Grundinformationen
- Standard-SMILES
COC(=O)CCl- InChIKey
QABLOFMHHSOFRJ-UHFFFAOYSA-N- Summenformel
- C3H5ClO2
- Durchschnittliche Molmasse
- 108,52 g/mol
- Monoisotopische Masse
- 107,99780708
Überblick
Methyl chloroacetate appears as a crystalline solid or a solid dissolved in a liquid. Insoluble in water and denser than water. Contact may slightly irritate skin, eyes and mucous membranes. May be slightly toxic by ingestion. Used to make other chemicals.
Namen und Bezeichner
- Bevorzugter Name
- Methyl chloroacetate
- IUPAC
- methyl 2-chloroacetate
- Lokaler Name
- Methylchloracetat
- Englischer Name
- Methyl chloroacetate
- Summenformel
- C3H5ClO2
- Molmasse
- 108.52
Namen und Synonyme
Weitere Namen anzeigen
Datenbank-Bezeichner
- CAS
96-34-4- PubChem CID
- 7295
- DTXSID
DTXSID9041576- UNII
- 450VSB182I
- EC Number
- 202-501-1
- Nikkaji
- J3.968C
Eigenschaften
Berechnete Struktureigenschaften
- XLogP
- 0,7
- Polarare Oberfläche (TPSA)
- 26,3 Ų
- H-Brücken-Donoren
- 0
- H-Brücken-Akzeptoren
- 2
- Frei drehbare Bindungen
- 2
- Schwere Atome
- 6
- Formalladung
- 0
- Komplexität
- 52,8
Experimentelle und physikochemische Eigenschaften
Chemical Classes
Other Classes -> Chloroacetic Acid Derivatives
Corrosives
Density
1.2337 at 68 °F (USCG, 1999) - Denser than water; will sink
1.236 g/cu cm at 20 °C
1.2 g/cm³
Relative density of the vapour/air-mixture at 20 °C (air = 1): 1.02
Color/Form
Liquid
Colorless liquid
Solubility
In water, 4.6X10+4 mg/L at 20 °C
In water, 5.2 g/100 mL at 19.8 °C (5.2X10+4 mg/L)
Miscible with alcohol, ether
Very soluble in acetone, benzene, ethyl ether, ethanol
Miscible with oxygenated solvents
Solubility in water, g/100ml at 19.8 °C: 5.2
Flash Point
125 °F (USCG, 1999)
57 °C
135 °F (57 °C) (open cup)
57 °C o.c.
Boiling Point
266 °F at 760 mmHg (USCG, 1999)
130 °C
BP: 130-132 °C
129.5 °C
Decomposition
Hazardous decomposition products formed under fire conditions: Carbon oxides, hydrogen chloride gas
When heated to decomposition it emits toxic fumes of /hydrogen chloride/.
Physikochemische Eigenschaften
- Schmelzpunkt
- -33 °C · -33 °C
- Siedepunkt
- 130 °C740 · 130 °C740 mm Hg(lit.)
- Dichte
- 1.238 g/mL · 1.238 g/mL at 25 °C(lit.)
- Dampfdichte
- 3.8 · 3.8 (vs air)
- Dampfdruck
- 10 mm · 10 mm Hg ( 25 °C)
- Brechungsindex
- 20 · n20/D 1.422(lit.)
- Flammpunkt
- 125 °F · 125 °F
- storage temp.
- 20 °C · Store at <= 20°C.
- Löslichkeit
- 51.6 g/l · 51.6g/l (slow decomposition)
- Aggregatzustand
- Liquid
- Farbe
- Clear colorless
- PH
- 4.6 · 4.6 (28g/l, H2O, 20℃)
- Explosionsgrenze
- 4.6 · 4.6-18.5%(V)
- Wasserlöslichkeit
- 28 g/L · 28 g/L (20 ºC)
- Merck
- 14 · 14,6042
- BRN
- 506255 · 506255
- Henry's Law Constant
- 4.9 · 4.9×10-1 mol/(m3Pa) at 25℃, Brockbank (2013)
- Dielectric constant
- 12.9 · 12.9(20℃)
- InChI
- 1S/C3H5ClO2/c1-6-3(5)2-4/h2H2,1H3
- InChIKey
- QABLOFMHHSOFRJ-UHFFFAOYSA-N
- SMILES
- ClCC(=O)OC
- LogP
- 0.63 at · 0.63 at 20℃
- CAS Datenbank
- 96 · 96-34-4(CAS DataBase Reference)
- NIST chemische Informationen
- Acetic acid, chloro-, methyl ester(96-34-4)
- EPA chemische Informationen
- 2 · Acetic acid, 2-chloro-, methyl ester (96-34-4)
Sicherheit und Regulatorisches
GHS-Klassifizierung
GHS Classification
Danger
H226: Flammable liquid and vapor [Warning Flammable liquids]
P210, P233, P240, P241, P242, P243, P261, P264, P264+P265, P270, P271, P280, P301+P316, P302+P352, P303+P361+P353, P304+P340, P305+P354+P338, P316, P317, P319, P321, P330, P332+P317, P362+P364, 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 0.6% (1 of 159) of reports.
