1,2-Dibromoethene
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1,2-Dibromoethene
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CAS No:
540-49-8
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Formula:
C2H2Br2
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Chemical Name:
1,2-Dibromoethene
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Synonyms:
Ethene,1,2-dibromo-;Ethylene,1,2-dibromo-;1,2-Dibromoethene;1,2-Dibromoethylene;Acetylene dibromide;sym-Dibromoethylene;2-Bromovinyl bromide;NSC 8744
- Categories:
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CAS No:
1,2-Dibromoethene Basic Attributes
185.85
185.85
208-747-6
DTXSID3060241
Colorless liquid
2903399090
Characteristics
0 Ų
2.24740
2.21 g/cm3 @ Temp: 17 °C
-53 °C
110 °C @ Press: 754 Torr
n20/D 1.542
0.03 M
31.00 mmHg
MP: -53 °C; BP: 112.5 °C @ 760 MM HG; DENSITY: 2.2464 @ 20 °C; SOL IN ALC, ETHER, ACETONE, BENZENE & CHLOROFORM /CIS-FORM/|MS: 1250 (Atlas of Mass Spectral Data, John Wiley & Sons, New York) /Ethylene, 1,2-dibromo (cis)/|MS: 1250 (Atlas of Mass Spectral Data, John Wiley & Sons, New York) /Ethylene, 1,2-dibromo (trans)/
Corrosive
Safety Information
III
6.1(b)
UN 2810 6.1/PG 3
3
25-36/37/38
26-36/37/39-45
KV7700000
T
LIQUID, GRADUALLY DECOMPOSED BY AIR, MOISTURE, OR LIGHT
P261-P301 + P310-P305 + P351 + P338
H301-H315-H319-H335
SRP: At the time of review, criteria for land treatment or burial (sanitary landfill) disposal practices are subject to significant revision. Prior to implementing land disposal of waste residue (including waste sludge), consult with environmental regulatory agencies for guidance on acceptable disposal practices.
ITC/USEPA; Information Review #211 (Draft) 1,2-Dibromoethene (1980).
|Danger|H301 (100%): Toxic if swallowed [Danger Acute toxicity, oral]|P261, P264, P270, P271, P280, P301+P310, P302+P352, P304+P340, P305+P351+P338, P312, P321, P330, P332+P313, P337+P313, P362, P403+P233, P405, and P501|Aggregated GHS information provided by 43 companies from 4 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
Explosions may occur during distillation of bromoacetylenes when bath temperatures are too high, or if air is admitted to a hot vacuum-distillation residue. /Bromoacetylenes/
Haloacetylenes should be used with exceptional precautions. /Haloacetylenes/
If ... THERE IS NO FIRE, go directly to the Table of Initial Isolation and Protective Action Distances /(see table below)/ ... to obtain initial isolation and protective action distances. IF THERE IS A FIRE, or IF A FIRE IS INVOLVED, go directly to the appropriate guide /(see guide(s) below)/ and use the evacuation information shown under PUBLIC SAFETY.|/GUIDE 154: SUBSTANCES - TOXIC AND/OR CORROSIVE (NON-COMBUSTIBLE)/ Health: TOXIC; inhalation, ingestion, or skin contact with material may cause severe injury or death. Contact with molten substance may cause severe burns to skin and eyes. Avoid any skin contact. Effects of contact or inhalation may be delayed. Fire may produce irritating, corrosive and/or toxic gases. Runoff from fire control or dilution water may be corrosive and/or toxic and cause pollution.|/GUIDE 154: SUBSTANCES - TOXIC AND/OR CORROSIVE (NON-COMBUSTIBLE)/ Fire or Explosion: Non-combustible, substance itself does not burn but may decompose upon heating to produce corrosive and/or toxic fumes. Some are oxidizers and may ignite combustibles (wood, paper, oil, clothing, etc.). Contact with metals may evolve flammable hydrogen gas. Containers may explode when heated.|/GUIDE 154: SUBSTANCES - TOXIC AND/OR CORROSIVE (NON-COMBUSTIBLE)/ Public Safety: CALL Emergency Response Telephone Number ... . As an immediate precautionary measure, isolate spill or leak area in all directions for at least 50 meters (150 feet) for liquids and at least 25 meters (75 feet) for solids. Keep unauthorized personnel away. Stay upwind. Keep out of low areas. Ventilate enclosed areas.|For more DOT Emergency Guidelines (Complete) data for 1,2-DIBROMOETHYLENE (9 total), please visit the HSDB record page.
