Basic information
- Standard SMILES
C=C- InChIKey
VGGSQFUCUMXWEO-UHFFFAOYSA-N- Molecular formula
- C2H4
- Average molar mass
- 28.05 g/mol
Overview
Ethylene appears as a colorless gas with a sweet odor and taste. It is lighter than air. It is easily ignited and a flame can easily flash back to the source of the leak. Under prolonged exposure to fire or heat the containers may rupture violently and rocket. Can cause explosion.
Names & identifiers
- Preferred name
- Ethylene
- IUPAC
- ethene
- English name
- ethene
- Molecular formula
- C5H10
- Molecular weight
- 28.05
Names & synonyms
Show more names
Database identifiers
- CAS
56453-76-0- ChEMBL
CHEMBL117822- ChEBI
CHEBI:18153- UNII
- 91GW059KN7
- EC Number
- 200-815-3、682-561-7
- Nikkaji
- J1.671.339B、J1.939I
Properties
Computed structural properties
- XLogP
- 1.2
- Topological polar surface area
- 0 Ų
- Hydrogen bond donors
- 0
- Hydrogen bond acceptors
- 0
- Rotatable bonds
- 0
- Heavy atoms
- 2
- Formal charge
- 0
- Complexity
- 0
Experimental & physicochemical properties
Chemical Classes
Toxic Gases & Vapors -> Simple Asphyxiants
Flammable agents - 4th degree
Pesticides
Plant Growth Regulators
Active substance -> EU Pesticides database: Approved
LogP
log Kow = 1.13
1.13
1.13
Odor
Sweet
Olefinic, hedonic tone: unpleasant to neutral
Taste
Tasteless
Sweet
Density
0.569 at -154.84 °F (USCG, 1999) - Less dense than water; will float
Density: 50.5678 g/cu cm at -104 °C
0.569 at -154.84 °F
0.568 @ -104°C
Solubility
In water, 131 mg/L at 25 °C
Slightly soluble in water
1 volume dissolves in about 4 volumes water at 0 °C, in about 9 volumes water at 25 °C, in about 0.5 volumes alcohol at 25 °C, in about 0.05 volumes ether at 15.5 °C
Very soluble in ethanol, ether; soluble in acetone acid, benzene
Soluble in acetone, benzene
0.131 mg/mL at 25 °C
Flash Point
-213 °F (approx.) (USCG, 1999)
-213 °F
-100 °C (-148 °F) - closed cup
Flammable gas
-213 °F (approx)
Physicochemical properties
- Melting point
- 146.8 °C · 146.8 °C
- Density
- 0.8997 g/cm3 · 0.8997 g/cm3
- pka
- 44 · 44(at 25℃)
- EPA Substance Registry System
- 1 · 1-Propene, polymer with ethene, isotactic (56453-76-0)
- TSCA
- TSCA listed
Safety & regulation
GHS classification
GHS Classification
Danger
H220: Extremely flammable gas [Danger Flammable gases]
P203, P210, P222, P261, P271, P280, P304+P340, P319, P377, P381, P403, P403+P233, P405, and P501 (click each P-code to see the statement)
This chemical does not meet GHS hazard criteria for 0.8% (38 of 4869) of reports.
Danger
H220 (99.2%): Extremely flammable gas [Danger Flammable gases]
Hazard information
Regulatory Information
Chemical: Ethene
Regulation (EC) No 1935/2004 (amended)
Ethene is listed on the EPA's Chemical Data Reporting (CDR) system. Manufacturers and importers of Ethene 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)
Reg. (EU) 2022/708, 2008/127/EC, Reg. (EU) 2017/195, Reg. (EU) 2018/155, Reg. (EU) 2023/1446, Reg. (EU) No 187/2013, Reg. (EU) No 540/2011
Status: Active Update: 17-05-2023 https://echa.europa.eu/registration-dossier/-/registered-dossier/16094
Ethene (ethylene): HSNO Approval: HSR001001 Approved with controls
DOT Label
Flammable Gas
Flammable Gas
Fire Hazards
Special Hazards of Combustion Products: Vapors are anesthetic.
Excerpt from ERG Guide 115 [Gases - Flammable (Including Refrigerated Liquids)]:
· EXTREMELY FLAMMABLE.
· EXTREMELY FLAMMABLE.
Extremely flammable. Gas/air mixtures are explosive.
Fire Potential
A highly flammable gas ... .
