88645-29-8FC(F)=C(F)FBFKJFAAPBSQJPD-UHFFFAOYSA-NTetrafluoroethylene can cause cancer according to The National Toxicology Program.
88645-29-8CHEMBL541730CHEBI:38866Other Classes -> Halogenated Aliphatics, Unsaturated
Carcinogens
PFAS -> Other/unspecified
PFAS -> Suspected persistent, mobile, toxic (PMT) PFAS or PFAS-like compounds
PFAS -> Fluoropolymers
PFAS -> Other/unspecified
PFAS -> PFAS identified in REACH Regulation EC No. 1272/2008
PFAS -> Other/unspecified
1.519 at -105 °F (NTP, 1992) - Denser than water; will sink
1.519 g/cu cm at -76 °C
Critical density = 0.58 g/cu cm; Heat of evaporation = 16,821 J/mol at -75.6 °C
Density (at -76 °C): 1.5 g/cm³
1.519 at -105 °F
1.519 @ -76°C
Sicherheitsangaben dienen nur zur Orientierung und ersetzen weder das Sicherheitsdatenblatt (SDB) des Lieferanten noch geltende Vorschriften oder eine fachliche Bewertung.
Danger
H350: May cause cancer [Danger Carcinogenicity]
P203, P280, P318, P405, and P501 (click each P-code to see the statement)
This chemical does not meet GHS hazard criteria for 59.3% (481 of 811) of all reports.
Danger
H220 (30.7%): Extremely flammable gas [Danger Flammable gases]
Chemical: Ethene, tetrafluoro-
Hazard Traits - Carcinogenicity
Ethene, 1,1,2,2-tetrafluoro- is listed on the EPA's Chemical Data Reporting (CDR) system. Manufacturers and importers of Ethene, 1,1,2,2-tetrafluoro- 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: 24-04-2023 https://echa.europa.eu/registration-dossier/-/registered-dossier/15453
Tetrafluoroethylene: Does not have an individual approval but may be used as a component in a product covered by a group standard. It is not approved for use as a chemical in its own right.
The 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.)
Special Hazards of Combustion Products: When burned in air, gas forms toxic carbonyl fluoride and hydrogen fluoride.
· EXTREMELY FLAMMABLE.
Highly flammable. Cylinder may explode in heat of fire. Gives off irritating or toxic fumes (or gases) in a fire. Risk of fire and explosion on contact with air. See Chemical Dangers. Gas/air mixtures are explosive.
S-(1,1,2,2-Tetrafluoroethyl)-L-cysteine (TFEC), a major metabolite of the industrial gas tetrafluoroethylene, has been shown to mediate nephrotoxicity by necrosis. TFEC-induced cell death is associated with an early covalent modification of specific intramitochondrial proteins; including aconitase, alpha-ketoglutarate dehydrogenase (KGDH) subunits, HSP60 and HSP70. Previous studies have indicated that the TAMH line accurately models TFEC-induced in vivo cell death with dose- and time-dependent inhibitions of both KGDH and aconitase activities. Here, ... the molecular pathway leading to TFEC-mediated cell death /was shown to be/ associated with an early cytosolic to mitochondrial translocation of BAX, a pro-apoptotic member of the BCL-2 family. Immunoblot analyses indicated movement of BAX (21 kDa) to the mitochondrial fraction after exposure to a cytotoxic concentration of TFEC (250 uM). Subsequent cytochrome c release from mitochondria was also demonstrated, but only a modest increase in caspase activities was observed, suggesting a degeneration of early apoptotic signals into secondary necrosis. Significantly, TAMH cells overexpressing BCL-xL preserved cell viability even to supratoxicological concentrations of TFEC (< or =600 uM), and this cytoprotection was associated with decreased HSP70i upregulation, indicating suppression of TFEC-induced proteotoxicity. Hence, TFEC-induced necrotic cell death in the TAMH cell line is mediated by BAX and antagonized by the anti-apoptotic BCL-2 family member, BCL-xL. / S-(1,1,2,2-Tetrafluoroethyl)-L-cysteine/
