9003-20-7C=CC(=O)OCXTXRWKRVRITETP-UHFFFAOYSA-NVinyl acetate is an industrial chemical that is produced in large amounts in the United States. It is a clear, colorless liquid with a sweet, fruity smell. It is very flammable and may be ignited by heat, sparks, or flames. Vinyl acetate is used to make other industrial chemicals. These chemicals are used mainly to make glues for the packaging and building industries. They are also used to make paints, textiles, and paper. Vinyl acetate is also used as a coating in plastic films for food packaging and as a modifier of food starch.
9003-20-7CHEMBL1470323CHEBI:46916Hazardous Air Pollutants (HAPs)
Other Classes -> Esters, Other
Carcinogens
Volatile Organic Compound (VOC)
log Kow = 0.73
0.73
0.73
0.6
0.932 at 68 °F (EPA, 1998) - Less dense than water; will float
0.932 at 20 °C/4 °C
Relative density (water = 1): 0.93
0.93
0.9256 @25 °C
0.93
Danger
H225: Highly Flammable liquid and vapor [Danger Flammable liquids]
P203, P210, P233, P240, P241, P242, P243, P261, P271, P280, P303+P361+P353, P304+P340, P317, P318, P319, P370+P378, P403+P233, P403+P235, P405, and P501 (click each P-code to see the statement)
This chemical does not meet GHS hazard criteria for < 0.1% (1 of 2185) of reports.
Danger
H225 (> 99.9%): Highly Flammable liquid and vapor [Danger Flammable liquids]
Chemical: Acetic acid, ethenyl ester
Hazard Traits - Carcinogenicity; Respiratory Toxicity
Regulation (EC) No 1935/2004 (amended)
Acetic acid ethenyl ester is listed on the EPA's Chemical Data Reporting (CDR) system. Manufacturers and importers of Acetic acid ethenyl ester 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: 11-05-2023 https://echa.europa.eu/registration-dossier/-/registered-dossier/15530
Acetic acid ethenyl ester: HSNO Approval: HSR001235 Approved with controls
When heated to decomposition, it burns and emits acrid fumes. Highly dangerous when exposed to heat, flames or oxidizers; explosion hazard with strong acids and strong oxidizers. Incompatible with alumina, oxidizing materials, 2-aminoethanol, chlorosulfonic acid; ethyleneimine; 36% hydrochloric acid; 48.7% hydrofluoric acid; 70% nitric acid; oleum; 96% sulfuric acid; ethylene diamine; peroxides and silica gel. Avoid light or any polymerizing initiator. Hazardous polymerization can be initiated by organic and inorganic peroxides; azo compounds; redox systems (including organometallic components); light; and high energy radiation. (EPA, 1998)
/It has been suggested that/ vinyl acetate disturbs glutathione metabolism, ... by acting as a substrate for glutathione transferase.
Acetaldehyde is a metabolite of vinyl acetate through esterase-mediated metabolism. It is discussed that vinyl acetate exhibits its genotoxicity via acetaldehyde. For example /researchers/ demonstrated that vinyl acetate induces /DNA protein crosslinking/ via acetaldehyde, and ... chromosomal damage induced by vinyl acetate in mammalian cell cultures is through formation of acetaldehyde ... Acetaldehyde is a naturally occurring substance in the metabolic pathways of animals and humans (metabolism of ethanol and sugars). It occurs in small quantities in human blood. Therefore, it may well be that acetaldehyde expresses its genotoxic potential in case of metabolic overload.
Whole body (animal studies): less than 6 hours; [TDR, p. 1218]
... The half-life of /200 uM/ vinyl acetate elimination in human whole blood was 4.1 minutes as compared to /less than/ 1 minute in rat whole blood.
... /On/ hydrolysis /in the blood/, vinyl acetate yields acetic acid, a normal body constituent, and vinyl alcohol, which should rapidly tautomerize to yield acetaldehyde, another normal body constituent.
The hydrolysis of vinyl acetate was studied in vitro with rat liver and lung microsomes, rat and human plasma and purified esterases (acetylcholine esterase, butyrylcholine esterase, carboxyl esterase). Characterization of the kinetic parameters revealed that rat liver microsomes and purified carboxyl esterase (from porcine liver) displayed the highest activity. In order to establish the rate of metab of vinyl acetate in vivo, rats were exposed in closed desiccator jar chambers, and gas uptake kinetics were studied. The decay of vinyl acetate was dose-dependent, indicating possible satn of metabolic pathway(s). The maximal clearance (at lower concn) of vinyl acetate from the system (30,000 mL/hr/kg) was similar to the maximal ventilation rate in this species. The exposure of rats to vinyl acetate resulted in a transient exhalation of significant amts of acetaldehyde into the closed exposure system.
