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Methylacetoacetat
MAA · METHYL 3-OXOBUTANOATE · ACM · Methylacetoacetic acid · ACETOACETIC ACID METHYL ESTER · METHYL ACETOACETAT · METHYL 3-OXOBUTYRATE · Molybdic acid monohydrate

Identifikatoren & physikalische Daten
| CAS No. | 105-45-3 |
|---|---|
| Summenformel | C5H8O3 |
| Durchschnittliche Molmasse | 116,11 g/mol |
| Monoisotopische Masse | 116,04734412 g/mol |
| SMILES | COC(=O)CC(C)=O |
| InChIKey | WRQNANDWMGAFTP-UHFFFAOYSA-N |
| PubChem CID | 7757 |
| ChEMBL | CHEMBL3186053 |
| ChEBI | CHEBI:166454 |
| EC No. | 203-299-8 |
| DTXSID | DTXSID9026716 |
| Lokaler Name | Methylacetoacetat |
Chemische & physikalische Eigenschaften
| XLogP | 0 |
|---|---|
| Polarare Oberfläche (TPSA) | 43,4 |
| H-Brücken-Donoren | 0 |
| H-Brücken-Akzeptoren | 3 |
| Frei drehbare Bindungen | 3 |
| Schwere Atome | 8 |
| Formalladung | 0 |
| Komplexität | 106 |
| Solvents | Solvents -> Esters (<C12) |
| SpringerMaterials Properties | Boiling point |
| Duftstoffe | Fragrance Ingredient (Methyl acetoacetate) -> IFRA transparency List |
| LogP (Verteilungskoeffizient) | log Kow = -0.69 /Estimated/-0.26 |
| Geruch | Agreeable odor |
| Dichte | 1.076 (USCG, 1999) - Denser than waterwill sink1.0762 g/cu cm at 20 °CBulk density: 9 lb/gal at 20 °CRelative density (water = 1): 1.081.076 g/mL at 25 °C (lit.) |
| Aromastoffe | EU Flavoring substances |
| Viscosity | 1.704 cPa at 20 °C |
| Color/Form | Colorless liquid |
| Löslichkeit | Soluble in 2 parts watermiscible with alcohol and etherSOLUBILITY IN WATER: 38 G/100 ML500.0 mg/mLSolubility in water, g/100ml: 50460 g/L (20°C)460 g/L (20 ºC) |
| Flammpunkt | 158 °F (USCG, 1999)170 °F (77 °C) (open cup)77 °C c.c. |
| Siedepunkt | 336 to 338 °F at 760 mmHg (USCG, 1999)171.7 °C169.00 °C. @ 760.00 mm Hg169-170 °C/70 mmHg (lit.) |
| Schmelzpunkt | -80 °C (lit.) |
| Dampfdichte | 4 (vs air) |
| Dampfdruck | 1 hPa (20 °C) |
| Brechungsindex | n20/D 1.419(lit.) |
| Lagerbedingungen | 2-8°C |
| pKa (Säurekonstante) | 10.67±0.46(Predicted) |
| Aggregatzustand | Liquid |
| Farbe | APHA: ≤20 |
| Geruch | at 100.00 %. fresh fruity citrus green |
| pH | 3.8 (863g/l, H2O, 20℃) |
| Explosionsgrenze | 1.3-14.2%(V) |
| Geruchsart | fruity |
| Merck | 14,6009 |
| BRN | 506727 |
| Henry-Konstante | 6.4×100 mol/(m3Pa) at 25℃, \vS (2002) |
| Kosmetik-Inhaltsstoffe Funktionen | PERFUMING |
| InChI | 1S/C5H8O3/c1-4(6)3-5(7)8-2/h3H2,1-2H3 |
| InChIKey | WRQNANDWMGAFTP-UHFFFAOYSA-N |
| SMILES | COC(=O)CC(C)=O |
| LogP (Verteilungskoeffizient) | 0.185 (est) |
| CAS Datenbank | 105-45-3(CAS DataBase Reference) |
| NIST chemische Informationen | Butanoic acid, 3-oxo-, methyl ester(105-45-3) |
| EPA chemische Informationen | Methyl acetoacetate (105-45-3) |
Sicherheit & Vorschriften
| GHS-Einstufung | WarningH319: Causes serious eye irritation [Warning Serious eye damage/eye irritation]P264+P265, P280, P305+P351+P338, and P337+P317 (click each P-code to see the statement)This chemical does not meet GHS hazard criteria for 0.6% (12 of 1934) of reports.H319 (95.7%): Causes serious eye irritation [Warning Serious eye damage/eye irritation] |
|---|---|
| Regulatorische Informationen | Chemical: Butanoic acid, 3-oxo-, methyl esterCommission Regulation (EC) No 1565/2000 (Repealed by Com. Implementing Reg. (EU) No 872/2012)Butanoic acid, 3-oxo-, methyl ester is listed on the EPA's Chemical Data Reporting (CDR) system. Manufacturers and importers of Butanoic acid, 3-oxo-, 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: 09-02-2022 https://echa.europa.eu/registration-dossier/-/registered-dossier/13864Methyl acetoacetate: Does not have an individual approval but may be used under an appropriate group standard |
| DOT-Kennzeichnung | Combustible Liquid |
| Brandgefahren | Excerpt from ERG Guide 128 [Flammable Liquids (Water-Immiscible)]:Combustible. Above 77 °C explosive vapour/air mixtures may be formed. |
| Brandpotenzial | FIRE HAZARD: Moderate, when exposed to heat or flame. |
| Gesundheitsgefahren | May be harmful by inhalation, ingestion, or skin absorption. Causes eye irritation. May cause skin irritation. (USCG, 1999) |