Several halogenated alkenes are metabolized in part to cysteine S-conjugates, which are mitochondrial toxicants of kidney and, to a lesser extent, other organs. Toxicity is due to cysteine S-conjugate beta-lyases, which convert the cysteine S-conjugate into pyruvate, ammonia and a reactive sulfur-containing fragment. ... Mitochondrial aspartate aminotransferase and mitochondrial branched-chain aminotransferase exhibit beta-lyase activity toward S-(1,2-dichlorovinyl)-L-cysteine (the cysteine S-conjugate of trichloroethylene) and S -(1,1,2,2-tetrafluoroethyl)-L-cysteine (the cysteine S-conjugate of tetrafluoroethylene). Turnover leads to eventual inactivation of these enzymes. Here /it is reported/ that mitochondrial L-alanine-glyoxylate aminotransferase II, which, in the rat, is most active in kidney, catalyses cysteine S-conjugate beta-lyase reactions with S -(1,1,2,2-tetrafluoroethyl)-L-cysteine, S-(1,2-dichlorovinyl)-L-cysteine and S -(benzothiazolyl-L-cysteine); turnover leads to inactivation. Previous workers showed that the reactive-sulfur-containing fragment released from S-(1,1,2,2-tetrafluoroethyl) L-cysteine and S -(1,2-dichlorovinyl)-L-cysteine is toxic by acting as a thioacylating agent - particularly of lysine residues in nearby proteins. Toxicity, however, may also involve 'self-inactivation' of key enzymes. The present findings suggest that alanine-glyoxylate aminotransferase II may be an important factor in the well-established targeting of rat kidney mitochondria by toxic halogenated cysteine S-conjugates. Previous reports suggest that alanine-glyoxylate aminotransferase II is absent in some humans, but present in others. Alanine-glyoxylate aminotransferase II may contribute to the bioactivation (toxification) of halogenated cysteine S-conjugates in a subset of individuals exposed to halogenated alkenes. / S-(1,1,2,2-Tetrafluoroethyl)-L-cysteine/
Keine Reaktionsaufzeichnungen unter den aktuellen Filterkriterien.
Wird geladen…
Insoluble (NTP, 1992)
In water, 1.59X10+2 mg/L at 25 °C
Solubility in water, mg/l at 25 °C: 159 (very slightly soluble)
-105.3 °F at 760 mmHg (NTP, 1992)
-75.9 °C
-75.9 °C
-105.3 °F
-75.9 °C @760 [mm Hg]
When heated to decomposition it emits highly toxic fumes of /fluorine/.
Decomposes explosively under pressures greater than 2025 mm Hg (2.66 atm). /Tetrafluoroethylene, inhibited/
-224.5 °F (NTP, 1992)
-131.15 °C
ODORLESS OR FAINT ODOR; CRITICAL TEMP: 92 °F= 33 °C= 306 DEG K; HEAT OF POLYMERIZATION: -450 BTU/LB= 250 CAL/G= -10.5X10+5 JOULES/KG; CRITICAL PRESSURE: 573 PSIA= 38.9 ATM= 3.95 MN/SQ M; HEAT OF COMBUSTION: -4,000 BTU/LB= -2,000 CAL/G= -90X10+5 JOULES/KG /INHIBITED/
-131.2 °C
-224.5 °F
-131.15 °C
Inhalation causes irritation of respiratory system. Contact with eyes causes slight irritation. (USCG, 1999)
· Vapors may cause dizziness or asphyxiation without warning, especially when in closed or confined areas.