A very dangerous fire hazard when exposed to heat or flame.
Health Hazards
Moderate concentration in air causes drowsiness, dizziness, and unconsciousness. Overexposure causes headache, drowsiness, muscular weakness. (USCG, 1999)
Excerpt from ERG Guide 115 [Gases - Flammable (Including Refrigerated Liquids)]:
· Vapors may cause dizziness or asphyxiation without warning, especially when in closed or confined areas.
· Vapors may cause dizziness or asphyxiation without warning, especially when in closed or confined areas.
Hazards Summary
Inhalation of high concentrations cause CNS depression and anesthesia; [Merck Index] Simple asphyxiant; Inhalation of high concentrations can cause CNS depression; [ICSC] Ethylene, compressed (UN1962) has warning of explosive polymerization; [ERG 2016]
DOT ID and Guide
1038 115
1962 116P
Reactive Group
Hydrocarbons, Aliphatic Unsaturated
Hydrocarbons, Aliphatic Unsaturated
Special Reports
USEPA/Office of Prevention, Pesticides and Toxic Substances; Reregistration Eligibility Decision Document - Ethylene (September 1992). The RED summarizes the risk assessment conclusions and outlines any risk reduction measures necessary for the pesticide to continue to be registered in the USA.[Available from, as of June 28, 2017: http://www.epa.gov/pesticides/reregistration/status.htm]
OECD; Screening Information Data Set for Ethylene, 74-85-1 (October 1998).[Available from, as of July 28, 2017: http://www.inchem.org/documents/sids/sids/74851.pdf]
FIFRA Requirements
Ethylene is exempted from the requirement of a tolerance for residues when: (a) For all food commodities, it is used as a plant regulator on plants, seeds, or cuttings and on all food commodities after harvest and when applied in accordance with good agricultural practices. (b) Injected into the soil to cause premature germination of witchweed in bean (lima and string), cabbage, cantaloupe, collard, corn, cotton, cucumber, eggplant, okra, onion, pasture grass, pea (field and sweet), peanut, pepper, potato, sweet potato, sorghum, soybean, squash, tomato, turnip, and watermelon fields as part of the U.S. Department of Agriculture witchweed control program.
Section 4(g)(2)(A) of FIFRA requires the Agency to determine, after submission of relevant data concerning an active ingredient, whether products containing the active ingredient are eligible for reregistration. The Agency has waived all generic (ie, active ingredient specific) data requirements except for technical chemistry data and additionally has relied on public literature for mammalian toxicology. The Agency has completed its review of this information data and other factors and considerations, and has determined this information is sufficient to support reregistration of all products containing ethylene for all uses. ... The Agency therefore finds that products containing only ethylene as an active ingredient are eligible for reregistration and may be reregistered once the confidential statements of formula and amended labeling are received and accepted by the Agency.
As the federal pesticide law FIFRA directs, EPA is conducting a comprehensive review of older pesticides to consider their health and environmental effects and make decisions about their continued use. Under this pesticide reregistration program, EPA examines newer health and safety data for pesticide active ingredients initially registered before November 1, 1984, and determines whether the use of the pesticide does not pose unreasonable risk in accordance to newer safety standards, such as those described in the Food Quality Protection Act of 1996. Pesticides for which EPA had not issued Registration Standards prior to the effective date of FIFRA '88 were divided into three lists based upon their potential for human exposure and other factors, with List B containing pesticides of greater concern than those on List C, and with List C containing pesticides of greater concern than those on List D. Ethylene is found on List C. Case No: 3071; Pesticide type: herbicide; Case Status: RED Approved 09/92; OPP has made a decision that some/all uses of the pesticide are eligible for reregistration, as reflected in a Reregistration Eligibility Decision (RED) document.; Active ingredient (AI): ethylene; AI Status: OPP has completed a Reregistration Eligibility Decision (RED) for the case/AI..
Safety & protection
Fire Fighting
Excerpt from ERG Guide 116 [Gases - Flammable (Unstable); polymerization hazard]:
Excerpt from ERG Guide 115 [Gases - Flammable (Including Refrigerated Liquids)]:
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. Combat fire from a sheltered position.
Accidental Release Measures
· 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.
· 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.