| Gefahrenübersicht | A skin, eye, and respiratory tract irritantMay cause CNS depression[ICSC] An eye irritant[CAMEO] A severe eye irritant based on animal studies[CHEMINFO] An irritant[MSDSonline] |
| Reaktive Gruppe | Esters, Sulfate Esters, Phosphate Esters, Thiophosphate Esters, and Borate Esters |
| EG-Einstufung | Symbol: XiR: 36S: (2)-26 |
| Special Reports | OPDYKE DL JMONOGRAPHS ON FRAGRANCE RAW MATERIALS. METHYL ACETOACETATEFOOD COSMET TOXICOL 16 (SUPPL 1): 815 (1978). A REVIEW WITH 12 REFERENCES ON METHYL ACETOACETATE INCL TOXICITY, IRRITATION, SENSITIZATION & NUTRITION.EPA/Office of Pollution Prevention and ToxicsHigh Production Volume (HPV) Challenge Program's Robust Summaries and Test Plans. Available from: http://www.epa.gov/chemrtk/viewsrch.htm on Methyl acetoacetate as of November 2, 2004.The U.S. high production volume (HPV) chemicals are those which are manufactured in or imported into the United States in amounts equal to or greater than one million pounds per year. Robust Summaries include health effects, ecotoxicity data, and environmental fate information for selected chemicals. EPA/Office of Pollution Prevention and Toxics |
| Reactivity Profile | METHYL ACETOACETATE is an 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 |
| Luftstandards | 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. Methyl acetoacetate is produced, as an intermediate or a final product, by process units covered under this subpart. |
| Chemical Dangers | Decomposes on burning. This produces irritating fumes. Reacts with oxidants. |
| Brandbekämpfung | Excerpt from ERG Guide 128 [Flammable Liquids (Water-Immiscible)]:Use alcohol-resistant foam, powder, carbon dioxide. |
| Erste-Hilfe-Maßnahmen | Fresh air, rest. Refer for medical attention.Remove contaminated clothes. Rinse skin with plenty of water or shower.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. Give one or two glasses of water to drink. Refer for medical attention . |
| Erste Hilfe | INHALATION: Call for medical aid. Remove to fresh air. If not breathing, give aritificial respiration. If breathing is difficult, give oxygen. |
| Sichere Lagerung | Separated from oxidants. |
| Brandbekämpfungsverfahren | ... /Use/ foam, carbon dioxide, dry chemical.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 be ineffective. 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. |
| Freisetung ohne Brand | Excerpt from ERG Guide 128 [Flammable Liquids (Water-Immiscible)]: |
| Entsorgungsverfahren | 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 qualitypotential migration in soil or watereffects on animal, aquatic, and plant lifeand conformance with environmental and public health regulations. |
| Verschüttetes entsorgen | Personal protection: filter respirator for organic gases and vapours adapted to the airborne concentration of the substance. Ventilation. Collect leaking and spilled liquid in sealable containers as far as possible. Wash away remainder with plenty of water. |
| Preventive Measures | If material not on fire and not involved in fire: Keep sparks, flames, and other sources of ignition away. Keep material out of water sources and sewers. Build dikes to contain flow as necessary. Use water spray to knock-down vapors.Personnel protection: Avoid breathing vapors. Keep upwind. ... Do not handle broken packages unless wearing appropriate personal protective equipment. Wash away any material which may have contacted the body with copious amounts of water or soap and water.SRP: The scientific literature for the use of contact lenses in industry is conflicting. The benefit or detrimental effects of wearing contact lenses depend not only upon the substance, but also on factors including the form of the substance, characteristics and duration of the exposure, the uses of other eye protection equipment, and the hygiene of the lenses. However, there may be individual substances whose irritating or corrosive properties are such that the wearing of contact lenses would be harmful to the eye. In those specific cases, contact lenses should not be worn. In any event, the usual eye protection equipment should be worn even when contact lenses are in place. |