In acute animal studies, causes kidney injury at concentrations of 2000 to 6000 ppm; In chronic animal studies, causes hepatic tumors and renal degeneration at 156 ppm and malignant liver and kidney tumors at 312 ppm; [ACGIH] A simple asphyxiant at high concentrations; [NJ-HSFS] Tetrafluoroethylene is a skin irritant. [Quick CPC] Causes somnolence in lethal-dose inhalation studies of mice and guinea pigs; [RTECS] Tetrafluoroethylene, stabilized (UN1081) has warning of explosive polymerization; [ERG 2016]
European Commission, ESIS; IUCLID Dataset, Tetrafluoroethylene (116-14-3) (2000 CD-ROM edition) contains information on use, toxicology, and environmental effects of this chemical as supplied to the European Union by industry.[Available from, as of October 7, 2010: http://esis.jrc.ec.europa.eu/]
National Toxicology Program. Eleventh Report on Carcinogens (2005). The Report on Carcinogens is an informational scientific and public health document that identifies and discusses substances (including agents, mixtures, or exposure circumstances) that may pose a carcinogenic hazard to human health. Tetrafluoroethylene (116-14-3) is reasonably anticipated to be a human carcinogen.[Available from, as of July 31, 2009: http://ntp.niehs.nih.gov/ntp/roc/eleventh/profiles/s170tfe.pdf]
Pursuant to section 8(d) of TSCA, EPA promulgated a model Health and Safety Data Reporting Rule. The section 8(d) model rule requires manufacturers, importers, and processors of listed chemical substances and mixtures to submit to EPA copies and lists of unpublished health and safety studies. Ethene, tetrafluoro- is included on this list. Effective date 4/29/83; Sunset date: 4/29/93.
Manufacturers and processors of tetrafluoroethene are required to conduct health effects testing under TSCA section 4.
Excerpt from ERG Guide 116 [Gases - Flammable (Unstable); polymerization hazard]:
Evacuate area, fight fires only from an explosion-resistant location. Shut off supply; if not possible and no risk to surroundings, let the fire burn itself out. In other cases extinguish with water spray. In case of fire: keep cylinder cool by spraying with water.
Fresh air, rest. Seek medical attention if you feel unwell.
ON FROSTBITE: rinse with plenty of water, do NOT remove clothes. Refer immediately for medical attention.
ON FROSTBITE: rinse with plenty of water. Refer immediately for medical attention.
· CALL 911. Then call emergency response telephone number on shipping paper. If shipping paper not available or no answer, refer to appropriate telephone number listed on the inside back cover.
· ELIMINATE all ignition sources (no smoking, flares, sparks or flames) from immediate area.
EYES: First check the victim for contact lenses and remove if present. Flush victim's eyes with water or normal saline solution for 20 to 30 minutes while simultaneously calling a hospital or poison control center. Do not put any ointments, oils, or medication in the victim's eyes without specific instructions from a physician. IMMEDIATELY transport the victim after flushing eyes to a hospital even if no symptoms (such as redness or irritation) develop.
General First Aid:
Under prolonged exposure to fire or intense heat the containers may rupture violently and rocket. /Tetrafluoroethylene, stabilized/
Vapors are heavier than are and may travel to a source of ignition and glash back. /Tetrafluoroethylene, inhibited/
If material on fire or involved in fire: Do not extinguish fire unless flow can be stopped. Use water in flooding quantities as fog. Cool all affected containers with flooding of water. Apply water from as far a distance as possible. /Tetrafluoroethylene, stabilized/
Vapors are heavier than air and will collect in low areas. Vapors may travel long distances to ignition sources and flashback. Vapors in confined areas may explode when exposed to fire. Containers may explode in fire. Storage containers and parts of containers may rocket great distances, in many directions. If material or contaminated runoff enters waterways, notify downstream users of potentially contaminated waters. Notify local health and fire officials and pollution control agencies. From a secure, explosion-proof location, use water spray to cool exposed containers. If cooling streams are ineffective (venting sound increased in volume and pitch, tank discolors or shows any signs of deforming), withdraw immediately to a secure position. If cylinders are exposed to excessive heat from fire or flame contact, withdraw immediately to a secure location ... The only respirators recommended for fire fighting are self-contained breathing apparatuses that have full facepieces and are operated in a pressure-demand or other positive-pressure mode.
/Cylinders containing tetrafluoroethylene under high pressure/ ... should be stored in a cool, well-ventilated area & protected against accidental impacts.
