Acute toxicity - Category 2, Oral
Acute toxicity - Category 1, Dermal
Acute toxicity - Category 2, Inhalation
Carcinogenicity, Category 2
H300 Fatal if swallowed
H310 Fatal in contact with skin
H330 Fatal if inhaled
H351 Suspected of causing cancer
P264 Wash ... thoroughly after handling.
P270 Do not eat, drink or smoke when using this product.
P262 Do not get in eyes, on skin, or on clothing.
P280 Wear protective gloves/protective clothing/eye protection/face protection/hearing protection/...
P260 Do not breathe dust/fume/gas/mist/vapours/spray.
P271 Use only outdoors or in a well-ventilated area.
P284 [In case of inadequate ventilation] wear respiratory protection.
P203 Obtain, read and follow all safety instructions before use.
P301+P316 IF SWALLOWED: Get emergency medical help immediately.
P321 Specific treatment (see ... on this label).
P330 Rinse mouth.
P302+P352 IF ON SKIN: Wash with plenty of water/...
P316 Get emergency medical help immediately.
P361+P364 Take off immediately all contaminated clothing and wash it before reuse.
P304+P340 IF INHALED: Remove person to fresh air and keep comfortable for breathing.
P320 Specific treatment is urgent (see ... on this label).
P318 IF exposed or concerned, get medical advice.
P405 Store locked up.
P403+P233 Store in a well-ventilated place. Keep container tightly closed.
P501 Dispose of contents/container to an appropriate treatment and disposal facility in accordance with applicable laws and regulations, and product characteristics at time of disposal.
no data available
Fresh air, rest. Half-upright position. Refer for medical attention.
Remove contaminated clothes. Rinse and then wash skin with water and soap. Refer for medical attention .
First rinse with plenty of water for several minutes (remove contact lenses if easily possible), then refer for medical attention.
Rinse mouth. Induce vomiting (ONLY IN CONSCIOUS PERSONS!). Rest. Refer for medical attention .
This material is very toxic; the probable oral lethal dose is 50-500 mg/kg, or between 1 teaspoonful and 1 ounce for a 150 pound person. It can be a central nervous system depressant in high concentrations. It is extremely irritating to the eyes, nose, and respiratory passages. It can penetrate the skin to cause serious and even fatal poisoning. Poisonous; may be fatal if inhaled, swallowed or absorbed through skin. (EPA, 1998)
Basic treatment: Establish a patent airway. Suction if necessary. Watch for signs of respiratory insufficiency and assist ventilations if necessary. Administer oxygen by nonrebreather mask at 10 to 15 L/min. Provide a low-stimulus environment. 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 . Treat frostbite by rapid rewarming . Ethers and related compounds
Water, foam, mist, fog, spray, dry chemical.
May form phosgene or hydrogen chloride in fires. There is danger of explosion when ethers are heated or exposed to flames or sparks. Ethers tend to form peroxides; when ethers containing peroxides are heated, they can detonate. May be ignited by heat, sparks, or flames. Container may explode in heat of fire. Vapor explosion and poison hazard indoors, outdoors or in sewers. Decomposes in the presence of moisture to form hydrochloric acid. Emits toxic fumes when heated to decomposition. Reacts vigorously with oleum and chlorosulfonic acid. Ethers tend to form peroxides upon standing. Heating peroxide-containing ethers can cause detonation. (EPA, 1998)
Use water spray, foam, powder, carbon dioxide. In case of fire: keep cylinder cool by spraying with water. NO direct contact with water.
Personal protection: chemical protection suit. Ventilation. Remove all ignition sources. Collect leaking and spilled liquid in sealable containers as far as possible. Absorb remaining liquid in sand or inert absorbent. Then store and dispose of according to local regulations.
Personal protection: chemical protection suit. Ventilation. Remove all ignition sources. Collect leaking and spilled liquid in sealable containers as far as possible. Absorb remaining liquid in sand or inert absorbent. Then store and dispose of according to local regulations.
1. remove all ignition sources. 2. ventilate area of spill or leak. 3. for small quantities, absorb on paper towels. evaporate in a safe place (such as a fume hood). allow sufficient time for evaporating vapors to completely clear the hood ductwork. burn the paper in a suitable location away from combustible materials. large quantities can be reclaimed.
NO open flames, NO sparks and NO smoking. Above 55°C use a closed system and ventilation. Handling in a well ventilated place. Wear suitable protective clothing. Avoid contact with skin and eyes. Avoid formation of dust and aerosols. Use non-sparking tools. Prevent fire caused by electrostatic discharge steam.
Fireproof. Separated from food and feedstuffs. See Chemical Dangers. Keep in the dark. Well closed.Store in a cool, dry, well-ventilated location. Store away form heat, oxidizing materials, strong acids, & sunlight.
TLV: 5 ppm as TWA; 10 ppm as STEL; (skin); A4 (not classifiable as a human carcinogen).MAK: 59 mg/m3, 10 ppm; peak limitation category: I(1); skin absorption (H)
no data available
Ensure adequate ventilation. Handle in accordance with good industrial hygiene and safety practice. Set up emergency exits and the risk-elimination area.
Wear face shield or eye protection in combination with breathing protection.
Protective gloves. Protective clothing.
Use ventilation, local exhaust or breathing protection.
no data available
Liquid. Liquid.
Colourless.
PUNGENT
-51.9 °C.
> 172 - < 178 °C. Remarks:The atmospheric pressure at which the boiling point was measured is.