Gas chromatographic analysis of human whole-blood lymphocyte cultures treated for 10 seconds to 20 min with vinyl acetate (5.4 mM) revealed a rapid degradation of vinyl acetate and formation of acetaldehyde. During the 20 min observation period, no degradation of vinyl acetate or formation of acetaldehyde were observed in complete culture medium without blood, which suggested that the reaction was enzymatic.
Keine Reaktionsaufzeichnungen unter den aktuellen Filterkriterien.
Wird geladen…
COLORLESS, MOBILE LIQUID
Clear, colorless liquid
2 % (NIOSH, 2024)
Sol in ethane, acetone, chloroform
Soluble in organic liquids
> 10% in ethyl ether; > 10% in ethanol; > 10% in benzene
At 20 °C, a saturated solution of vinyl acetate in water contains 2.0-2.4 wt % vinyl acetate, whereas a saturated solution of water in vinyl acetate contains 0.9-1.0 wt % water; at 50 °C, the solubility of vinyl acetate in water is 0.1 wt % more than at 20 °C, but the solubility of water in vinyl acetate doubles to about 2 wt %
For more Solubility (Complete) data for VINYL ACETATE (7 total), please visit the HSDB record page.
18 °F (EPA, 1998)
-8 °C, closed cup
-8 °C, 18 °F (CLOSED CUP)
0.5-0.9 °C (open cup)
-8 °C c.c.
18 °F
· HIGHLY FLAMMABLE: Will be easily ignited by heat, sparks or flames.
Highly flammable. Vapour/air mixtures are explosive. Heating will cause rise in pressure with risk of bursting.
It is a highly flammable liq and a dangerous fire hazard.
Highly dangerous fire hazard when exposed to heat, flame or oxidizers.
Vinyl acetate has been related to reproductive abnormalities. It is a skin and upper respiratory tract irritantand a central nervous system depressant. Exposure caused gradual deterioration of heart muscles. (EPA, 1998)
· May cause toxic effects if inhaled or absorbed through skin.
Vinyl acetate is an industrial chemical that is produced in large amounts in the United States. It is a clear, colorless liquid with a sweet, fruity smell. It is very flammable and may be ignited by heat, sparks, or flames. Vinyl acetate is used to make other industrial chemicals. These chemicals are used mainly to make glues for the packaging and building industries. They are also used to make paints, textiles, and paper. Vinyl acetate is also used as a coating in plastic films for food packaging and as a modifier of food starch.
Vinyl acetate is primarily used as a monomer in the production of polyvinyl acetate and polyvinyl alcohol. Acute (short-term) inhalation exposure of workers to vinyl acetate has resulted in eye irritation and upper respiratory tract irritation. Chronic (long-term) occupational exposure did not result in any severe adverse effects in workers; some instances of upper respiratory tract irritation, cough, and/or hoarseness were reported. Nasal epithelial lesions and irritation and inflammation of the respiratory tract were observed in mice and rats chronically exposed by inhalation. No information is available on the reproductive, developmental, or carcinogenic effects of vinyl acetate in humans. An increased incidence of nasal cavity tumors has been observed in rats exposed by inhalation. In one drinking water study, an increased incidence of tumors was reported in rats. EPA has not classified vinyl acetate for carcinogenicity.
Vinyl acetate causes eye and respiratory irritation in production workers. Experimental animals show minor elevation of liver function tests after IP injection and central nervous system depression after inhalation; [ACGIH] A lachrymator; [CHEMINFO] May cause skin redness and blisters; A skin, eye, and respiratory tract irritant; [ICSC] Vinyl acetate, stabilized (UN1301) has warning of explosive polymerization; [ERG 2016]
1301 129P
1301 129P
Wear self-contained (positive pressure if available) breathing apparatus and full protective clothing. Spray cooling water on containers that are exposed to flames until well after the fire is out. For massive fire in cargo area, use unmanned hose holder or monitor nozzles; if this is impossible, withdraw from area and let fire burn. Withdraw immediately in case of rising sound from venting safety device or any discoloration of tank due to fire. Isolate for 1/2 mile in all directions if tank car or truck is involved in fire. Small fires: extinguish with dry chemical, carbon dioxide, water spray, fog, or alcohol foam. Large fires: water spray, fog, or alcohol foam. (EPA, 1998)
Use alcohol-resistant foam, foam, powder, carbon dioxide, fine water spray. In case of fire: keep drums, etc., cool by spraying with water.
Fresh air, rest. Half-upright position. Refer for medical attention.
Remove contaminated clothes. Rinse skin with plenty of water or shower. Seek medical attention if you feel unwell.