Store in a cool, dry, well-ventilated location. Separate from oxidizing materials, air, sulfur trioxide, halogen compounds. Outside or detached storage is preferred. /Tetrafluoroethylene, inhibited/
Eliminate all ignition sources. Stop or control the leak, if this can be done without undue risk. Use appropriate foam to blanket release and suppress vapors. Use water spray to cool and disperse vapors and protect personnel. Approach release from upwind. Absorb in noncombustible material for proper disposal. /Tetrafluoroethylene, inhibited/
SRP: The most favorable course of action is to use an alternative chemical product with less inherent propensity for occupational harm/injury/toxicity or environmental contamination. Recycle any unused portion of the material for its approved use or return it to the manufacturer or supplier. Ultimate disposal of the chemical must consider: the material's impact on air quality; potential migration in soil or water; effects on animal and plant life; and conformance with environmental and public health regulations.
TERRESTRIAL FATE: Based on a classification scheme(1), an estimated Koc value of 95(SRC), determined from a structure estimation method(2), indicates that tetrafluoroethylene is expected to have high mobility in soil(SRC). Volatilization of tetrafluoroethylene from moist soil surfaces is expected to be an important fate process(SRC) given an estimated Henry's Law constant of 0.63 atm-cu m/mole(SRC), based upon its vapor pressure, 2.45X10+4 mm Hg(3), and water solubility, 159 mg/L(4). Tetrafluoroethylene is expected to volatilize from dry soil surfaces(SRC) based upon its vapor pressure(3). Biodegradation data were not available(SRC, 2010).
AQUATIC FATE: Based on a classification scheme(1), an estimated Koc value of 95(SRC), determined from a structure estimation method(2), indicates that tetrafluoroethylene is not expected to adsorb to suspended solids and sediment(SRC). Volatilization from water surfaces is expected(3) based upon an estimated Henry's Law constant of 0.63 atm-cu m/mole(SRC), derived from its vapor pressure, 2.45X10+4 mm Hg(4), and water solubility, 159 mg/L(5). Using this Henry's Law constant and an estimation method(3), volatilization half-lives for a model river and model lake are 3 hours and 4 days, respectively(SRC). According to a classification scheme(6), an estimated BCF of 3(SRC), from an estimated log Kow of 1.21(7) and a regression-derived equation(8), suggests the potential for bioconcentration in aquatic organisms is low(SRC). Biodegradation data were not available(SRC, 2010).
ATMOSPHERIC FATE: According to a model of gas/particle partitioning of semivolatile organic compounds in the atmosphere(1), tetrafluoroethylene, which has a vapor pressure of 2.45X10+4 mm Hg at 25 °C(2), is expected to exist solely as a gas in the ambient atmosphere. Gas-phase tetrafluoroethylene is degraded in the atmosphere by reaction with photochemically-produced hydroxyl radicals(SRC); the half-life for this reaction in air is estimated to be 17 hours(SRC), calculated from its rate constant of 1.13X10-11 cu cm/molecule-sec at 298 K(3). Gas-phase tetrafluoroethylene will be degraded in the atmosphere by reaction with ozone(3,4) and nitrate radicals(3). The rate constant for the vapor-phase reaction of tetrafluoroethylene with photochemically-produced hydroxyl radicals has been estimated as 1.13X10-11 cu cm/molecule-sec at 298 K(1). The rate constant for the vapor-phase reaction of tetrafluoroethylene with ozone has been reported as 4.8X10-21 cu cm/molecule-sec at 298 K(1). The Global Warming Potential is considered to be negligible(5). Tetrafluoroethylene does not contain chromophores that absorb at wavelengths >290 nm(6), and therefore is not expected to be susceptible to direct photolysis by sunlight(SRC).
Dizziness. Headache. Visual disturbances. Suffocation. Unconsciousness.
ON CONTACT WITH LIQUID: FROSTBITE.
ON CONTACT WITH LIQUID: FROSTBITE.