First Aid
Remove victim to fresh air, give artificial respiration and oxygen if breathing has stopped, and call a physician. (USCG, 1999)
Excerpt from ERG Guide 115 [Gases - Flammable (Including Refrigerated Liquids)]:
General First Aid:
General First Aid:
Exposure Control and Personal Protection
· Wear positive pressure self-contained breathing apparatus (SCBA).
· Wear positive pressure self-contained breathing apparatus (SCBA).
Fire Fighting Procedures
Suitable extinguishing media: Use water spray, alcohol-resistant foam, dry chemical or carbon dioxide.
Advice for firefighters: Wear self-contained breathing apparatus for firefighting if necessary.
To fight fire, stop flow of gas, use CO2, dry chemical, or fine water spray.
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 quantities of water. Apply water from as far a distance as possible. /Ethylene, compressed; ethylene, refrigerated liquid/
For more Fire Fighting Procedures (Complete) data for Ethylene (6 total), please visit the HSDB record page.
Storage Conditions
Store in cool dry, well-ventilated location. Protect against static electricity and lightning. Isolate from oxidizing materials, halogens, and other combustibles.
Keep container tightly closed in a dry and well-ventilated place. Contents under pressure. Storage class (TRGS 510): Gases
Protect containers against physical damage. Outdoor or detached storage is preferred. For indoor storage, use a fireproof, well-ventilated, area isolated from any sources of ignition.
Cleanup Methods
ACCIDENTAL RELEASE MEASURES: Personal precautions, protective equipment and emergency procedures. Use personal protective equipment. Avoid breathing vapors, mist or gas. Ensure adequate ventilation. Remove all sources of ignition. Evacuate personnel to safe areas. Beware of vapors accumulating to form explosive concentrations. Vapors can accumulate in low areas. Environmental precautions: Prevent further leakage or spillage if safe to do so. Do not let product enter drains. Methods and materials for containment and cleaning up: Clean up promptly by sweeping or vacuum.
Spills on water: Contain if possible. If solubilized in water, apply activated carbon at 10% of the spill amount over the region occupied by 10 mg/L or greater concentrations. Mechanical dredges or lifts may then be used to remove immobilized masses of pollutants. Peat moss is also recommended as a sorbent.
By forced ventilation, maintain concentration of gas below the range of explosive mixture. Remove the tank or cylinder to an open area. Leave to bleed off in the atmosphere.
Evacuate danger area! Ventilation. Remove all ignition sources and turn off gas at source if possible. Personal protection: chemical protection suit including self-contained breathing apparatus.
Nonfire Spill Response
Excerpt from ERG Guide 116 [Gases - Flammable (Unstable); polymerization hazard]:
Excerpt from ERG Guide 115 [Gases - Flammable (Including Refrigerated Liquids)]:
Disposal Methods
SRP: 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 air, soil or water; effects on animal, aquatic and plant life; and conformance with environmental and public health regulations. If it is possible or reasonable use an alternative chemical product with less inherent propensity for occupational harm/injury/toxicity or environmental contamination.
Product: Burn in a chemical incinerator equipped with an afterburner and scrubber but exert extra care in igniting as this material is highly flammable. Offer surplus and non-recyclable solutions to a licensed disposal company. Contact a licensed professional waste disposal service to dispose of this material. Contaminated packaging: Dispose of as unused product.
Do not discharge ethylene directly into sewers or surface waters. Dispose of by incineration. If necessary, a flammable solvent may be added to aid in burning.
Toxicology
Environmental Fate
TERRESTRIAL FATE: Based on a classification scheme(1), an estimated Koc value of 13(SRC), determined from a structure estimation method(2), indicates that ethylene is expected to have very high mobility in soil(SRC). Volatilization of ethylene from moist soil surfaces is expected to be an important fate process(SRC) given a Henry's Law constant of 0.228 atm-cu m/mole(3). Ethylene is expected to volatilize from dry soil surfaces(SRC) based upon a vapor pressure of 5.21X10+4 mm Hg at 25 °C(4). Biodegradation data in soil were not available(SRC, 2017). However, ethylene was biodegraded to ethylene oxide using acclimated cell free extracts(8).