Class II Combustible Liquid: Fl.P. at or above 100°F and below 140°F.
no data available
81 °C. Atm. press.:1 013.25 hPa.
369 °C. Remarks:No data on atmospheric pressure.
no data available
no data available
dynamic viscosity (in mPa s) = 2.41. Temperature:20°C.;dynamic viscosity (in mPa s) = 2.14. Temperature:25°C.
Reaction (NTP, 1992)
log Pow = 1.12. Temperature:20 °C. Remarks:PH.
1.867 hPa. Temperature:25 °C.;0.947 hPa. Temperature:20 °C.
1.219 dimensionless. Temperature:20 °C.;1.213 dimensionless. Temperature:25 °C.
4.93 (EPA, 1998) (Relative to Air)
no data available
NIOSH considers dichloroethyl ether to be a potential occupational carcinogen.
The substance can form explosive peroxides on exposure to air and light. Decomposes on burning. Decomposes on contact with water. This produces toxic fumes including hydrogen chloride. Reacts with strong oxidants. Reacts violently with chlorosulfonic acid and oleum.
no data available
FLAMMABLE LIQUID WHEN EXPOSED TO HEAT, FLAME, OR OXIDANTS.The vapour is heavier than air.2,2'-DICHLORODIETHYL ETHER may form phosgene or hydrogen when heated to high temperature. Oxidizes readily in air to form unstable peroxides that may explode spontaneously [Bretherick, 1979 p.151-154]. Mixing in equal molar portions with the following substances in a closed container caused the temperature and pressure to increase: chlorosulfonic acid and oleum [NFPA 1991].
no data available
It decomposes in presence of moisture to form hydrochloric acid.
When heated to decomp, emits highly toxic fumes of /hydrogen chloride/.
no data available
no data available
no data available
no data available
Cancer Classification: Group B2 Probable Human Carcinogen
No information is available on the developmental or reproductive effects of dichloroethyl ether in humans. In one animal study, no effects were observed on the reproductive tissues of the animals, but no tests on reproductive function were performed.
The substance is irritating to the eyes and respiratory tract. Inhalation of the vapour may cause lung oedema. See Notes. Exposure far above the OEL could cause death. The effects may be delayed. Medical observation is indicated.
Repeated or prolonged contact with skin may cause dermatitis.
A harmful contamination of the air can be reached rather quickly on evaporation of this substance at 20°C.
Bis(2-chloroethyl) ether was added to Ohio River water at pH 7.2 and 22-25 deg C(1). Thirty-five days following the addition of bis(2-chloroethyl) ether to the water, 50% of the carbon dioxide theoretically derivable from bis(2-chloroethyl) ether was recovered. After a second addition of bis(2-chloroethyl) ether, only 9-10 days were required to observe 50% recovery of theoretical carbon dioxide, suggesting acclimation was necessary for optimal biodegradation rates(1). The absence of evidence of biodegradation in another study(2) may be attributed to an insufficiently long acclimation period (18 days)(SRC). Bis(2-chloroethyl) ether, present at 100 mg/l, reached 8.3% of its theoretical BOD in 3 weeks using an activated sludge inoculum(3).
A BCF of 0.4 to 1.3 in carp(1) and a BCF of 11 in bluegills exposed to bis(2-chloroethyl) ether for 14 days(2) was observed. According to a classification scheme(3), these BCF values suggest that the potential for bioconcentration in aquatic organisms is low.
The Koc of bis(2- chloroethyl) ether is estimated as approximately 120(SRC), using a log Kow of 1.29(1) and a regression-derived equation(2,SRC). According to a classification scheme(3), this estimated Koc value suggests that bis(2-chloroethyl) ether is expected to have high mobility in soil(SRC). In a 140 cm long column containing Lincoln fine sand collected in Ada, OK, 86% of the applied bis(2-chloroethyl) ether reached 140 cm, indicating minimal adsorption to this soil(4).
no data available
The material can be disposed of by removal to a licensed chemical destruction plant or by controlled incineration with flue gas scrubbing. Do not contaminate water, foodstuffs, feed or seed by storage or disposal. Do not discharge to sewer systems.
Containers can be triply rinsed (or equivalent) and offered for recycling or reconditioning. Alternatively, the packaging can be punctured to make it unusable for other purposes and then be disposed of in a sanitary landfill. Controlled incineration with flue gas scrubbing is possible for combustible packaging materials.
ADR/RID: UN2810 (For reference only, please check.)
IMDG: UN2810 (For reference only, please check.)
IATA: UN2810 (For reference only, please check.)
ADR/RID: TOXIC LIQUID, ORGANIC, N.O.S. (For reference only, please check.)
IMDG: TOXIC LIQUID, ORGANIC, N.O.S. (For reference only, please check.)
IATA: TOXIC LIQUID, ORGANIC, N.O.S. (For reference only, please check.)
ADR/RID: 6.1 (For reference only, please check.)
IMDG: 6.1 (For reference only, please check.)
IATA: 6.1 (For reference only, please check.)
ADR/RID: I (For reference only, please check.)
IMDG: I (For reference only, please check.)
IATA: I (For reference only, please check.)
ADR/RID: No
IMDG: No
IATA: No
no data available
no data available
The symptoms of lung oedema often do not become manifest until a few hours have passed and they are aggravated by physical effort.Rest and medical observation is therefore essential.Immediate administration of an appropriate inhalation therapy by a doctor or a person authorized by him/her, should be considered.An added stabilizer or inhibitor can influence the toxicological properties of this substance, consult an expert.Check for peroxides prior to distillation; eliminate if found.