The following link will take the user to the National Toxicology Program (NTP) Test Agent Search Results page, which tabulates all of the "Standard Toxicology & Carcinogenesis Studies", "Developmental Studies", and "Genetic Toxicity Studies" performed with this chemical. Clicking on the "Testing Status" link will take the user to the status (i.e., in review, in progress, in preparation, on test, completed, etc.) and results of all the studies that the NTP has done on this chemical.[Available from: http://ntp-apps.niehs.nih.gov/ntp_tox/index.cfm?fuseaction=ntpsearch.searchresults&searchterm=116-14-3]
Using a structure estimation method based on molecular connectivity indices(1), the Koc of tetrafluoroethylene can be estimated to be 95(SRC). According to a classification scheme(2), this estimated Koc value suggests that tetrafluoroethylene is expected to have high mobility in soil.
Subchronic toxicity was evaluated in groups of 10 male CD rats and 10 male Syrian hamsters exposed by inhalation to 0, 101, 500, 991, or 2489 ppm tetrafluoroethylene (referred to as TFE, 99.3% minimum purity) 6 hrs/day, 5 days/week for 2 weeks. No clinical signs of toxicity resulting from TFE exposures were observed in rats and hamsters during the treatment period. After termination of exposure, rats exhibited a statistically significant decrease in serum albumin and albumin/globulin ratios at all exposure levels, although the effect was not dose related. Urinary fluoride in rats was elevated in a dose dependent manner at all levels, but differences were only significant in the 500,991 and 2489 ppm exposure groups. Other differences noted in rats included significant and dose dependent decreases in serum glutamic-pyruvic transaminase activity and urea nitrogen levels at the 500, 991 and 2489 ppm dose levels. Additionally, rats showed a significant depression in serum alkaline phosphatase activity in the 2489 ppm group. After 14 days of recovery all effects had disappeared in rats, except elevation of urinary fluoride. After termination of exposure, hamsters exhibited a significant increase in urinary fluoride excretion in the 991 and 2489 ppm groups. Serum albumin depression was significant in the 101 ppm exposure group. After the 14 day recovery period serum albumin depression was significant in the 500,991, and 2489 ppm exposure groups; urinary fluoride was at normal levels. Following 10 exposures, 5 of 5 rats exposed at the 2489 ppm level exhibited compound related kidney histopathology which disappeared after 14 days of recovery. No histopathological effects were observed in hamsters after 10 exposures, however, following the 14 day recovery period a significant increase in testicular atrophy was observed in the 2489 exposure group. Rats showed significant elevation of absolute and relative weights of liver and kidneys following the 10th exposure in the 991 and 2489 ppm exposure groups. These effects were not present after the 14 day recovery period. There were no significant differences in absolute or relative organ weights in hamsters exposed to any level of TFE.
Subchronic toxicity was evaluated in groups of 120 (60 male, 60 female) CD rats and Syrian hamsters exposed to nominal concentrations of 0, 200, 600, or 2000 ppm tetrafluoroethylene vapor (purity not reported) 6 hrs/day, 5 days/week for approx. 90 days. The following statistically significant clinical effects were observed in rats: lower mean body weights during most of the study, and lower overall body weight gains for male and females at 2000 ppm; higher incidence of alopecia and sores for animals in the 2000 ppm group; exposure related increases in urinary fluoride levels in males and females; increased urine volume in females exposed to 600 or 2000 ppm TFE with accompanying decreases in osmolality in the 200 and 2000 ppm groups; and decreased creatinine in all treated females. The only significant clinical observation reported in hamsters was an increase in the frequency of ocular abnormalities (scabs over eyes) in females exposed to 600 or 2000 ppm TFE. Rats showed the following significant blood related effects: a decrease in the serum albumin/globulin ratio at 45 days in all treated females; decreased serum albumin in 600 and 2000 ppm females at 45 days, and in 2000 ppm females at 90 days; elevated serum glutamic-pyruvic transaminase activity in females exposed at the 2000 ppm level; decreased hematocrits in 200 and 2000 ppm male rats, with decreased mean corpuscular volumes in 2000 ppm male rats; and temporarily elevated leukocyte counts in the 600 and 2000 ppm female rats. The only significant hematological effect reported in hamsters was a decrease in serum albumin in 2000 ppm males at 90 days. Following necropsy, significant observations in rats included a dose related increase in kidney and liver weights at the 2000 ppm level, and tubular nephrosis of the straight portions of the proximal convoluted tubules in animals exposed to 600 or 2000 ppm TFE, observed at 45 and 90 days. Observations in hamsters included a dose related increase in mean relative liver weights in females; and atrophic changes in immature or mature testes of hamsters exposed to 2000 ppm TFE.
