비닐 플루오르화물
비닐플루오라이드 · 비닐플루오르화물 · 플루오린화바이닐(플루오르화비닐) · 비닐 플루오라이드 · Ethene, fluoro- · FLUOROETHYLENE · Fluoroethene · C2H3F

식별자 및 물리적 특성
| CAS No. | 75-02-5 |
|---|---|
| 분자식 | C2H3F |
| 평균 분자량 | 46.04 g/mol |
| 단동위원소 질량 | 46.02187826 g/mol |
| SMILES | C=CF |
| InChIKey | XUCNUKMRBVNAPB-UHFFFAOYSA-N |
| PubChem CID | 6339 |
| ChEBI | CHEBI:51314 |
| EC No. | 200-832-6 |
| DTXSID | DTXSID3021435 |
| 현지명 | 비닐 플루오르화물 |
화학 및 물리적 성질
| XLogP | 1 |
|---|---|
| 극성 표면적 | 0 |
| 수소 결합 공여자 수 | 0 |
| 수소 결합 수용자 수 | 1 |
| 회전 가능 결합 수 | 0 |
| 무거운 원자 수 | 3 |
| 형식 전하 | 0 |
| 복잡도 | 10 |
| LogP(분배 계수) | log Kow = 1.19 /Estimated/ |
| 냄새 | Faint, ethereal odor. |
| 밀도 | 0.707 at 32 °F (USCG, 1999) - Less dense than waterwill float0.636 (liquid) at 21 °CHeat of evaporation: 13494 J/mol at -20 °CDensity = 0.775 g/cu cm at -30 °CCritical density = 0.320 g/cu cm0.636 @ 21°C (Liquid)1.60(relative gas density)0,615 g/cm3 |
| Viscosity | 3.2347E-04 pascal/seconds (liquid) @ boiling point |
| Color/Form | Colorless gas [Note: Shipped as a liquefied compressed gas]. |
| 용해도 | Insoluble (NIOSH, 2024)Soluble in ether.Soluble in ethanol and acetoneWater solubility at 80 °C (g/100 g water): 0.94 (at 3.4 MPa), 1.54 (at 6.9 MPa)In water, 1.29X10+4 mg/L at 25 °C /Estimated/Solubility in water: none |
| 인화점 | Flammable gasNA (Gas) |
| 끓는 점 | -98 °F at 760 mmHg (USCG, 1999)-72 °C-72 °C @760 [mm Hg]-72°C |
| Decomposition | When heated to decomposition it emits toxic fumes of /hydrogen fluoride/. |
| 녹는점 | -258 °F (USCG, 1999)-160.5 °C-161 °C-257 °F-160,5°C |
| 증기 밀도 | 1.6 (NIOSH, 2024) - Heavier than airwill sink (Relative to Air)1.58 (Air= 1)Relative vapor density (air = 1): 1.6 |
| Polymerization | In the absence of inhibitor, polymerization can occurPolymerizes freely |
| 굴절률 | 1.34 |
| 헨리 상수 | 8.2×10-5 mol/(m3Pa) at 25℃, HSDB (2015) |
| EPA | Vinyl fluoride (75-02-5) |
화학적 성질
Vinyl fluoride is a colorless gas.