AQUATIC FATE: Based on a classification scheme(1), an estimated Koc value of 13(SRC), determined from a structure estimation method(2), indicates that is not expected to adsorb to suspended solids and sediment(SRC). Volatilization from water surfaces is expected(3) based upon a Henry's Law constant of 0.228 atm-cu m/mole(4). Using this Henry's Law constant and an estimation method(3), volatilization half-lives for a model river and model lake are 2 hrs and 2 days, respectively(SRC). According to a classification scheme(5), an estimated BCF of 2.6(SRC), from its log Kow of 1.13(6) and a regression-derived equation(2), suggests the potential for bioconcentration in aquatic organisms is low(SRC). Biodegradation data in water were not available(SRC, 2017). However, ethylene was biodegraded to ethylene oxide using acclimated cell free extracts(7).
ATMOSPHERIC FATE: According to a model of gas/particle partitioning of semivolatile organic compounds in the atmosphere(1), ethylene, which has a vapor pressure of 5.21X10+4 mm Hg at 25 °C(2), is expected to exist solely as a gas in the ambient atmosphere. Gas-phase ethylene 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 2 days(SRC), calculated from its rate constant of 7.9X10-12 cu cm/molecule-sec at 25 °C(3). Gas-phase ethylene will also be degraded in the atmosphere by reaction with ozone and nitrate radicals with respective half-lives of 6.5 and 190 days(4-6). Ethylene absorbs UV at wavelength 175.2 nm(7) and, therefore, is not expected to be susceptible to direct photolysis by sunlight since sunlight consists of wavelengths above 290 nm(SRC).
Food Survey Values
Ethylene was detected at concentrations of 2.27 and 9.32 uL/L in internal samples of Bisbee Delicious apples from 2 orchards during fruit growth and maturation in 1990(1). Ethylene has been found in the gaseous metabolites released by germinating bean, corn, cotton, and pea seeds(2).
Toxicity Summary
IDENTIFICATION AND USE: Ethylene is a colorless gas. It is used for oxyethylene welding and cutting metals, as well as in the manufacture of alcohol, mustard gas, and many other organics. It is also used in manufacture of ethylene oxide (for plastics), polythene, polystyrene and other plastics. Ethylene is a plant growth regulator, which is used commercially to accelerate the ripening of various fruits. HUMAN STUDIES: Exposure to 37.5% ethylene for 15 min may result in marked memory disturbances. Humans exposed to as much as 50% ethylene in air, whereby the oxygen availability is decreased to 10%, experienced a loss of consciousness. Prolonged inhalation of 85% ethene in air is slightly toxic, whereas 94% in oxygen is fatal. Death is certain at 8% oxygen. In fatal human intoxication, ethylene affects the respiratory center of the brain and kills by suffocation. Postmortem analysis has revealed that the right side of the heart is full of blood, while the left side is empty. In workers chronically exposed, ethylene has been associated with a decrease in maximum arterial pressure, slower pulse, lengthened later period of the visual-motor response, increased thresholds of olfaction and hearing, and tension of the thermoregulatory apparatus. In eight people not occupationally exposed to ethylene, the DNA adduct 7-(2-hydroxyethyl)guanine was detected at a background level in peripheral lymphocytes. ANIMAL STUDIES: Mice were dosed by gavage with 3.75 mg/kg bw ethylene for 4 months. The treated animals displayed no changes in behavior or in body weight gain and oxygen consumption. Gross pathology examination revealed no changes in the relative weights or in the histological structure of the visceral organs. Inhalation exposure to 600,000 ppm continuously for 90 days in rats caused reduced food uptake and activity, peripheral leucopenia, decreased thrombocyte and erythrocyte count, and decrease in bone marrow cellularity. One-day-old and adult rats continuously exposed to 3 mg/cu m per day for 90 days exhibited hypertension, disruption of the subordination chronaxy, and decreased cholinesterase activity. Experiments proved ethylene to be metabolized in certain species, notably mice and rats, into the carcinogenic and mutagenic ethylene oxide. Administration of ethylene by head-only exposure revealed no potential for adverse reproductive effects in the rat. Ethylene was not found to be mutagenic with or without metabolic activation in Salmonella typhimurium strains TA98, TA1537, TA100, or TA1535. Rats and mice exposed 6 hr/day 5 days/week for 4 weeks to 40-3000 ppm ethylene did not have a significant increase in the frequency of micronucleated polychromatic erythrocytes in the bone marrow, when compared to the control group.
Ecotoxicity Excerpts
/PLANTS/ Incubation of cut spurs of Hippophae rhamnoides in atmospheres containing 1 mL ethylene/L for 120 hr induced formation of abscission layer and complete abscission of ripe fruit within 1 week. Presence of leaves decreased the abscisic effect of ethylene.