First rinse with plenty of water for several minutes (remove contact lenses if easily possible), then refer for medical attention.
Rinse mouth. Give one or two glasses of water to drink. Refer 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.
Signs and Symptoms of Acute Vinyl Acetate Monomer Exposure: Vinyl acetate monomer may irritate the skin, eyes, and respiratory tract; blisters may form. Inhalation of vapors may result in dizziness or suffocation.
General First Aid:
(General first aid procedures)
Vapors are heavier than air and may travel to a source of ignition and flash back.
Flammable liquid. Moderate health hazard.
Do not extinguish fire unless flow can be stopped. Use water in flooding quantities as fog. Solid streams of water may spread fire. Apply water from as far a distance as possible. Cool all affected containers with flooding quantities of water. Use "alcohol" foam, dry chemical, or carbon dioxide.
Evacuation: If fire becomes uncontrollable or container is exposed to direct flame--consider evacuation of 0.5 (1/2) mile radius. If material leaking (not on fire) consider evacuation from downwind area based on amount of material spilled, location & weather conditions. /Vinyl acetate, inhibited/
Fight fire from protected location or maximum possible distance. Use water spray, dry chemical, "alcohol resistant" foam, or carbon dioxide. Water may be ineffective. Use water only in flooding quantities as fog. Use water spray to keep fire-exposed containers cool.
If material on fire or involved in fire: Do not extinguish fire unless flow can be stopped. Use water in flooding quantities as fog. Solid streams of water may spread fire. Cool all affected containers with flooding quantities of water. Apply water from as far a distance as possible. Use "alcohol" foam, dry chemical or carbon dioxide.
It can be stored in steel, aluminum, or stainless steel containers under nitrogen. It is not necessary to add stabilizers at lower temperatures. If the vinyl acetate is to be warmed, stabilizers, such as hydroquinone, hydroquinone monomethyl ether, or diphenylamine are added. The quantity of stabilizer used is small, e.g., 3 -20 ppm hydroquinone, so that it does not generally need to be removed during the later polymerization.
Storage Temperature: Ambient. Inert Atmosphere: No requirement.
Take precautionary measures against static discharges.
Vinyl acetate shall be stored at temperatures less than 37.8 °C (100 °F) in well-ventilated areas and kept away from ignition sources such as heat and direct sunlight. No heating apparatus capable of exceeding 80% of the autoignition temperature of vinyl acetate (427 °C) shall be used in vinyl acetate storage areas. The storage of vinyl acetate in glass containers should not be in the same areas as oxidizing agents or other incompatible chemicals. Containers of vinyl acetate shall be kept tightly closed when not in use and shall be stored so as to minimize accidental ruptures and spills.
For more Storage Conditions (Complete) data for VINYL ACETATE (8 total), please visit the HSDB record page.
Environmental considerations: land spill: Dig a pit, pond, lagoon, holding area to contain liquid or solid material. /SRP: If time permits, pits, ponds, lagoons, soak holes, or holding areas should be sealed with an impermeable flexible membrane liner./ Dike surface flow using soil, sand bags, foamed polyurethane, or foamed concrete. Absorb bulk liquid with fly ash, cement powder, sawdust, or commercial sorbents. Apply "universal" gelling agent to immobilize spill. Apply fluorocarbon-water foam to diminish vapor and fire hazard.
Environmental considerations: water spill: Use natural barriers or oil spill control booms to limit spill travel. Use surface active agent (eg detergent, soaps, alcohols), if approved by EPA. Inject "universal" gelling agent to solidify encircled spill and increase effectiveness of booms. If dissolved, in region of 10 ppm or greater concn, apply activated carbon @ ten times the spilled amount. Remove trapped material with suction hoses. Use mechanical dredges or lifts to remove immobilized masses of pollutants and precipitates.
Notify local health and wildlife officals /in case of spill/. Notify operaters of nearby water intakes /in case of spill/.
Environmental considerations--air spill: Apply water spray or mist to knock down vapors.
For more Cleanup Methods (Complete) data for VINYL ACETATE (7 total), please visit the HSDB record page.
SRP: The most favorable course of action is to use an alternative chemical product with less inherent propensity for occupational exposure 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, aquatic, and plant life; and conformance with environmental and public health regulations.
The following wastewater treatment technologies have been investigated for vinyl acetate: Concentration process: Activated Carbon.
Do not empty into drains.
Vinyl acetate is a waste chemical stream constituent which may be subjected to ultimate disposal by controlled incineration.
For more Disposal Methods (Complete) data for VINYL ACETATE (9 total), please visit the HSDB record page.
