
H-substitued ,ether-substituted perfluoroalkyl (linear)sulfonic acids (HOPFLSA n=5) (CHEM103933)
| Record Information | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| Version | 1.0 | ||||||||
| Creation Date | 2026-04-05 14:51:00 UTC | ||||||||
| Update Date | 2026-09-01 11:16:45 UTC | ||||||||
| Accession Number | CHEM103933 | ||||||||
| Identification | |||||||||
| Common Name | H-substitued ,ether-substituted perfluoroalkyl (linear)sulfonic acids (HOPFLSA n=5) | ||||||||
| Class | Small Molecule | ||||||||
| Description | H-substitued,ether-substituted perfluoroalkyl (linear)sulfonic acids (HOPFLSA n=5) is an organic compound with the formula C7H2F14O4S and an average molecular weight of 448.13 g/mol. H-substitued,ether-substituted perfluoroalkyl (linear)sulfonic acids (HOPFLSA n=5) belongs to the organosulfonic acids and derivatives, a subclass of organic sulfonic acids and derivatives within the organic compounds. This compound has been found in or released from 13 recorded sources across multiple sectors. These include electrical and electronic equipment, specifically batteries, capacitors, cell phones, printed circuit boards, and wires and cables. It is also associated with textiles, leather and furnishings, including carpets, rugs, and synthetic textiles. In the healthcare, pharmaceuticals and veterinary products sector, it is found in medical devices, while in the food, food processing and cookware sector, it is present in food packaging. Additionally, it is used as lubricants within the energy, oil and gas sector as well as in industrial manufacturing and chemical processing. One other sector has also been recorded. Recorded exposure routes for this substance include oral, inhalation, and touch. | ||||||||
| Contaminant Sources | Not Available | ||||||||
| Contaminant Type |
| ||||||||
| Chemical Structure | |||||||||
| Synonyms | Not Available | ||||||||
| Chemical Formula | C7H2F14O4S | ||||||||
| Average Molecular Mass | Not Available | ||||||||
| Monoisotopic Mass | 447.945 g/mol | ||||||||
| CAS Registry Number | Not Available | ||||||||
| IUPAC Name | 2-(1,1,2,2,3,3,4,4,5,5-decafluoropentoxy)-1,1,2,2-tetrafluoroethanesulfonic acid | ||||||||
| Traditional Name | Not Available | ||||||||
| SMILES | C(C(C(C(C(OC(C(F)(F)S(=O)(=O)O)(F)F)(F)F)(F)F)(F)F)(F)F)(F)F | ||||||||
| InChI Identifier | InChI=1S/C7H2F14O4S/c8-1(9)2(10,11)3(12,13)4(14,15)5(16,17)25-6(18,19)7(20,21)26(22,23)24/h1H,(H,22,23,24) | ||||||||
| InChI Key | IYAFCGZBAFKFSQ-UHFFFAOYSA-N | ||||||||
| Chemical Taxonomy | |||||||||
| Classification | Not classified | ||||||||
| Biological Properties | |||||||||
| Status | Detected and Not Quantified | ||||||||
| Origin | Not Available | ||||||||
| Cellular Locations | Not Available | ||||||||
| Biofluid Locations | Not Available | ||||||||
| Tissue Locations | Not Available | ||||||||
| Pathways | Not Available | ||||||||
| Applications | Not Available | ||||||||
| Biological Roles | Not Available | ||||||||
| Chemical Roles | Not Available | ||||||||
| Physical Properties | |||||||||
| State | Not Available | ||||||||
| Appearance | Not Available | ||||||||
| Experimental Properties |
| ||||||||
| Predicted Properties | Not Available | ||||||||
| Spectra | |||||||||
| Spectra |
| ||||||||
| Toxicity Profile | |||||||||
| Route of Exposure | Not Available | ||||||||
| Mechanism of Toxicity | Not Available | ||||||||
| Metabolism | Not Available | ||||||||
| Toxicity Values | Not Available | ||||||||
| Lethal Dose | Not Available | ||||||||
| Carcinogenicity (IARC Classification) | Not Available | ||||||||
| Uses/Sources | Not Available | ||||||||
| Minimum Risk Level | Not Available | ||||||||
| Health Effects | Not Available | ||||||||
| Symptoms | Not Available | ||||||||
| Treatment | Not Available | ||||||||
| Concentrations | |||||||||
| Not Available | |||||||||
| External Links | |||||||||
| Identifiers | Not Available | ||||||||
| References | |||||||||
| Synthesis Reference | Not Available | ||||||||
| MSDS | Not Available | ||||||||
| General References | Not Available | ||||||||