/PLANTS/ Treating potato tubers with ethylene donors (Hydrel, Dihydrol or Camposan) inhibited the sprouting of the growth points and increased abscisic acid content of the meristem of the growth points and of the cortical parenchyma. However, abscisic acid content of the tubers increased less when Hydrel was used at growth-stimulating (0.05%) than at growth-inhibiting (0.5 and 1%) concentrations. Abscisic acid concentration in the tubers decreased 90-120 days after the treatment resulting in active tuber sprouting after that time when 0.05% Hydrel was used, while when the high Hydrel concentrations were applied, the abscisic acid concentration remained still at a high level inhibiting the sprouting 120-150 days after treatment and even later. Thus, the increase in abscisic acid concentration resulting from treatment with ethylene donors was the main cause of inhibition of tuber sprouting. The other ethylene donors behaved similarly as Hydrel did also increasing the abscisic acid concentration in the tuber tissues. In the control tubers (treated with 0.05% ethylene donors) the abscisic acid decreased 210 days after the treatment to 0.08 ug/g fresh matter while in tubers treated at 0.5% concentration it remained at that time at a level 10-fold that in the control. A direct relation between the concentration of ethylene donors used for treatment and abscisic acid concentration in the tubers was found.
/PLANTS/ Easter lilies (Lilium longiflorum) were treated with ethylene or ethephon at several development stages of flower buds. Ethylene hastened flower-bud opening. The earlier ethylene treatment during the flower-bud development stages, the earlier flowering occurred. Ethylene or ethephon treatment decreased tepal length, but increased degenerated flower buds and distorted flowers. Ethylene also hastened flower senescence to result in earlier wilting and earlier dropping of flowers.
/PLANTS/ Malformation is arguably the most crucial disease of mango (Mangifera indica L.). The etiology of the disease has not yet been successfully resolved. Here, we quantified the endogenous ethylene content in malformed and healthy vegetative and floral tissues of mango cultivars viz., Amrapali, Bombay green, Chausa, Dushehri and Mallika. Levels of ethylene were higher in malformed vegetative and floral tissues as compared with that of healthy tissues at both prior to full bloom and full bloom stages. The study also revealed that isolates of Fusarium dissected from mango exhibited most morphological similarities to the accepted standard features of Fusarium mangiferae. The growth dynamic of F. mangiferae were evaluated with varying temperatures ranging from 5 to 40 °C. Temperatures of 25 °C, 30 °C and 35 °C were better suited for growth of F. mangiferae than temperatures of 20 °C or 40 °C. Conidium germination of F. mangiferae was maximum at 30 °C and minimum at <15 °C. World-wide occurrence of mango malformation showed its most severity at 10-15 °C temperature range. Stress ethylene level is higher in diseased tissue at the same temperature range where growth of Fusaria is found to be completely restricted. The present study provides direct evidence that low temperature induced 'stress ethylene' is potentially responsible for the disease while on the other hand Fusarium role in the disease either through toxic principle or malformation inducing principle is not conclusive at <15 °C and is rather out of question.
/PLANTS/ Regulation of stomatal aperture is crucial in terrestrial plants for controlling water loss and gaseous exchange with environment. While much is known of signaling for stomatal opening induced by blue light and the role of hormones, little is known about the regulation of stomatal closing in darkness. The present study was aimed to verify their role in stomatal regulation in darkness. Epidermal peelings from the leaves of Commelina benghalensis were incubated in a defined medium in darkness for 1 hr followed by a 1 hr incubation in different test solutions [hydrogen peroxide, propyl gallate, ethrel (ethylene), silver nitrate, sodium orthovanadate, tetraethyl ammonium chloride, calcium chloride, lanthanum chloride, separately and in combination] before stomatal apertures were measured under the microscope. In the dark stomata remained closed under treatments with ethylene and propyl gallate but opened widely in the presence of hydrogen peroxide and silver nitrate. The opening effect was largely unaffected by supplementing the treatment with Na-vanadate (PM H+ ATPase inhibitor) and tetraethyl ammonium chloride (K(+)-channel inhibitor) except that opening was significantly inhibited by the latter in presence of hydrogen peroxide. On the other hand, hydrogen peroxide could not override the closing effect of ethylene at any concentrations while a marginal opening of stomata was found when silver nitrate treatment was given together with propyl gallate. Calcium chloride treatment opened stomata in the darkness while lanthanum chloride maintained stomata closed. A combination of lanthanum chloride and propyl gallate strongly promoted stomatal opening. A probable action of ethylene in closing stomata of Commelina benghalensis in dark has been proposed.