Danger
H226 (99.4%): Flammable liquid and vapor [Warning Flammable liquids]
Gefahrenhinweise
Regulatory Information
Chemical: Acetic acid, chloro-, methyl ester
Acetic acid, 2-chloro-, methyl ester is listed on the EPA's Chemical Data Reporting (CDR) system. Manufacturers and importers of Acetic acid, 2-chloro-, methyl 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: 10-05-2021 https://echa.europa.eu/registration-dossier/-/registered-dossier/13502
Methyl chloroacetate: HSNO Approval: HSR003022 Approved with controls
The New Jersey Worker and Community Right to Know Act requires public and private employers to provide information about hazardous substances at their workplaces. (N.J.S.A. 34:5A-1 et. seq.)
Fire Hazards
Special Hazards of Combustion Products: Toxic fumes of hydrogen chloride (USCG, 1999)
· HIGHLY FLAMMABLE: Will be easily ignited by heat, sparks or flames.
Flammable. Gives off irritating or toxic fumes (or gases) in a fire. Above 57 °C explosive vapour/air mixtures may be formed.
Health Hazards
Extremely corrosive to the eyes, skin, nose, throat, and upper respiratory tract. Inhalation may be fatal as a result of spasm, inflammation and edema of the larynx and bronchi, chemical pneumonitis, and pulmonary edema. Symptoms of exposure include burning sensation, coughing, wheezing, laryngitis, shortness of breath, headache, nausea, and vomiting. (USCG, 1999)
· TOXIC; may be fatal if inhaled, ingested or absorbed through skin.
Hazards Summary
Corrosive to skin; Severe eye irritant; Respiratory tract irritant; May be absorbed through skin; [ICSC] Toxic by inhalation and ingestion; [eChemPortal: ESIS] Danger of skin sensitization; [MAK] Inhalation may induce upper and lower airway inflammation and edema; [CHRIS] Oral LD50 (mouse) = 240 mg/kg; [RTECS] An irritant; [MSDSonline]
Reactivity Profile
METHYL CHLOROACETATE is a halogenated ester. Esters react with acids to liberate heat along with alcohols and acids. Strong oxidizing acids may cause a vigorous reaction that is sufficiently exothermic to ignite the reaction products. Heat is also generated by the interaction of esters with caustic solutions. Flammable hydrogen is generated by mixing esters with alkali metals and hydrides.
Sicherheit und Schutzausrüstung
Fire Fighting
Excerpt from ERG Guide 131 [Flammable Liquids - Toxic]:
Use water spray, dry powder, alcohol-resistant foam, carbon dioxide. In case of fire: keep drums, etc., cool by spraying with water.
First Aid Measures
Fresh air, rest. 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. Do NOT induce vomiting. Refer for medical attention .
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.
First Aid
Call a physician.
General First Aid:
Exposure Control and Personal Protection
· Wear positive pressure self-contained breathing apparatus (SCBA).
1.0 [ppm]
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. Further information: Use water spray to cool unopened containers.
Cleanup Methods
ACCIDENTAL RELEASE MEASURES; Personal precautions, protective equipment and emergency procedures: Wear respiratory protection. 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: Contain spillage, and then collect with an electrically protected vacuum cleaner or by wet-brushing and place in container for disposal according to local regulations.
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.
Spillage Disposal
Remove all ignition sources. Personal protection: chemical protection suit including self-contained breathing apparatus. Collect leaking and spilled liquid in covered plastic containers as far as possible. Absorb remaining liquid in sand or inert absorbent. Then store and dispose of according to local regulations.
Toxikologische Informationen
Environmental Fate
TERRESTRIAL FATE: Based on a classification scheme(1), an estimated Koc value of 6(SRC), determined from a structure estimation method(2), indicates that methyl chloroacetate is expected to have very high mobility in soil(SRC). Volatilization of methyl chloroacetate from moist soil surfaces is expected to be an important fate process(SRC) given an estimated Henry's Law constant of 2.4X10-5 atm-cu m/mole(SRC), based upon its vapor pressure, 7.63 mm Hg at 25 °C(3), and water solubility, 4600 mg/L(4). Methyl chloroacetate is expected to volatilize from dry soil surfaces(SRC) based upon its vapor pressure(3). Utilizing the Japanese MITI test, 45-95% of the Theoretical BOD was reached in 4 weeks(5) indicating that biodegradation is an important environmental fate process in soil(SRC).