... Previous studies from our laboratory suggest that rat liver microsome-activated vinyl acetate induces plasmid DNA-histone crosslinks, in vitro, through esterase-mediated metabolism. Since nasal tissues contain high levels of carboxylesterase, tumorigenesis may be related to in situ production of the hydrolysis products acetaldehyde and acetic acid. Vinyl acetate was cytotoxic to both respiratory and olfactory tissues in vitro at 50-200 mM, but not 25 mM, after 2 hr exposure. Pretreatment of rats with the carboxylesterase inhibitor, bis-(p-nitrophenyl) phosphate (BNPP), attenuated the cytotoxic effects and metabolism of vinyl acetate in both tissue types. Semicarbazide, an aldehyde scavenger, was unable to protect the tissues from vinyl acetate-induced cytotoxicity. When the metabolites were tested, acetic acid, but not acetaldehyde, was cytotoxic to both tissues.
Respiratory (From the Nose to the Lungs)
Nervous
Eyes, skin, respiratory system
Vinyl acetate may affect the immune system. It may also be a carcinogen. (L1304)
Vinyl acetate may affect the immune system. It may also be a carcinogen. (L1304)
LC50; Species: Carassius auratus (Goldfish, length 3.8-6.4 cm, weight 1-2 g); Conditions: freshwater, static, 25 °C, pH 7.5, hardness 20 mg/L CaCO3, alkalinity 18 mg/L CaCO3, dissolved oxygen 7.8 mg/L; Concentration: 42330 ug/L for 24-96 hr (95% confidence interval: 33520-53470 ug/L) /formulation/
LC50; Species: Lepomis macrochirus (Bluegill, length 3.8-6.4 cm, weight 1-2 g); Conditions: freshwater, static, 25 °C, pH 7.5, hardness 20 mg/L CaCO3, alkalinity 18 mg/L CaCO3, dissolved oxygen 7.8 mg/L; Concentration: 18530 ug/L for 24 hr (95% confidence interval: 15730-22070 ug/L) /formulation/
LC50; Species: Lepomis macrochirus (Bluegill, length 3.8-6.4 cm, weight 1-2 g); Conditions: freshwater, static, 25 °C, pH 7.5, hardness 20 mg/L CaCO3, alkalinity 18 mg/L CaCO3, dissolved oxygen 7.8 mg/L; Concentration: 18000 ug/L for 48 and 96 hr (95% confidence interval: 15040-21540 ug/L) /formulation/
LC50; Species: Pimephales promelas (Fathead minnow, age 1 day); Conditions: freshwater, static, 25 °C, pH 8.2, hardness 172 mg/L CaCO3, alkalinity 144 mg/L CaCO3, dissolved oxygen saturated; Concentration: 14000 ug/L for 24 hr /formulation/
For more Ecotoxicity Values (Complete) data for VINYL ACETATE (36 total), please visit the HSDB record page.
TERRESTRIAL FATE: Based on a classification scheme(1), an estimated Koc value of 60(SRC), determined from a log Kow of 0.73(2) and a regression-derived equation(3), indicates that vinyl acetate is expected to have high mobility in soil(SRC). Volatilization of vinyl acetate from moist soil surfaces is expected to be an important fate process(SRC) given an estimated Henry's Law constant of 5.1X10-4 atm-cu m/mole(SRC), derived from its vapor pressure, 90.2 mm Hg(4), and water solubility, 20,000 mg/L(5). However, a hydrolysis half-life of 7.3 days (25 °C and pH 7)(6) indicates that hydrolysis may occur in moist soils and is expected to attenuate leaching in the soil column(SRC). Vinyl acetate is expected to volatilize from dry soil surfaces(SRC) based upon its vapor pressure(4). Vinyl acetate readily polymerizes; therefore, if vinyl acetate is released to the environment, polymerization may occur(SRC). Complete biodegradation of vinyl acetate occurred using a soil inoculum within 26 hours under both anaerobic and aerobic conditions; acetaldehyde and acetate were formed as reaction products under both oxygen conditions(7). This suggests that biodegradation may be an important environmental fate process in soil(SRC).
AQUATIC FATE: Based on a classification scheme(1), an estimated Koc value of 60(SRC), determined from a log Kow of 0.73(2) and a regression-derived equation(3), indicates that vinyl acetate 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 5.1X10-4 atm-cu m/mole(SRC), derived from its vapor pressure, 90.2 mm Hg(4), and water solubility, 20,000 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 4 hours and 4 days, respectively(SRC). According to a classification scheme(6), an estimated BCF of 3.2(SRC), from its log Kow(2) and a regression-derived equation(7), suggests the potential for bioconcentration in aquatic organisms is low(SRC). Vinyl acetate is degraded in natural water by hydrolysis with an estimated hydrolysis half-life at 25 °C and pH 7 of 7.3 days(8); the hydrolysis rate increases as the pH increases(8). Reaction with hydroxyl radicals and singlet oxygen in natural water may proceed with half-lives of approximately 13 and 8 days, respectively, based on rates determined for olefinic structures(9). A 98% of theoretical BOD was reported using activated sludge in the Japanese MITI test(10), suggesting that biodegradation may be an important environmental fate process in water(SRC).