Ongoing Test Status
The following link will take the user to the National Toxicology Program (NTP) Test Status of Agents Search page, which tabulates the results and current status of tests such as "Short-Term Toxicity Studies", "Long-term Carcinogenicity Studies", "Developmental Studies", "Genetic Toxicology Studies", etc., performed with this chemical. Testing status for ethylene is available.[Available from, as of July 26, 2017: https://ntpsearch.niehs.nih.gov/?e=True&ContentType=Testing+Status]
Regulatory information
FIFRA Requirements
Ethylene is exempted from the requirement of a tolerance for residues when: (a) For all food commodities, it is used as a plant regulator on plants, seeds, or cuttings and on all food commodities after harvest and when applied in accordance with good agricultural practices. (b) Injected into the soil to cause premature germination of witchweed in bean (lima and string), cabbage, cantaloupe, collard, corn, cotton, cucumber, eggplant, okra, onion, pasture grass, pea (field and sweet), peanut, pepper, potato, sweet potato, sorghum, soybean, squash, tomato, turnip, and watermelon fields as part of the U.S. Department of Agriculture witchweed control program.
Section 4(g)(2)(A) of FIFRA requires the Agency to determine, after submission of relevant data concerning an active ingredient, whether products containing the active ingredient are eligible for reregistration. The Agency has waived all generic (ie, active ingredient specific) data requirements except for technical chemistry data and additionally has relied on public literature for mammalian toxicology. The Agency has completed its review of this information data and other factors and considerations, and has determined this information is sufficient to support reregistration of all products containing ethylene for all uses. ... The Agency therefore finds that products containing only ethylene as an active ingredient are eligible for reregistration and may be reregistered once the confidential statements of formula and amended labeling are received and accepted by the Agency.
As the federal pesticide law FIFRA directs, EPA is conducting a comprehensive review of older pesticides to consider their health and environmental effects and make decisions about their continued use. Under this pesticide reregistration program, EPA examines newer health and safety data for pesticide active ingredients initially registered before November 1, 1984, and determines whether the use of the pesticide does not pose unreasonable risk in accordance to newer safety standards, such as those described in the Food Quality Protection Act of 1996. Pesticides for which EPA had not issued Registration Standards prior to the effective date of FIFRA '88 were divided into three lists based upon their potential for human exposure and other factors, with List B containing pesticides of greater concern than those on List C, and with List C containing pesticides of greater concern than those on List D. Ethylene is found on List C. Case No: 3071; Pesticide type: herbicide; Case Status: RED Approved 09/92; OPP has made a decision that some/all uses of the pesticide are eligible for reregistration, as reflected in a Reregistration Eligibility Decision (RED) document.; Active ingredient (AI): ethylene; AI Status: OPP has completed a Reregistration Eligibility Decision (RED) for the case/AI..
Atmospheric Standards
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. Ethylene is produced, as an intermediate or a final product, by process units covered under this subpart.
DHS Chemicals of Interest (COI)
Ethylene
1
10000
Flammable chemical that can be released at a facility.
Safety data
- tsca
- TSCA listed
Chemistry & industry
Pharmacology
Metabolism/Metabolites
Rat liver microsomal monooxygenases transform ethylene to oxirane. ...
Male CBA mice exposed to air containing 19.6 mg/cu m ... (14)C-labeled ethylene metabolized ethylene to ethylene oxide, which binds to cellular proteins.
Four male CBA mice (average body weight, 31 g) were exposed together for 1 hr in a closed glass chamber (5.6 L) to (14)C-ethylene (22 mCi/mmol) in air at 17 ppm x hr (22.3 (mg/cu m) x hr, equivalent to about 1 mg/kg bw). Blood and organs from two mice were pooled 4 hr after the end of exposure. Radioactivity was about the same in kidney (0.16 uCi/g wet weight) and liver (0.14 uCi/g) but lower in testis (0.035 uCi/g), brain (0.02 uCi/g) and Hb (0.0094 uCi/g Hb). Urine was collected from the two other mice during 48 hr, and blood was collected after 21 days. 5-(2-Hydroxyethyl)cysteine was identified as a metabolite of ethylene in urine (3% of (14)C in urine) by thin-layer chromatography. The radioactivity in Hb was 0.011 uCi/g Hb. These data, together with those on specific hydroxyethyl derivatives at amino acid residues of Hb, indicated that ethylene was metabolized to ethylene oxide.
