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| Perfluorononanoic acid Basic information |
Product Name: | Perfluorononanoic acid | Synonyms: | HEPTADECAFLUORO-N-NONANOIC ACID;HEPTADECAFLUOROPELARGONIC ACID;PERFLUORONONANOIC ACID;PERFLUORO-N-NONANOIC ACID;PERFLUOROPELARGONIC ACID;N-HEPTADECAFLUORONONANOIC ACID;2,2,3,3,4,4,5,5,6,6,7,7,8,8,9,9,9-Heptadecafluorononanoic acid;heptadecafluoro-nonanoicaci | CAS: | 375-95-1 | MF: | C9HF17O2 | MW: | 464.08 | EINECS: | 206-801-3 | Product Categories: | Fluorous Chemistry;Fluorous Compounds;Synthetic Organic Chemistry | Mol File: | 375-95-1.mol | |
| Perfluorononanoic acid Chemical Properties |
Melting point | 59-62 °C (lit.) | Boiling point | 218°C | density | 1.7397 (estimate) | Fp | 218°C | storage temp. | Refrigerator | solubility | Acetone (Slightly), DMSO (Slightly), Methanol (Slightly) | pka | 0.52±0.10(Predicted) | form | Solid | color | Off-White to Beige | BRN | 1897287 | Stability: | Stable. Incompatible with strong bases, strong oxidizing agents. Corrosive - causes burns. | CAS DataBase Reference | 375-95-1(CAS DataBase Reference) | EPA Substance Registry System | Perfluorononanoic acid (375-95-1) |
| Perfluorononanoic acid Usage And Synthesis |
Chemical Properties | Perfluorononanoic acid is a white crystalline powder or beige crystals. Perfluorononanoic acid has the ability to react with bases, oxidizing agents, and reducing agents. Upon decomposition, PFNA can form carbon oxides and hydrogen fluoride. | Uses | Perfluorinated compounds (PFCs) are persistent in environments due to the high energy of C-F bond
routes. PFNA may interfere in a toxic fashion on the immune system, liver, development, and endocrine systems. | Uses | Perfluorinated compounds (PFCs) are persistent in environments due to the high energy of C-F bond. Being a persistent environmental pollutant, it can accumulate in human tissues via various exposure routes. PFNA may interfere in a toxic fashion on the immune system, liver, development, and endocrine systems. | Definition | ChEBI: A fluoroalkanoic acid that is nonanoic acid in which all of the hydrogens in the alkyl chain are replaced by fluorines. |
| Perfluorononanoic acid Preparation Products And Raw materials |
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