ATMOSPHERIC FATE: According to a model of gas/particle partitioning of semivolatile organic compounds in the atmosphere(1), vinyl acetate, which has a vapor pressure of 90.2 mm Hg at 20 °C(2), is expected to exist solely as a vapor in the ambient atmosphere(SRC). Vapor-phase vinyl acetate 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 14 hours(SRC) calculated from its rate constant of 2.50X10-11 cu cm/molecule-sec at 25 °C(3). Vapor-phase vinyl acetate may also be degraded in the atmosphere by reaction with ozone(4); the half-life for this reaction in air is estimated to be 3.9 days(SRC).
The substance can be absorbed into the body by inhalation, through the skin and by ingestion.
inhalation, ingestion, skin and/or eye contact
Oral (L1304) ; Inhalation (L1304) ; Dermal (L1304)
Oral (L565) ; inhalation (L565) ; dermal (L565)
Polyvinyl acetate usually contains trace amounts of its precursor, vinyl acetate. One of the metabolites of vinyl acetate, acetaldehyde, is a known animal carcinogen. Acetaldehyde can form adducts with DNA, causing damage such as cross-links. (L1304, A354)
One of the metabolites of vinyl acetate, acetaldehyde, is a known animal carcinogen. Acetaldehyde can form adducts with DNA, causing damage such as cross-links. (L1304, A354)
/AQUATIC SPECIES/ ...Three species of Lecane, a littoral rotifer, /were analyzed/ for susceptibility to six metals and four organic toxicants using a fluorometric assay based on inhibition of activity of the enzyme phospholipase A2. The metallic toxicants that we tested included Cd, Cr, Cu, Pb, Hg (as HgCl2), and Ti; the organic toxicants included benzene, ethyl acetate, toluene, and vinyl acetate. The three species differed greatly with respect to their susceptibility to the various toxicants. Lecane quadridentata, for example, was particularly sensitive to the four organic compounds (median effective concentration values [EC50] ranged from 6.6 x 10-4 to 0.987 mg/L). Lecane luna, in contrast, seemed particularly sensitive to metals (EC50 values ranged from 2 x 10-6 to 1.92 mg/L). Lecane hamata was relatively insensitive to organic solvents (EC50 values ranged from 4.25 to 126.5 mg/L).
Sore throat. Cough. Shortness of breath.
Redness. Dry skin.
Redness.
irritation eyes, skin, nose, throat; hoarseness, cough; loss of smell; eye burns, skin blisters
Inhalation of vinyl acetate irritates the eyes, nose, and throat. Skin contact causes irritation and blisters. (L1304)
Inhalation of vinyl acetate irritates the eyes, nose, and throat. Skin contact causes irritation and blisters. (L1304)
Vinyl acetate was qualitatively detected in wastewater effluents collected from the advanced waste treatment facility in Lake Tahoe, CA in Oct 1974(1). A concentration of 50 ppm was detected in a wastewater effluent from a polyvinyl acetate plant(2). Vinyl acetate was identified in municipal landfill gas at an average concentration of 5663 ppbV(3). Vinyl acetate emission factors (based on mass of fuel consumed) were measured in smoke condensates of Ponderosa pine wood (3 g/kg, smoldering; 0.05 g/kg, flaming), needles (2.0 g/kg, smoldering), bark (1 g/kg, smoldering; 0.5 g/kg, self-substained smoldering), litter (0.7 g/kg, smoldering; 0.5 g/kg, self-substained smoldering), duff (0.15 g/kg, smoldering; 0.3 g/kg, self-substained smoldering), and humus (not detected, detection limit not specified)(4). Pulverized coal combustion emission factors using a small-scale down-fired combustor were reported as follows: not detected to 4.179X10-7 lb/10+6 Btu for baseline conditions; not detected to 4.274X10-7 lb/10+6 Btu for stoichiometric ratio conditions; and 2.081X10-8 to 3.684X10-7 lb/10+6 Btu for low NOx conditions (detection limit = 10 ng per sample)(5).