Experiments proved ethylene to be converted in certain species, notably mice and rats, into the carcinogenic and mutagenic ethylene oxide. Carcinogenic effect of ethylene of endogenous origin is suggested. Whether such an effect is possible with oral administration of ethylene is not clear.
Absorption, Distribution and Excretion
When equilibrium is reached, the rate of transfer of gas molecules from the alveolar space to blood equals the rate of removal by blood from the alveolar space. For example, ... ethylene has a low (0.14) blood/gas phase solubility ratio. For a substance with a low solubility ratio such as ethylene, only a small percentage of the total gas is removed by blood during each circulation because blood is soon saturated with the gas.
Ethylene has been determined in expired air of 2/8 human subjects at rate of 0.91 and 120 ug/hr.
... Excreted in urine ...
The inhalation pharmacokinetics of ethylene have been investigated in human volunteers at atmospheric concentrations of up to 50 ppm (157.5 mg/cu m) by gas uptake in a closed spirometer system. The uptake, exhalation and metabolism of ethylene can be described by first-order kinetics. Uptake of ethylene into the body is low. Clearance due to uptake, which reflects the transfer rate of ethylene from the atmosphere into the body, was 25 L/hr for a man of 70 kg. This value represents only 5.6% of the experimentally obtained alveolar ventilation rate of 150 L/hr. The majority (94.4%) of ethylene inhaled into the lungs is exhaled again without becoming systemically available via the blood stream. Maximal accumulation of ethylene in the same man, determined as the thermodynamic partition coefficient whole body:air was 0.53. The concentration ratio at steady state was even smaller (0.33), owing to metabolic elimination. Clearance due to metabolism, in relation to the concentration in the atmosphere, was calculated to be 9.3 L/hr for a man of 70 kg. This indicates that at steady state about 36% of systemically available ethylene is eliminated metabolically and 64% is eliminated by exhalation as the unchanged substance, as can be calculated from the values of clearance of uptake and of clearance of metabolism. The biological half-life of ethylene was 0.65 hr. The alveolar retention of ethylene at steady state was calculated to be 2%. From theoretical considerations of the lung uptake of gases and vapors, it can be deduced that the low uptake rate of ethylene is due to its low solubility in blood: Ostwald's solubility coefficient for human blood at 37 °C, 0.15.
For more Absorption, Distribution and Excretion (Complete) data for Ethylene (8 total), please visit the HSDB record page.
Uses & manufacturing
Uses
Used in oxyethylene welding, chemical manufacturing, fruit ripening; Has been used as a general anesthetic; [Merck Index]
Gas Welding and Cutting [Category: Weld]
For ethylene (USEPA/OPP Pesticide Code: 041901) ACTIVE products with label matches. /SRP: Registered for use in the U.S. but approved pesticide uses may change periodically and so federal, state and local authorities must be consulted for currently approved uses./
Oxyethylene welding and cutting metals; manufacture of alcohol, mustard gas, and many other organics. Manufacture of ethylene oxide (for plastics), polythene, polystyrene and other plastics. Plant growth regulator; used commercially to accelerate the ripening of various fruits.
Induces ripening; causes leaves to droop and drop; promotes senescence.
Ethylene is used in the production of fabricated plastics, antifreeze; making fibers; to manufacture ethylene oxide, polyethylene for plastics, alcohol, mustard gas, and other organics.
Impurities
Purity not less than 96% ethylene by gas volume, not more than 0.5% acetylene, not more than 4% methane and ethane.
Sulfur, oxygen, acetylene, hydrogen, carbon monoxide and carbon dioxide are the most troublesome and carefully controlled impurities, especially when ethylene from multiple sources is mixed in transportation.
U.S. Exports
(1972) NEGLIGIBLE
(1975) 1.41X10+9 GRAMS
Exports rose from barely 1 million pounds in 1991 to over 35 million pounds in 1992.
U.S. Imports
(1972) NEGLIGIBLE
(1984) 1.50X10+9 g
Imports grew from 20 million pounds in 1991 to 95 million pounds in 1992.