| Isolation and Evacuation | Excerpt from ERG Guide 128 [Flammable Liquids (Water-Immiscible)]: |
| Eye Prevention | Wear safety goggles. |
| Fire Prevention | NO open flames. Above 77 °C use a closed system and ventilation. |
| Ökotoxizitätswerte | EC50 Daphnia magna (Water fleaAcute immobilization test and reproduction) >236.9 mg/L/48 hrstaticexposure temperature ranged from 20-21 °C, pH ranged from 7.9 to 8.3, and dissolved oxygen ranged from 8.7 to 8.9 mg/LLC50 Pimephales promelas (Fathead minnow) >111.4 mg/L/96 hrtemperature ranged from 19-20 °C, pH ranged from 7.7 to 8.4 and dissolved oxygen ranged from 7.8 to 9.1 mg/L.EC50 Selenastrum capriconutum (cell growth rate) >978.0 mg/L/24 hr, 48 hr, 72 hr /Conditions of bioassay not specified in source examined/ |
| Umweltverhalten | TERRESTRIAL FATE: Based on a classification scheme(1), an estimated Koc value of 1.0(SRC), determined from a structure estimation method(2), indicates that methyl acetoacetate is expected to have very high mobility in soil(SRC). Volatilization of methyl acetoacetate from moist soil surfaces is expected to be slow(SRC) given an estimated Henry's Law constant of 2.7X10-7 atm-cu m/mole(SRC), derived from its vapor pressure of 0.892 mm Hg(3), and water solubility, 5X10+5 mg/L(4). A base-catalyzed second-order hydrolysis rate constant of 0.57 L/mole-sec(SRC) was estimated using a structure estimation method(5)this corresponds to half-lives of 140 and 14 days at pH values of 7 and 8, respectively(5). Methyl acetoacetate would be expected to hydrolyze in moist soil under basic conditions(SRC). Methyl acetoacetate is not expected to volatilize from dry soil surfaces(SRC) based upon a vapor pressure of 0.892 mm Hg(3). One screening test observed 78% biodegradation of methyl acetoacetate in 14 days(6)although this study was not specific to soil, it suggests that biodegradation in soil may be rapid(SRC).AQUATIC FATE: Based on a classification scheme(1), an estimated Koc value of 1.0(SRC), determined from a structure estimation method(2), indicates that methyl acetoacetate is not expected to adsorb to suspended solids and sediment(SRC). Volatilization from water surfaces is expected to be slow(3) based upon an estimated Henry's Law constant of 2.7X10-7 atm-cu m/mole(SRC), derived from its vapor pressure of 0.892 mm Hg(4), and water solubility, 5X10+5 mg/L(5). A base-catalyzed second-order hydrolysis rate constant of 0.57 L/mole-sec(SRC) was estimated using a structure estimation method(6)this corresponds to half-lives of 140 and 14 days at pH values of 7 and 8, respectively(6). According to a classification scheme(7), an estimated BCF of 3.1(SRC), from an estimated log Kow of -0.69(8) and a regression-derived equation(9), 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), methyl acetoacetate, which has a vapor pressure of 0.892 mm Hg at 25 °C(2), is expected to exist solely as a vapor in the ambient atmosphere. Vapor-phase methyl acetoacetate 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 5 days(SRC), calculated from its rate constant of 3.25X10-13 cu cm/molecule-sec at 25 °C(3). Methyl acetoacetate does not absorb light with wavelengths >290 nm(4) and is not expected to be susceptible to direct photolysis by sunlight(SRC). |
| Unerwünschte Wirkungen | Neurotoxin - Acute solvent syndrome |
| Expositionspfade | The substance can be absorbed into the body by inhalation of its vapour. |
| Signs and Symptoms | Cough. Dizziness. Drowsiness. Headache. Sore throat.Redness. Pain. |
| Soil Adsorption/Mobility | Using a structure estimation method based on molecular connectivity indices(1), the Koc for methyl acetoacetate can be estimated to be 1.0(SRC). According to a classification scheme(2), this estimated Koc value suggests that methyl acetoacetate is expected to have very high mobility in soil. |
| Natural Pollution Sources | Methyl acetoacetate was found in the condensed smoke of fires of ponderosa pine sapwood, needles, bark, litter, duff, and humus(1). |
| Artificial Pollution Sources | Methyl acetoacetate's production and use as a solvent for cellulose ethers and esters and in organic synthesis(1) may result in its release to the environment through various waste streams(SRC). |