Vinyl acetate can be released to the environment from industrial sources and biomass combustion(1). Waste gases from scrubbers (generated during the industrial manufacture of vinyl acetate) may contain trace levels of vinyl acetate(2). An emission factor of 6.22 ug/g vinyl acetate from extruded ethylene-vinyl acetate and vinyl acetate copolymer (28% vinyl acetate) was determined experimentally at 435 °C under laboratory conditions. All low density polyethylene and ethylene-methyl acrylate copolymers with vinyl acetate emitted >0.01 ug/g vinyl acetate at 435 °C(3).
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. Vinyl acetate is included on this list. Effective date 2/10/86; Sunset date: 2/10/96.
This action promulgates standards of performance for equipment leaks of Volatile Organic Compounds (VOC) in the Synthetic Organic Chemical Manufacturing Industry (SOCMI). The intended effect of these standards is to require all newly constructed, modified, and reconstructed SOCMI process units to use the best demonstrated system of continuous emission reduction for equipment leaks of VOC, considering costs, non air quality health and environmental impact and energy requirements. Vinyl acetate is produced, as an intermediate or final product, by process units covered under this subpart.
Listed as a hazardous air pollutant (HAP) generally known or suspected to cause serious health problems. The Clean Air Act, as amended in 1990, directs EPA to set standards requiring major sources to sharply reduce routine emissions of toxic pollutants. EPA is required to establish and phase in specific performance based standards for all air emission sources that emit one or more of the listed pollutants. Vinyl acetate is included on this list.
Persons in charge of vessels or facilities are required to notify the National Response Center (NRC) immediately, when there is a release of this designated hazardous substance, in an amount equal to or greater than its reportable quantity of 5000 lb or 2270 kg. The toll free number of the NRC is (800) 424-8802. The rule for determining when notification is required is stated in 40 CFR 302.4 (section IV. D.3.b).
Releases of CERCLA hazardous substances are subject to the release reporting requirement of CERCLA section 103, codified at 40 CFR part 302, in addition to the requirements of 40 CFR part 355. Vinyl Acetate Monomer is an extremely hazardous substance (EHS) subject to reporting requirements when stored in amounts in excess of its threshold planning quantity (TPQ) of 1,000 lbs.
Vinyl acetate is designated as a hazardous substance under section 311(b)(2)(A) of the Federal Water Pollution Control Act and further regulated by the Clean Water Act Amendments of 1977 and 1978. These regulations apply to discharges of this substance. This designation includes any isomers and hydrates, as well as any solutions and mixtures containing this substance.
Vinyl acetate monomer
1
10000
Flammable chemical that can be released at a facility.
Vinyl acetate hydrolysis has been studied in vitro in the oral mucosal tissues from the oral cavity of rats and mice. The hydrolysis activity of the oral tissues is at least 100-fold lower than that of the nasal tissues. A physiologically based pharmacokinetic model was developed which describes the deposition of vinyl acetate in the nasal cavity of the rat. This model predicts steady state concentrations of the metabolite acetic acid after continuing 6 hr-exposure in respiratory tissue which are approximately 13 times greater and in olfactory tissue which are approximately 2 times greater than those of acetaldehyde, the second metabolite. As the concentration of acids is indicative for the concentration of protons the model predicts the greatest reduction in intracellular pHi for respiratory mucosa. Hence, pH effects should be more pronounced in this tissue as compared to other tissues. This physiologically based toxicokinetic/toxicodynamic model for rat was modified for the olfactory epithelium of the both human and rat nasal cavity. The change in intracellular pH is predicted to be slightly greater for human olfactory epithelium, than that of rats. To provide validation data for this model, controlled human exposures at exposure levels of 1, 5 and 10 ppm to inhaled vinyl acetate were conducted. Air was sampled by a probe inserted into the nasopharyngeal cavity of five volunteers at bi-directional breathing through the nose. Data from ion trap mass spectrometry measurements of labeled vinyl acetate and acetaldehyde were compared with data from the human nasal model simulation. For the vinyl acetate data a good fit was demonstrated (r = 0.9).
For more Metabolism/Metabolites (Complete) data for VINYL ACETATE (8 total), please visit the HSDB record page.
Vinyl acetate may be absorbed following ingestion, inhalation, or dermal exposure, and distributes throughout the body. It is rapidly hydrolyzed by esterases in the blood to acetate and the unstable intermediate, vinyl alcohol. Vinyl alcohol is then rapidly converted to acetaldehyde, which in turn is metabolized to acetate in the liver. This in turn is incorporated into the "2 carbon pool" of normal body metabolism and eventually forms carbon dioxide as the major breakdown product, which is expired. (L1304)
... /The/ fate of inhaled vinyl acetate in rabbits /was studied/. ... Vinyl acetate tended to remain in the body after it was inhaled; 70% of the vinyl acetate administered was retained, and an equilibrium was established in the first few min after exposure began. ... No vinyl acetate /was found/ in the blood, either during or after its inhalation, which suggested ... that vinyl acetate is rapidly metabolized when it enters the body through the lungs.