U.S. Production
2023: 75,000,000,000 - <80,000,000,000 lb
(1972) 9.47X10+12 GRAMS
(1975) 9.31X10+12 GRAMS
(1985) 1.39X10+12 g
(1990) 36.47 billion lb
For more U.S. Production (Complete) data for Ethylene (15 total), please visit the HSDB record page.
Consumption Patterns
40.5% FOR POLYETHYLENE; 19.5% FOR ETHYLENE OXIDE; 14% FOR ETHYLENE DICHLORIDE; 8.5% FOR ETHYLBENZENE; 5.5% FOR ETHYL ALCOHOL; 4% FOR ACETALDEHYDE; 2% FOR LINEAR PRIMARY ALCOHOLS; 2% FOR VINYL ACETATE MONOMER; 4% FOR MISC APPLICATIONS (1973)
... LESS THAN 0.5 MILLION KG ETHYLENE ARE USED ANNUALLY TO RIPEN FRUITS & VEGETABLES.
Polyethylene resins, 48%; Ethylene oxide, 18%; Ethylene dichloride, 13%; Ethylbenzene, 8%; Linear alcohols, 5%; Vinyl Acetate, 2%; Ethyl alcohol, 2%; Miscellaneous, 4% (1984)
CHEMICAL PROFILE: Ethylene. Low-density polyethylene (including linear low-density polyethylene), 28%; high-density polyethylene, 24%; ethylene oxide, 14.8%; ethylene dichloride, 12.3%; ethylbenzene, 8%; linear olefins and alcohols, 6%; vinyl acetate monomer, 2.6%; acetaldehyde, 1.3%; ethyl alcohol, 1%; ethylene-propylene elastomers, 1%; miscellaneous, 1%.
For more Consumption Patterns (Complete) data for Ethylene (8 total), please visit the HSDB record page.
Methods of Manufacturing
... Production of ethylene is currently based on steam cracking of petroleum hydrocarbons. Various feedstocks, including ethane, propane, butanes, naphthas and gas oils, are used to produce ethylene. Naphthas are the principal raw material used in western Europe and Japan, accounting for over 80% of the ethylene produced. Ethane is the primary feedstock in the USA, followed by propane, naphthas, gas oils and butane. Small amounts of ethylene are recovered from other feedstocks, such as retrograde-field condensates and refinery waste gases. Dehydration of ethanol is the third commercial route to ethylene.
Prepared by decomposition of petroleum gases or by dehydration of alcohol.
The bulk of the worldwide annual commercial production of ethylene is based on thermal cracking of petroleum hydrocarbons with steam; the process is commonly called pyrolysis or steam cracking.
Although ethylene is produced by various methods as follows, only a few are commercially proven: thermal cracking of hydrocarbons /the principal route for the industrial production of ethylene/, catalytic pyrolysis, membrane dehydrogenation of ethane, oxydehydrogenation of ethane, oxidative coupling of methane, methanol to ethylene, dehydration of ethanol, ethylene from coal, disproportionation of propylene, and ethylene as a by-product.
Formulations/Preparations
Banana Gas - 32 (Praxair Distribution, Inc): Active ingredient: ethylene 6.3%.
Liquid Ethylene Technical Grade (Eastman Chemical Company): Active ingredient: ethylene 99.97%.
Livingston's Tobacco Curing Gas (Livingston Group, Inc): Active ingredient: ethylene 99.9%.
Livingston's Nature-Ripe (Livingston Group, Inc): Active ingredient: ethylene 99.9%.
For more Formulations/Preparations (Complete) data for Ethylene (11 total), please visit the HSDB record page.
General Manufacturing Information
All Other Basic Organic Chemical Manufacturing
Ethene: ACTIVE
Ethylene quality worldwide is matched to customer requirements; no single chemical-grade ethylene exists. However, ethylene content normally exceeds 99.9 wt%. The reason for variation in ethylene specifications is due to the use of ethylene in downstream processes that differ in sensitivity to impurities in ethylene, due to different catalyst systems being used.
Suppliers1 total
Additional notes
DefinitionA gaseous alkene. Ethene is not normally present in the gaseous fraction of crude oil but can be obtained from heavier fractions by catalytic cracking. This is the principal industrial source. The compound is important as a starting material in the organic-chemicals industry (e.g. in the manufacture of ethanol) and as the starting material for the production of polyethene. Ethene is the first member of the homologous series of alkenes.
Related reactions
No reaction records under the current filter.
Linked notes
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