AQUATIC FATE: Based on a classification scheme(1), an estimated Koc value of 6(SRC), determined from a structure estimation method(2), indicates that methyl chloroacetate 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 2.4X10-5 atm-cu m/mole(SRC), derived from its vapor pressure, 7.63 mm Hg(4), and water solubility, 4.6X10+4 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 2 and 16 days, respectively(SRC). According to a classification scheme(6), an estimated BCF of 3(SRC), from an estimated log Kow of 0.63(2) and a regression-derived equation(2), suggests the potential for bioconcentration in aquatic organisms is low(SRC). Utilizing the Japanese MITI test, 45-95% of the Theoretical BOD was reached in 4 weeks(7) indicating that biodegradation is an important environmental fate process in water(SRC). A measured base-catalyzed hydrolysis rate constant of 140 L/mole-sec at 25 °C was reported with corresponding hydrolysis half-lives of 140 to 0.14 hrs at pH values of 6-9(8).
ATMOSPHERIC FATE: According to a model of gas/particle partitioning of semivolatile organic compounds in the atmosphere(1), methyl chloroacetate, which has a vapor pressure of 7.63 mm Hg at 25 °C(2), is expected to exist solely as a vapor in the ambient atmosphere. Vapor-phase methyl chloroacetate 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 65 days(SRC), calculated from its rate constant of 2.5X10-13 cu cm/molecule-sec at 25 °C(3). Methyl chloroacetate does not contain chromophores that absorb at wavelengths >290 nm(4) and, therefore, is not expected to be susceptible to direct photolysis by sunlight(SRC).
Toxicity Summary
IDENTIFICATION AND USE: Methyl chloroacetate (MCA) is a colorless liquid. It is used as a solvent and intermediate. HUMAN STUDIES: In man, delayed occurrence of irritation of the conjunctiva is observed after exposure to the vapor. It was suggested that cross reactivity to MCA may occur in an industrial situation. ANIMAL STUDIES: In guinea-pigs MCA induced sensitization. Cross-sensitization with chloroacetic acid ethyl ester has been observed in this species. MCA is corrosive to rabbit skin and is absorbed through the skin (0.5 mL undiluted substance/rabbit leads to death). The substance is severely irritating to the rabbit eye. In rats MCA produced pronounced eye and respiratory tract irritation at concentrations as low as 250 ppm; some animals exposed to this concentration died within a few days. After repeated inhalation exposure to MCA for 28 days at concentrations of 10, 33 or 100 ppm, adverse effects on the breathing (irregular breathing) and on movement (uncoordinated gait) as well as irritant effects (closing together of the eyelids, sneezing, increased frequency of cleaning) and an increase in relative lung weight occurred in rats at the highest concentration. No increase in the incidence of lung tumors has been established after intraperitoneal administration to strain A mice. MCA was not mutagenic in the Salmonella/microsome test in five strains of Salmonella typhimurium or in Escherichia coli either with or without metabolic activation. No induction of micronuclei has been observed in the micronucleus test in the mouse. ECOTOXICITY STUDIES: Testing the acute toxicity to the Daphnia resulted in a 24 hr EC0 of 3.2 mg/L and a 24 hr EC50 of 5.5 mg/L for inhibition of the swimming capability. The 48 hr and 96 hr LC0 in the zebra fish was 1.13 mg/L. For the rainbow trout, 48 hr LC0 < 2.5 mg/L and 48 hr LC100 of 6 mg/L are reported.
Ecotoxicity Excerpts
/AQUATIC SPECIES/ Testing the acute toxicity to the Daphnia resulted in a 24 hr EC0 of 3.2 mg/L and a 24 hr EC50 of 5.5 mg/L for inhibition of the swimming capability. The 48 hr and 96 hr LC0 in the zebra fish was 1.13 mg/L. For the rainbow trout, 48 hr LC0 < 2.5 mg/L and 48 hr LC100 of 6 mg/L are reported.
Signs and Symptoms
Cough. Shortness of breath. Sore throat.
MAY BE ABSORBED! Redness. Pain. Skin burns.
Redness. Pain. Blurred vision.
Abdominal pain. Nausea. Vomiting. Diarrhoea.
Soil Adsorption/Mobility
Using a structure estimation method based on molecular connectivity indices(1), the Koc of methyl chloroacetate can be estimated to be 6(SRC). According to a classification scheme(2), this estimated Koc value suggests that methyl chloroacetate is expected to have very high mobility in soil(SRC).
TSCA Test Submissions
Methyl chloroacetate (CAS# 96-34-4) was evaluated for acute inhalation toxicity in male and female rats at dose levels of 1.75, 4.26, and 4.44 mg/L for one-hour. Mortality ratios were 0/5 M, 0/5 F; 2/5 M, 3/5 F; and 4/5 M, 4/5 F, respectively. The estimated LC50 value was 3.69 mg/L (831 ppm).