/SIGNS AND SYMPTOMS/ Short Term Exposure: tetrafluoroethylene can affect you when breathed in. Irritates the eyes, skin, and respiratory tract. Very high exposures can displace the oxygen in the air, causing lightheadedness, dizziness, poor coordination, and unconsciousness. High levels may also damage the liver and/or kidneys and irritate the lungs. Contact with liquefied gas may cause frostbite. Long Term Exposure: May cause lung irritation; bronchitis may develop. May cause kidney and liver damage.
/SIGNS AND SYMPTOMS/ Toxic by-product gases /of tetrafluoroethylene/ all produce pulmonary edema ...
Tetrafluoroethylene
Group 2A: Probably carcinogenic to humans
Volume 19: (1979) Some Monomers, Plastics and Synthetic Elastomers, and Acrolein
2017
2014
NB Overall evaluation upgraded to Group 2A on the basis of sufficient evidence in experimental animals with a striking and atypical pattern of tumours
An estimated BCF of 3 was calculated in fish for tetrafluoroethylene(SRC), using an estimated/ log Kow of 1.21(1) and a regression-derived equation(2). According to a classification scheme(3), this BCF suggests the potential for bioconcentration in aquatic organisms is low(SRC).
The Henry's Law constant for tetrafluoroethylene is estimated as 0.63 atm-cu m/mole(SRC) derived from its vapor pressure, 2.45X10+4 mm Hg(1), and water solubility, 159 mg/L(2). This Henry's Law constant indicates that tetrafluoroethylene is expected to volatilize rapidly from water surfaces(3). Based on this Henry's Law constant, the volatilization half-life from a model river (1 m deep, flowing 1 m/sec, wind velocity of 3 m/sec)(3) is estimated as 3 hours(SRC). The volatilization half-life from a model lake (1 m deep, flowing 0.05 m/sec, wind velocity of 0.5 m/sec)(3) is estimated as 4 days(SRC). Tetrafluoroethylene's estimated Henry's Law constant indicates that volatilization from moist soil surfaces may occur(SRC). The potential for volatilization of tetrafluoroethylene from dry soil surfaces may exist(SRC) based upon its vapor pressure(1).
Pursuant to section 8(d) of TSCA, EPA promulgated a model Health and Safety Data Reporting Rule. The section 8(d) model rule requires manufacturers, importers, and processors of listed chemical substances and mixtures to submit to EPA copies and lists of unpublished health and safety studies. Ethene, tetrafluoro- is included on this list. Effective date 4/29/83; Sunset date: 4/29/93.
Manufacturers and processors of tetrafluoroethene are required to conduct health effects testing under TSCA section 4.
Tetrafluoroethylene
1
10000
Flammable chemical that can be released at a facility.