No person may /transport,/ offer or accept a hazardous material for transportation in commerce unless that person is registered in conformance ... and the hazardous material is properly classed, described, packaged, marked, labeled, and in condition for shipment as required or authorized by ... /the hazardous materials regulations (49 CFR 171-177)./|The International Air Transport Association (IATA) Dangerous Goods Regulations are published by the IATA Dangerous Goods Board pursuant to IATA Resolutions 618 and 619 and constitute a manual of industry carrier regulations to be followed by all IATA Member airlines when transporting hazardous materials.|The International Maritime Dangerous Goods Code lays down basic principles for transporting hazardous chemicals. Detailed recommendations for individual substances and a number of recommendations for good practice are included in the classes dealing with such substances. A general index of technical names has also been compiled. This index should always be consulted when attempting to locate the appropriate procedures to be used when shipping any substance or article.
1,2-Dibromoethylene is a lachrymator.
Toxicity
LD50 Rat oral 117 mg/kg
1,2-Dibromoethylene's production and use as a research chemical(1) may result in its release to the environment through various waste streams(SRC).
Atmospheric Fate: 1,2-Dibromoethylene does not absorb sunlight at the wavelengths available in the troposphere, so direct photolysis is not expected.|TERRESTRIAL FATE: Based on a classification scheme(1), an estimated Koc value of 29(SRC), determined from a water solubility of 8,910 mg/l(2) and a regression-derived equation(3), indicates that 1,2-dibromoethylene is expected to have very high mobility in soil(SRC). Volatilization of 1,2-dibromoethylene from moist soil surfaces is expected to be an important fate process(SRC) given an estimated Henry's Law constant of 8.5X10-4 atm-cu m/mole(SRC), derived from its vapor pressure, 31 mm Hg(4), and water solubility, 8,910 mg/l(2). The potential for volatilization of 1,2-dibromoethylene from dry soil surfaces may exist(SRC) based upon a vapor pressure of 31 mm Hg(4).|AQUATIC FATE: Based on a classification scheme(1), an estimated Koc value of 29(SRC), determined from a water solubility of 8,910 mg/l(2) and a regression-derived equation(3), indicates that 1,2-dibromoethylene 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 8.5X10-4 atm-cu m/mole(SRC), derived from its vapor pressure, 31 mm Hg(4), and water solubility, 8,910 mg/l(2). Using this Henry's Law constant and an estimation method(3), volatilization half-lives for a model river and model lake are 2.3 and 140 hours, respectively(SRC). According to a classification scheme(5), an estimated BCF of 4(SRC), determined from a water solubility(2) and a regression-derived equation(3), suggests the potential for bioconcentration in aquatic organisms is low(SRC).|ATMOSPHERIC FATE: According to a model of gas/particle partitioning of semivolatile organic compounds in the atmosphere(1), 1,2-dibromoethylene, which has a vapor pressure of 31 mm Hg at 25 °C(2), is expected to exist solely as a vapor in the ambient atmosphere. Vapor-phase 1,2-dibromoethylene is degraded in the atmosphere by reaction with photochemically-produced hydroxyl radicals and ozone molecules(SRC). The half-life for the reaction in air with hydroxyl radicals is estimated to be to be 2.8 days for the cis-isomer and 2.5 days for the trans-isomer of 1,2-dibromoethylene(SRC), calculated from their rate constants of 3.8X10-12 and 4.3X10-12 cu cm/molecule-sec at 25 °C(SRC), respectively, determined using a structure estimation method(3). The half-life for the reaction in air with ozone molecules is estimated to be 670 days for the cis-isomer and 330 days for the trans-isomer of 1,2-dibromoethylene(SRC), calculated from their rate constants of 1.7X10-20 and 3.4X10-20 cu cm/molecule-sec at 25 °C(SRC), respectively, determined using a structure estimation method(3).