Human Toxicity Excerpts
/HUMAN EXPOSURE STUDIES/ A 23 year old chemical laboratory technician presented with erythema and small blisters on the dorsum of his right hand and forearm. The reaction resulted from a spill of monochloroacetic-acid (MCA). The solution contained 1.5 molar MCA in 94 percent ethanol. He attempted to wash the spill from his arm using water for 10 minutes. After 10 days, the lesions healed, leaving small scars. These scars, after 14 days, became the sites of itchy vesicles. A patch test was performed on day 28, at which time, the patient gave a positive result to the MCA solution at 1 percent in 70 percent methanol. Since it was not considered likely that MCA was the active agent, possible sensitivity to monochloroacetic-acid-ethyl-ester (EMCA) was examined. Strong positive reactions were observed to patch tests with EMCA, whereas the MCA tests were negative. Because plans were underway to use EMCA in a large production process, a guinea-pig maximization test was initiated. Five of the 20 animals tested reacted to EMCA, indicating that this compound is at least a moderate sensitizer. All animals reacted to monochloroacetic-acid-methyl-ester (MMCA). The authors suggest that cross reactivity to MMCA may occur in an industrial situation.
/SIGNS AND SYMPTOMS/ In man, delayed occurrence of irritation of the conjunctiva is observed after exposure to the vapor.
Sicherheitsdaten
- F
- 19
- wgk
- 2
- tsca
- TSCA listed
- ridadr
- UN 2295
- hs_code
- 2915 40 00
- RTECS-Nr.
- AF9500000
- risk_code
- 10-23/25-37/38-41-40-36/37/38-38
- Toxizität
- LD50 orally in Rabbit: 107 mg/kg
- hazard_code
- T,Xi,F
- safety_code
- 26-37/39-45-36-16
- hazard_class
- 6.1
- packing_group
- I
- Speicherklasse
- 3 - Flammable liquids
- Giftige Stoffe Daten
- 96-34-4(Hazardous Substances Data)
- Hazard Classifications
- Acute Tox. 3 InhalationAcute Tox. 3 OralEye Dam. 1Flam. Liq. 3Skin Irrit. 2STOT SE 3
- Selbstentzündungstemperatur
- 869 °F
Chemie und Industrie
Verwendung und Herstellung
Uses
Used as a solvent and chemical intermediate; [Hawley]
Solvent; intermediate
Methyl chloroacetate acts as extraction solvent during the separation of neutral compounds with concentration enhancement using coupling liquid-liquid semimicroextraction with micellar electrokinetic chromatography through on-capillary decomposition. It regenerates the PdCl2-CuCl2/activated carbon catalyst used for synthesis of dimethyl carbonate.
CHEM INT FOR VITAMIN A SYNTHESIS
CHEM INT FOR SODIUM FLUOROACETATE (RODENTICIDE)
CHEM INT FOR RO-7-1051, AN EXPTL ANTIPROTOZOAL AGENT
U.S. Production
2023: <75,000 lb
(1978) PROBABLY GREATER THAN 2.27X10+6 GRAMS
Non-confidential 2016 Chemical Data Reporting (CDR) information on the production and use of chemicals manufactured or imported into the United States. Chemical: Methyl chloroacetate:
Methods of Manufacturing
Methanol and chloroacetic acid (esterification)
Chloroacetate esters are usually made by removing water from a mixture of chloroacetic acid and the corresponding alcohol. Reaction of alcohol with chloroacetyl chloride is an anhydrous process that liberates HCl. Chloroacetic acid will react with olefins in the presence of a catalyst to yield chloroacetate esters. /Chloroacetate esters/
Anwendungen
VerwendenMethyl chloroacetate is used as a solvent and chemical intermediate. It acts as a precursor in the preparation of (carboxymethyl) trimethylammonium chloride esters. Further, it is used in the preparation of octakis-(carbethoxymethoxy)calix[8]arene. It is employed as an extraction solvent during the separation of neutral compounds. In addition to this, it is used in the synthesis of dimethyl carbonate.
Darstellung
synthetischeMethyl chloroacetate is prepared by esterification of chloroacetic acid with methanol. Reaction: Methanol and chloroacetic acid are uniformly mixed in a weight ratio of 0.366:1, heated with stirring, and the esterification reaction is carried out at 105-110 °C. In the reaction process, the ternary azeotrope of methyl chloroacetate, water and methanol is continuously steamed, layered through the ester separator, the separated methanol and water are returned to the reaction pot, and the separated crude ester is made of sodium carbonate. neutralize. The neutralized crude ester is firstly cut out the 130°C fraction by atmospheric distillation, and then subjected to vacuum distillation to collect the 65°C (8kPa) fraction, which is the finished product of methyl chloroacetate. The yield is about 96%.
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