporate into a wide range of chemical reactions, allowing for versatile downstream derivatization.
4. Stability and Solubility
●Offers good chemical stability and is soluble in both water and organic solvents, making it suitable for use in varied synthetic environments.
Conclusion
2,2-Difluoroethanol丨CAS 359-13-7 is a valuable, versatile fluorinated alcohol used across pharmaceutical, agrochemical, and materials science sectors. Its ability to introduce difluoroethyl groups enhances the biological activity, durability, and chemical stability of final products. Whether used as a building block for drug discovery, a modifier in functional materials, or a precursor in advanced chemical synthesis, it plays a critical role in the development of next-generation compounds with enhanced properties.