When mice were exposed to (14)C-vinyl acetate, the radioactivity excretion pattern was similar to that observed with (14)C-acetaldehyde. In both cases, the majority of radioactivity was exhaled as (14)C-carbon dioxide.
Two male Wistar Rats exposed to vinyl acetate (stabilized with 0.01% hydroquinone) concentrations varying between 200 and 2000 ppm in closed chambers with an exposure time of 1.4 hr or less demonstrated dose dependent elimination kinetics. The authors concluded that the metabolic pathways became saturated when vinyl acetate exposure levels exceeded 650 ppm (2320 mg/cu m). Vinyl acetate deposition was measured in the isolated upper respiratory tract (URT) of anaesthetized adult male CrlCD:BR rats at exposure concentrations ranging from 73 to 2190 ppm during 1 hr inhalation under unidirectional flow conditions (flow rate 100 mL/min) ... Preliminary experiments showed that approximately 8 min of exposure was required for vinyl acetate to achieve a steady state in nasal tissues. After 8 min of equilibration, impinger samples were collected, approximately every 4 min, for up to 40 min and analyzed for vinyl acetate and acetaldehyde by gas chromatography ... Acetaldehyde was found in expired air at all vinyl acetate exposure concentrations. With increasing the vinyl acetate exposure, concentration of acetaldehyde in expired air increased. At vinyl acetate exposure of approximately 1000 ppm the concentration of acetaldehyde in the expired air was 277 ppm (499 mg/cu m).
Rats were administered oral doses of 14C-vinyl acetate (labeled at the vinyl moiety, 1 mL of a 10000 ppm (v/v) aqueous solution, overall dose level 297 mg/kg bw) by gastric intubation. The dosing regimen was 6 times 1 hour apart. During the dosing regime and subsequent 96 hr collection period, a mean of 64.4% of the administered radioactivity was excreted (1.4% in feces, 1.8% in urine and 61.2% in exhaled air). In addition a mean of 5.4% was found in the carcass at 96 hr. The major portion of the urinary radioactivity was excreted within the first 24 hr. Most of the radioactivity eliminated by the expired air was recovered during the 6 hr dosing regime and the first 6 hr after dosing. This portion of radioactivity was recovered from the traps designed for collecting carbon dioxide. The authors of the study suppose, that the unaccounted 30.1% of the dose were most likely lost in the expired air, which escaped from the metabolism cages when the animals were removed for dosing. There was a wide tissue distribution of radioactivity following administration of 14C-vinyl acetate by the oral route. One hour after the sixth dose the highest mean concentrations of radioactivity were found in the harderian gland and the submaxillary salivary gland. High levels were also found in the liver, kidney, stomach, ileum, colon and gastrointestinal tract contents. Low concentrations of radioactivity were found in fat. Attempts have been undertaken to determine vinyl acetate metabolites in urine and feces. No radiolabeled carbonates or bicarbonates were found in urine or feces. Thin layer chromatography of urine indicated that there was one major radioactive fraction and several minor fractions. Exhaled radioactivity was entirely present as 14C carbon dioxide. Therefore it can be concluded, that 63 % of orally applied 14C vinyl acetate is excreted as metabolites.
For more Absorption, Distribution and Excretion (Complete) data for VINYL ACETATE (6 total), please visit the HSDB record page.
Vinyl acetate is primarily used as a monomer in the production of polyvinyl acetate and polyvinyl alcohol.
Used in the production of polyvinyl acetate emulsions, acrylic fiber, and polyvinyl alcohol; Occupational exposure occurs in production workers, painters, and floor layers; [ACGIH]
Painting (Solvents) [Category: Paint]
In polymerized form for plastic masses, films, and lacquers; in plastic form for food packaging; as a modifier for food starch
CHEMICAL INTERMEDIATE IN SYNTH OF POLYVINYL ACETATE EMULSIONS, RESINS & POLYVINYL ALCOHOL; INTERMEDIATE IN SYNTH OF OTHER POLYMERS, RESINS, AND EMULSIONS.
Safety glass interlayers
Typical /USA/ specifications are: ... acidity (as acetic acid), aldehydes (as acetaldehyde), 0.005% max, water, 0.04% max ...
In western Europe, vinyl acetate produced by the gas-phase ethylene process has the following typical specifications: ... ethyl acetate, 323 mg/kg (ppm): water, 240 mg/kg (ppm); methyl acetate, 175 mg/kg (ppm); acetaldehyde, 6 mg/kg (ppm); & acrolein, 1 mg/kg (ppm).