안전 및 규제
| GHS 분류 | DangerH220 (100%): Extremely flammable gas [Danger Flammable gases]H280 (100%): Contains gas under pressuremay explode if heated [Warning Gases under pressure]H341 (45.6%): Suspected of causing genetic defects [Warning Germ cell mutagenicity]H350 (45.6%): May cause cancer [Danger Carcinogenicity]H373 (45.6%): May causes damage to organs through prolonged or repeated exposure [Warning Specific target organ toxicity, repeated exposure]P203, P210, P222, P260, P280, P318, P319, P377, P381, P403, P405, P410+P403, and P501 (click each P-code to see the statement)Aggregated GHS information provided per 114 reports by companies from 4 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.Information may vary between notifications depending on impurities, additives, and other factors. The percentage value in parenthesis indicates the notified classification ratio from companies that provide hazard codes. Only hazard codes with percentage values above 10% are shown. For more detailed information, please visit ECHA C&L website. |
|---|---|
| 규제 정보 | Chemical: Ethene, fluoro-Hazard Traits - CarcinogenicityAuthoritative List - IARC Carcinogens - 2ANTP RoC - reasonableProp 65Report - regardless of intended function of ingredient in the productEthene, fluoro- is listed on the EPA's Chemical Data Reporting (CDR) system. Manufacturers and importers of Ethene, fluoro- are required to report information about their production and use of this chemical to the EPA under the Toxic Substances Control Act (TSCA). (40 eCFR Part 711)Status: Active Update: 30-01-2014 https://echa.europa.eu/registration-dossier/-/registered-dossier/10395The New Jersey Worker and Community Right to Know Act requires public and private employers to provide information about hazardous substances at their workplaces. (N.J.S.A. 34:5A-1 et. seq.) |
| 기타 안전 정보 | IMAP assessments - Ethene, fluoro-: Human health tier II assessmentIMAP assessments - Ethene, fluoro-: Environment tier I assessment |
| 운송 라벨(DOT) | Flammable Gas |
| 화재 위험 | Special Hazards of Combustion Products: Toxic hydrogen fluoride gas is generated in a fire. |
용도
개요
Vinyl fluoride (VF) was first synthesized by Frederic Swarts, a Belgian chemist in 1901, by the reaction between zinc and 1,1-difluoro-2-bromoethane. Modern preparation involves the reaction of acetylene and hydrogen fluoride (HF) in the presence of a mercury- or aluminum-based catalyst. The US Environmental Protection Agency (EPA) listed VF as a highproduction- volume chemical in 1990. According to National Toxicology Program (NTP), 2005, the annual production of VF in the United States was above 1 million pounds (454 000 kg) in 1990 and approximately 3.3 million pounds (1.5 million kg) in 2001.
용도
Vinyl fluoride is used primarily in the production of polyvinyl fluoride and other fluoropolymers. Polymers of vinyl fluoride are resistant to weather and exhibit great strength, chemical inertness, and low permeability to air and water. Polyvinyl fluoride is laminated with aluminum, galvanized steel, and cellulose materials and is used as a protective surface for the exteriors of residential and commercial buildings. Polyvinyl fluoride laminated with various plastics has been used to cover walls, pipes, and electrical equipment and inside aircraft cabins (IARC 1995).
일반 설명
A colorless gas with a faint ethereal odor. Shipped as a confined liquid under its vapor pressure. Any leak can either be liquid or vapor. Contact with the liquid can cause frostbite. Easily ignited. Vapors are heavier than air. Can asphyxiate by the displacement of air. Under prolonged exposure to fire or intense heat the containers may rupture violently and rocket.
제조 및 합성 방법
생산 방법
The first preparation of VF in the early 1900s was by reacting zinc with 1,1-difluoro-2-bromomethane. VF was considered to be a high production volume chemical according to the U.S. Environmental Protection Agency with annual production exceeding 1million lb in 1990. In 2001, annual U.S. production was estimated approximately 3.3 million lb. In 1994, VF was produced by one company each in Japan and the United States. More recently, only one U.S. manufacturer of VF was identified . Information on European manufacturer is not available. The modern production is by the addition of hydrogen fluoride to acetylene over a mercury- or aluminum-based catalyst.
제조 방법
Vinyl fluoride may be obtained from acetylene by either of the two following routes:In the first method, acetylene is heated with hydrogen fluoride in the presence of a catalyst of mercuric chloride on charcoal at about 40C to yield vinyl fluoride directly. In the second method, acetylene is treated with an excess of hydrogen fluoride to form difluoroethane which is then pyrolysed at about 700C in a platinum tube to give vinyl fluoride, which is separated by distillation under pressure.Vinylidene fluoride is obtained from vinylidene chloride by the following route:In the first stage, vinylidene chloride undergoes addition with hydrogen chloride at about 30C and atmospheric pressure in the presence of a FriedelCrafts type catalyst. The resulting trichloroethane is then treated with hydrogen fluoride at about 180C and 3 MPa (30 atmospheres) in the presence of antimony pentachloride to give chlorodifluoroethane. Pyrolysis of this product yields vinylidene fluoride. Vinylidene fluoride is a gas, b.p. -84C.