Several haloalkenes are metabolized in part to nephrotoxic cysteine S-conjugates; for example, ... tetrafluoroethylene /is/ converted to ... S-(1,1,2,2-tetrafluoroethyl)-L-cysteine (TFEC) ... Most halogenated cysteine S-conjugates are metabolized by cysteine S-conjugate beta-lyases to pyruvate, ammonia, and an alpha-chloroenethiolate or an alpha-difluoroalkylthiolate (with TFEC) that may eliminate halide to give a thioacyl halide, which reacts with epsilon-amino groups of lysine residues in proteins. Nine mammalian pyridoxal 5'-phosphate (PLP)-containing enzymes catalyze cysteine S-conjugate beta-lyase reactions, including mitochondrial aspartate aminotransferase (mitAspAT), and mitochondrial branched-chain amino acid aminotransferase (BCAT(m)). Most of the cysteine S-conjugate beta-lyases are syncatalytically inactivated. TFEC-induced toxicity is associated with covalent modification of several mitochondrial enzymes of energy metabolism. Interestingly, the alpha-ketoglutarate- and branched-chain alpha-keto acid dehydrogenase complexes (KGDHC and BCDHC), but not the pyruvate dehydrogenase complex (PDHC), are susceptible to inactivation. mitAspAT and BCAT(m) may form metabolons with KGDHC and BCDHC, respectively, but no PLP enzyme is known to associate with PDHC. Consequently, /it was hypothesized/ that not only do these metabolons facilitate substrate channeling, but they also facilitate toxicant channeling, thereby promoting the inactivation of proximate mitochondrial enzymes and the induction of mitochondrial dysfunction. /S-(1,1,2,2-tetrafluoroethyl)-L-cysteine/
Tetrafluoroethylene was metabolized to S-(1,1,2,2-tetrafluoroethyl)glutathione by rat liver fractions in vitro; the reaction was catalyzed by both microsomal and cytosolic glutathione S-transferases. The rate with microsomes was four times that with cytosol fractions. Evidence for this metabolic pathway in vivo has been obtained by the identification of the cysteinylglycine and cysteine conjugates of tetrafluoroethylene in rat bile. Cytochrome P-450 oxidation, a common metabolic route for haloalkenes, does not appear to occur in the metabolism of tetrafluoroethylene ... When administered po to rats, the synthetic cysteine conjugate of tetrafluoroethylene causes renal damage identical to that caused by tetrafluoroethylene itself. The conjugate was metabolized by renal slices in vitro giving pyruvate, ammonia, and a reactive species which caused marked inhibition of organic ion transport into slices. Purified renal beta-lyase also cleaved this conjugate giving stoichiometric amounts of pyruvate and ammonia ... The nephrotoxicity of tetrafluoroethylene is believed to derive from the hepatic glutathione conjugate of this compound. Following excretion and degradation of this conjugate in bile, the cysteine conjugate is reabsorbed and further metabolized in the kidney by the enzyme beta-lyase to a cytotoxic species.
The metabolism of tetrafluoroethylene has been studied in rat liver fractions; both microsomal and cytosolic glutathione S-transferases catalyze the formation of S-(1,1,2,2-tetrafluoroethyl)glutathione. The rate with microsomes was four times greater than with cytosol. Fluoride ion release was equivalent to approximately 20% of the glutathione used. The quantities of glutathione used and of fluoride ion released in incubations were identical whether cytochrome P450 was active or had been inactivated with carbon monoxide. Thus, cytochrome P450 oxidation, a pathway common to many haloalkenes, does not appear to be involved in the metabolism of tetrafluoroethylene. Evidence for the glutathione conjugation pathway in vivo comes from the identification of the cysteinylglycine and cysteine conjugates of tetrafluoroethylene in rat bile, following oral administration of L-[35S]cysteine and then inhalation exposure to 6000 ppm [24 600 mg/cu m] tetrafluoroethylene for 6 hr. S-(1,1,2,2-Tetrafluoroethyl)-L-cysteine is metabolized in vitro in rat renal cortex slices to give pyruvate and ammonia, a reaction that is catalyzed by beta-lyase and which also generates a reactive thiol that is probably important in renal cytotoxicity.
... Tetrafluoroethylcysteine to male rats ... is an important metabolite in the cytotoxic response. The cytotoxicity of the cysteine conjugate has also been demonstrated in vitro in rat kidney slices by reduced uptake of both organic anion, para-aminohippuric acid and the cation, tetraethylammonium bromide.
Used to produce polytetrafluoroethylene polymers (Teflon); [ACGIH]
In prepn of propellants for food product aerosols
MONOMER FOR POLYTETRAFLUOETHYLENE RESINS; CHEM INT FOR HEXAFLUOROPROPYLENE; COMONOMER FOR PERFLUOROALKOXY RESINS, FLUORINATED ETHYLENE-PROPYLENE RESINS, & ETHYLENE-TETRAFLUOROETHYLENE RESINS; TERMONOMER WITH VINYLIDENE FLUORIDE & HEXAFLUOROPROPYLENE
Used as a copolymer with hexafluoropropylene to substitute for polytetrafluoroethylene
It is used mainly for the production of fluoropolymers. It reacts with perfluoronitrosoalkanes to produce so-called nitroso rubbers. It is also used in the production of low molecular mass compounds and intermediates, for example, for the manufacture of iodoperfluoroalkanes.