Typical specifications for vinyl acetate in Japan are as follows: ... free acid (as acetic acid), 0.01% max; free aldehydes (as acetaldehyde), 0.05% max ... moisture, 0.2% max ...
(1972) NEGLIGIBLE
(1975) 9.17X10+10 G
(1981) Exceeded 2.5x10+11 g
(1984) 2.34X10+11 g
(1987) 7.83X10+7
(1972) NEGLIGIBLE
(1975) 1.54X10+8 G
(1986) 1.16x10+7 lb
2023: 2,500,000,000 - <4,000,000,000 lb
(1972) 5.50X10+11 g
(1975) 5.86X10+11 g
(1984) 9.17X10+11 g
(1985) 2.11X10+9 lb
For more U.S. Production (Complete) data for VINYL ACETATE (21 total), please visit the HSDB record page.
60% FOR POLYVINYL ACETATE EMULSIONS AND RESINS; 15% FOR POLYVINYL ALCOHOL; 9% FOR VINYL CHLORIDE COPOLYMERS; 8% FOR POLYVINYL BUTYRAL; 3% FOR ETHYLENE-VINYL ACETATE RESINS AND EMULSIONS; 1% FOR POLYVINYL FORMAL; 4% FOR MISC APPLICATIONS AS A COPOLYMER (1971)
20% FOR ADHESIVE EMULSIONS; 17% FOR PAINT EMULSIONS; 12% FOR TEXTILE AND PAPER EMULSIONS; 23% FOR POLYVINYL ALCOHOL; 10% FOR ETHYLENE/VINYL/VINYL ACETATE; 8% FOR POLYVINYL BUTYRAL; 5% FOR POLYVINYL CHLORIDE COPOLYMERS; 5% FOR MISC (1984 EST)
CHEMICAL PROFILE: Vinyl acetate. Polyvinyl acetate emulsions and resins, 40%; (this area is divided evenly between paints and adhesives); polyvinyl alcohol, 15%; polyvinyl butyral, 8%; ethylene-vinyl acetate resins, 6%; polyvinyl chloride copolymers, 3%; miscellaneous, 1%; exports, 27%.
CHEMICAL PROFILE: Vinyl acetate. US Demand: 1988: 2.56 billion pounds; 1989: 2.62 billion pounds; 1993: 2.9 billion pounds /projected/ (Includes exports, but not imports, which averaged 6 million lb over the last three years.)
For more Consumption Patterns (Complete) data for VINYL ACETATE (13 total), please visit the HSDB record page.
Addition of acetic acid to acetylene ... in the gas phase in the presence of heterogeneous catalysts containing zinc salts.
Reaction of ethylene with acetic acid and oxygen ... in the gas phase on heterogeneous catalysts containing palladium.
REACTION OF ETHYLENE WITH SODIUM ACETATE
VINYL ACETATE CAN BE MADE BY REACTION OF GLACIAL ACETIC ACID & ACETYLENE IN PRESENCE OF MERCURY SALTS.
For more Methods of Manufacturing (Complete) data for VINYL ACETATE (9 total), please visit the HSDB record page.
Various commercial grades of vinyl acetate are available in USA, which differ only in the amt of inhibitor added: 3-5 mg/L (ppm) hydroquinone are present when use is expected within 2 mo of delivery; 14-17 mg/L (ppm) hydroquinone for up to 4 mo of storage; & 200-300 mg/L (ppm) diphenylamine when indefinite storage is anticipated.
GRADES OR PURITY: GRADE A (DIPHENYLAMINE-INHIBITED): 99.8%; GRADE H (HYDROQUINONE-INHIBITED): 99.8%
Cosmetics product ingredient: Vinyl acetate
Information on 41 consumer products that contain Vinyl acetate monomer in the following categories is provided:
Chemical Classes -> Nitrosamines/ethers/alcohols
Cosmetics -> Film forming
HistoryPolyvinyl acetate was discovered in Germany in 1912 by Fritz Klatte. The monomer, vinyl acetate, was first produced on an industrial scale by addition of acetic acid to acetylene with a mercury(I) salt[3] but it is now primarily made by palladium catalyzed oxidative addition of acetic acid to ethylene.
Verwendendrug delivery, hemodynamics, wound dressing, coatings
synthetischePVAc is a vinyl polymer. Polyvinyl acetate is prepared by polymerization of vinyl acetate monomer (free radical vinyl polymerization of the monomer vinyl acetate).
DefinitionChEBI: A polymer composed of repeating acetoxyethylene units.