... In the troposphere, /1,2-dibromoethylene/ should react with hydroxyl radicals and ozone fairly rapidly. Thus, the rate of atmospheric decomposition will depend upon the concentrations of hydroxyl radicals and ozone.|The rate constants for the vapor-phase reaction of 1,2-dibromoethylene with photochemically-produced hydroxyl radicals have been estimated as 3.8X10-12 cu cm/molecule-sec for the cis-isomer and 4.3X10-12 cu cm/molecule-sec for the trans-isomer at 25 °C(SRC), using a structure estimation method(1). This corresponds to atmospheric half-lives of about 2.8 and 2.5 days at an atmospheric concentration of 5X10+5 hydroxyl radicals per cu cm(1) for the cis- and trans-isomers, respectively. 1,2-Dibromoethylene is not expected to undergo hydrolysis in the environment due to the lack of hydrolyzable functional groups(2) nor to directly photolyze due to the lack of absorption in the environmental UV spectrum (>290 nm).
An estimated BCF of 4 was calculated for 1,2-dibromoethylene(SRC), using a water solubility(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).
44.67 L/kg|The Koc of 1,2-dibromoethylene is estimated as 29(SRC), using a water solubility of 8,910 mg/l(1) and a regression-derived equation(2). According to a classification scheme(3), this estimated Koc value suggests that 1,2-dibromoethylene is expected to have very high mobility in soil.
The Henry's Law constant for 1,2-dibromoethylene is estimated as 8.5X10-4 atm-cu m/mole(SRC), derived from its vapor pressure, 31 mm Hg(1), and water solubility, 8,910 mg/l(2). This Henry's Law constant indicates that 1,2-dibromoethylene is expected to volatilize 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 2.3 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 140 hours(SRC). 1,2-Dibromoethylene's Henry's Law constant indicates that volatilization from moist soil surfaces may occur(SRC). The potential for volatilization of 1,2-dibromoethylene from dry soil surfaces may exist(SRC) based upon a vapor pressure of 31 mm Hg(1).
Since 1,2-dibromoethylene is only used as a research chemical, occupational exposure to 1,2-dibromoethylene may occur through inhalation and dermal contact with this compound at chemical research facilities where 1,2-dibromoethylene is produced or used. (SRC)
Drug Information
Basic treatment: Establish a patent airway. Suction if necessary. Watch for signs of respiratory insufficiency and assist ventilations if needed. Administer oxygen by nonrebreather mask at 10 to 15 L/min. Monitor for pulmonary edema and treat if necessary ... . Monitor for shock and treat if necessary ... . Anticipate seizures and treat if necessary ... . For eye contamination, flush eyes immediately with water. Irrigate each eye continuously with normal saline during transport ... . Do not use emetics. For ingestion, rinse mouth and administer 5 ml/kg up to 200 ml of water for dilution if the patient can swallow, has a strong gag reflex, and does not drool ... . Cover skin burns with dry sterile dressings after decontamination ... . /Poison A and B/|Advanced treatment: Consider orotracheal or nasotracheal intubation for airway control in the patient who is unconscious, has severe pulmonary edema, or is in respiratory arrest. Positive pressure ventilation techniques with a bag valve mask device may be beneficial. Monitor cardiac rhythm and treat arrhythmias as necessary ... . Start an IV with D5W /SRP: "To keep open", minimal flow rate/. Use lactated Ringer's if signs of hypovolemia are present. Watch for signs of fluid overload. Consider drug therapy for pulmonary edema ... . For hypotension with signs of hypovolemia, administer fluid cautiously. Watch for signs of fluid overload ... . Treat seizures with diazepam (Valium) ... . Use proparacaine hydrochloride to assist eye irrigation ... . /Poison A and B/
/CNS DEPRESSANT/ ... IN HIGH CONCN.|1,2-Dibromoethylene is a lachrymator.
1,2-Dibromoethene Use and Manufacturing
... by reaction of tetrabromoethylene with zinc and alc followed by separation of cis- and trans-forms by fractional distillation: Noyes et al, J Am Chem Soc 72: 33 (1950).
RESEARCH CHEM (NO EVIDENCE OF COMMERCIAL USE IN USA)|Chemical syntheses
(1977) 4.5X10+9 G MIN-POSSIBLY AS A BYPRODUCT|(1981) NO EVIDENCE OF COMMERICAL PRODN IN USA
Obtained as a mixture of cis- and trans-isomers.|98%, mixture of cis and trans
Ethene, dibromo-: ACTIVE
Computed Properties
Molecular Weight:185.85
XLogP3:1.9
Exact Mass:185.85028
Monoisotopic Mass:183.85233
Heavy Atom Count:4
Complexity:19.2
Undefined Bond Stereocenter Count:1
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes
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