Principal industrial use of CF2:CF2 is for preparation of polytetrafluoroethylene (Teflon (R)) Resins and copolymers.
2023: 10,000,000 - <50,000,000 lb
(1972) GREATER THAN 6X10+9 GRAMS
(1975) GREATER THAN 5.90X10+9 GRAMS
Ethene, tetrafluoro- is listed as a High Production Volume (HPV) chemical (65FR81686). Chemicals listed as HPV were produced in or imported into the U.S. in >1 million pounds in 1990 and/or 1994. The HPV list is based on the 1990 Inventory Update Rule. (IUR) (40 CFR part 710 subpart B; 51FR21438).
Production volumes for non-confidential chemicals reported under the Inventory Update Rule. [Table#2279]
Production volume for non-confidential chemicals reported under the 2006 Inventory Update Rule. Chemical: Ethene, 1,1,2,2-tetrafluoro-. Aggregated National Production Volume: 50 to < 100 million pounds.
AT LEAST TWO-THIRDS USED AS A MONOMER FOR POLYTETRAFLUOROETHYLENE RESINS (1974)
REFRIGERANTS, 39%; FOAM BLOWING AGENTS, 17%; SOLVENTS, 14%; FLUOROPOLYMERS, 14%; STERILANT GAS, 2%; AEROSOL PROPELLANTS, 2%; FOOD FREEZANT, 1%; OTHER, 8%; EXPORTS, 3% (1985) /FLUOROCARBONS/
... /It/ is produced by pyrolysis of chlorodifluoromethane (CHClF2) or of trifluoromethane (CHF3).
... Any source of fluorine will combine with carbon at temperature greater than 1500 °C to form difluorocarbene radicals (-CF2-) which combine under appropriate conditions to give a large yield of CF2:CF2.
By passing chlorodifluoromethane through a hot tube.
Tetrafluoroethylene is manufactured in a four step process involving the independent production of hydrogen fluoride and chloroform. These products are subsequently reacted in the presence of antimony trifluoride to form chlorodifluoromethane. Finally, chlorodifluoromethane is pyrolysed at 590-900 °C to produce a yield of 95% tetrafluoroethylene
All Other Basic Organic Chemical Manufacturing
Ethene, 1,1,2,2-tetrafluoro-: ACTIVE
Monomer of the plastic, polytetrafluoroethylene.
Can polymerize in absence of inhibitor, especially when heated or in presence of oxygen. /Inhibited/
It can ... be dimerized under appropriate conditions of temp and pressure to octafluorocyclobutane ... which is a stable and practically non-toxic propellant for food product aerosols.
The ability of tetrafluoroethylene to induce specific locus mutations at the HPRT locus in cultured Chinese hamster ovary (CHO) cells (CHO/HPRT Mutagenicity Assay) was evaluated in the presence and absence of Aroclor-induced rat liver S9 metabolic activation. Based on preliminary toxicity determinations, tetrafluoroethylene, was tested at nominal concentrations of 0, 20, 40, 60, 80 and 100% for treatments with and without metabolic activation. Twenty two nonactivated cultures produced a range of 100.0 - 56.5% cell survival relative to the negative control and twenty two activated cultures produced a range of 133.4 - 49.3% relative cell survival. None of the cultures produced mutant frequencies significantly greater than the negative control with or without metabolic activation.
The mutagenicity of tetrafluoroethylene was evaluated Salmonella tester strains TA1535, TA97, TA98 and TA100 (Ames Test), both in the presence and absence of Aroclor-induced rat liver S9 metabolic activation. Based on preliminary toxicity determinations, tetrafluoroethylene, was tested at nominal concentrations of 0, 0.5, 3, 4, and 5% using the plate incorporation technique. Tetrafluoroethylene did not cause a positive response in any tester strain with or without metabolic activation.