| Environmental Biodegradation | AEROBIC: Methyl acetoacetate, present at 100 mg/L, reached 78% of its theoretical BOD in 2 weeks using an activated sludge inoculum at 30 mg/L and the Japanese MITI test(1). Methyl acetoacetate was degraded more than 90% in 2 days at 22 °C using activated sludge inoculum in a Zahn-Wellens screening test(2). |
| Environmental Bioconcentration | An estimated BCF of 3.1 was calculated for methyl acetatoactate(SRC), using an estimated log Kow of -0.69(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). |
| Volatilization from Water/Soil | The Henry's Law constant for methyl acetoacetate is estimated as 2.7X10-7 atm-cu m/mole(SRC) derived from its vapor pressure, 0.894 mm Hg(1), and water solubility, 5X10+5 mg/L(2). This Henry's Law constant indicates that methyl acetoacetate is expected to volatilize slowly from water surfaces(3). Methyl acetoacetate's estimated Henry's Law constant indicates that volatilization from moist soil surfaces may occur(SRC). Methyl acetoacetate is not expected to volatilize from dry soil surfaces(SRC) based upon its vapor pressure(1). |
| Non-Human Toxicity Excerpts | /LABORATORY ANIMALS: Acute Exposure/ An 8-hr exposure to saturated vapor was not lethal to rats./LABORATORY ANIMALS: Acute Exposure/ ...Slightly to moderately irritating to the eyes and skin /of rats/./LABORATORY ANIMALS: Acute Exposure/ /Rats/ dosed /orally/ at 1.0 or 2.0 g/kg were observed to be sluggish and unkempt following intubation. Within 48 hr animals returned to normal behavior and appearance. Animals dosed at 2.5 to 4.0 g/kg exhibited lethargy, nasal hemorrhage and dirty, unkempt coats. At 8.0 g/kg all animals became comatose immediately following intubation and succumbed within 15 minutes of exposure. No postmortem or histopathology examinations were performed on any animals./LABORATORY ANIMALS: Subchronic or Prechronic Exposure/ /Male and female/ Sprague-Dawley (Crl:CDB BR) /rats were dosed/ daily /by/ oral gavage /for a/ 4-wk exposure with 2-wk recovery for control and high dose subgroups. Dose levels: 0, 100, 300, and 1000 mg/kg/daycontrols received vehicle (water). There were no premature deaths during the study. No clinical signs observed were considered to be as a result of treatment with the test substance. There were no notable intergroup body weight, food or water consumption differences in either sex. There were no effects noted in hematology, clinical chemistries or urinalyses considered to be toxicologically significant in either sex. There were no intergroup differences in either organ weights, necropsy or histological findings that were considered to be treatment related in either sex. On completion of 4 weeks of dosing all main study animals were sacrificed and necropsied and given a detailed post mortem examination with organs being weighed ( i.e. adrenals, brain, kidney, liver, ovaries and testis with epididymis) and tissues preserved in fixative (i.e. all abnormal tissue, adrenals, brain, ears, eyes, heart, kidney, liver, lung, marrow smear, optic nerve, ovaries, pituitary, spleen stomach, testis with epididymis, thyroid with parathyroid and urinary bladder). Histological examination was carried out on all control and high dose animals. After the 2 week recovery period all recovery study animals were sacrificed and processed in an identical manner.For more Non-Human Toxicity Excerpts (Complete) data for METHYL ACETOACETATE (8 total), please visit the HSDB record page. |
| Wassergefährdungsklasse (WGK) | 1 |
| TSCA-Inventar-Status | TSCA listed |
| UN-Transportnummer | NA1993 |
| Zollcode | 29183000 |
| RTECS-Nr. | AK5775000 |
| R-Sätze (R) | 36 |
| Toxizität | LD50 orally in rats: 3.0 g/kg (Smyth, Carpenter) |
| Gefahrensymbole | Xi |
| Sicherheitshinweise (S) | 26 |
| Gefahrenklasse | CBLEye Dam. 1 |
| Lagerklasse | 10 - Combustible liquids |
| Gefahrstoffdaten | 105-45-3(Hazardous Substances Data) |
| Selbstentzündungstemperatur | 536 °F |
Anwendungen & Verwendung
Verwenden
Methyl acetoacetate (MAA) is a starting material for the syntheses of alpha-substituted aceto- acetic esters and cyclic compounds, e.g. pyrazole, pyrimidine and coumarin derivatives.