307-24-4
Product Name:
Perfluorohexanoic acid
Formula:
C6HF11O2
Synonyms:
Perfluorocaproic acid;Perfluorohexanoic acid
Inquiry
CHEMICAL AND PHYSICAL PROPERTIES
| Color/Form | Colorless liquid |
|---|---|
| Boiling Point | 157 °C |
| Solubility | In water, 15,700 mg/L at ambient temperature |
| Vapor Pressure | 1.49 ± 0.06 [log Psd at 298.15 K (Pa)] |
| Stability/Shelf Life | Stable under recommended storage conditions. |
| Enthalpy of Sublimation | 68.5 ± 14.0 [ΔsubHb (kJ/mol) at 269.3-284.7 K] |
| Dissociation Constants | pKa = -0.16 |
| Collision Cross Section | 125.1 Ų [M-H-CO2]- [CCS Type: DT; Buffer gas: N2; Dataset: PFAS] |
| Chemical Classes | PFAS |
SAFETY INFORMATION
| Signal word | Danger |
|---|---|
| Pictogram(s) |
 Corrosion Corrosives GHS05 |
| GHS Hazard Statements |
H314:Skin corrosion/irritation |
| Precautionary Statement Codes |
P280:Wear protective gloves/protective clothing/eye protection/face protection. P363:Wash contaminated clothing before reuse. P303+P361+P353:IF ON SKIN (or hair): Remove/Take off Immediately all contaminated clothing. Rinse SKIN with water/shower. P305+P351+P338:IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing. P405:Store locked up. |
COMPUTED DESCRIPTORS
| Molecular Weight | 314.05 g/mol |
|---|---|
| XLogP3 | 3.6 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 13 |
| Rotatable Bond Count | 4 |
| Exact Mass | 313.98008905 g/mol |
| Monoisotopic Mass | 313.98008905 g/mol |
| Topological Polar Surface Area | 37.3 Ų |
| Heavy Atom Count | 19 |
| Formal Charge | 0 |
| Complexity | 368 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently-Bonded Unit Count | 1 |
| Compound Is Canonicalized | Yes |
PRODUCT INTRODUCTION
description
Perfluorohexanoic acid is a monocarboxylic acid that is perfluorinated hexanoic acid. It has a role as an environmental contaminant and a xenobiotic. It is functionally related to a hexanoic acid.