Mesityl oxide
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141-79-7CC(=O)C=C(C)CSHOJXDKTYKFBRD-UHFFFAOYSA-NMesityl oxide appears as a colorless, oily liquid with a pungent honey-like odor. Flash point 87 °F. Less dense than water and slightly soluble in water. Vapors heavier than air. Used in paint removers, as a solvent for plastics, and as an insect repellent.
141-79-7DTXSID1029170CHEMBL3185916CHEBI:89993Other Classes -> Aliphatic Ketones, Other
Flammable agents - 3rd degree
... spearmint ...
COMMERCIAL GRADE EXHIBITS AN UNPLEASANT ODOR
Peppermint- or honey-like odor
0.853 at 68 °F (USCG, 1999) - Less dense than water; will float
0.8592 at 15 °C/4 °C
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Warning
H226: Flammable liquid and vapor [Warning Flammable liquids]
P210, P233, P240, P241, P242, P243, P261, P264, P270, P271, P280, P301+P317, P302+P352, P303+P361+P353, P304+P340, P317, P321, P330, P362+P364, P370+P378, P403+P235, and P501 (click each P-code to see the statement)
This chemical does not meet GHS hazard criteria for 0.6% (11 of 1711) of reports.
Danger
H226 (99.4%): Flammable liquid and vapor [Warning Flammable liquids]
Chemical: 3-Penten-2-one, 4-methyl-
Commission Regulation (EC) No 1565/2000 (Repealed by Com. Implementing Reg. (EU) No 872/2012)
3-Penten-2-one, 4-methyl- is listed on the EPA's Chemical Data Reporting (CDR) system. Manufacturers and importers of 3-Penten-2-one, 4-methyl- 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: 19-03-2021 https://echa.europa.eu/registration-dossier/-/registered-dossier/2148
3-Penten-2-one, 4-methyl-: HSNO Approval: HSR001185 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.)
Behavior in Fire: Vapor is heavier than air and may travel a considerable distance to a source of ignition and flash back. (USCG, 1999)
· HIGHLY FLAMMABLE: Will be easily ignited by heat, sparks or flames.
Flammable. Above 25 °C explosive vapour/air mixtures may be formed.
Some mesityl oxide remains unchanged, some reduction and conjugation occurs. Metabolite is believed to be a glucuronide, but has not been demonstrated. /From table/
... Mesityl oxide reacts with certain sulfur-containing compounds in body, probably sulfhydryls and that this forms odorous product which ... /is/ believed to be sulfur substituted ketone.
Mesityl oxide ... reduced in body to apprecialbe extent. ... Shown to increase glucuronic output in rabbits. ... Repeated exposure of animals to non-lethal concentrations, suggests that it is probably not rapidly eliminated, and that with frequent exposures, blood concentration reaches anesthetic level.
It is readily absorbed through the intact skin.
... /Mesityl oxide/ can be absorbed into the body by inhalation of its vapor, through the skin and by ingestion.
Mesityl oxide has many uses as an industrial solvent. It is used as a paint remover and insect repellent. [ACGIH] Used as a solvent for resins, lacquers, enamels, rubber, inks, and oils; [HSDB]
Painting (Solvents) [Category: Paint]
Solvent for nitrocellulose, many gums and resins, particularly vinyl resins. In lacquers, varnishes and enamels. In making methyl isobutyl ketone.
IN LEATHER INDUSTRIES, IN ORE FLOTATION, AS ORGANIC INTERMEDIATE
SYNTHETIC FLAVOR INGREDIENT
SOLVENT FOR RUBBERS, VINYL CHLORIDE-VINYL ACETATE COPOLYMERS, CELLULOSE RESINS, OILS, GUMS, INK, & LACQUERS; COMPONENT OF PAINT AND VARNISH REMOVERS; CHEM INTERMEDIATE FOR METHYL ISOBUTYL KETONE
4-Methyl-4-penten-2-one is the precursor of methyl isobutyl ketone ... and can be produced from acetone in a single- or a two-step process. Pure mesityl oxide is obtained by azeotropic distillation of the crude water-containing product. Subsequent purification by removal of the accompanying impurities, such as mesitylene and phorone ... is effected by distillation.
Wird geladen…
Bulk density = 7.1 lb/gal at 20 °C
0.87 g/cm³
Relative density of the vapour/air-mixture at 20 °C (air = 1): 1.03
0.862-0.868
0.0060 cP at 20 °C
0.75 mm²/s at 20 °C
Flammable liquid.
Dangerous, when exposed to heat or flame; can react with oxidizing materials
Inhalation causes irritation of nose and throat, headache, dizziness, difficult breathing. Contact with liquid or concentrated vapor causes severe eye irritation. Liquid irritates skin. Ingestion causes irritation of mouth and stomach. (USCG, 1999)
· May cause toxic effects if inhaled or absorbed through skin.
Liquid causes first degree burns on short exposure. [CHRIS] Narcosis is induced in acute inhalation studies, and animals develop renal tubular degeneration and hepatic necrosis in subchronic studies. [ACGIH] A lachrymator; [CHEMINFO] A skin irritant and severe eye irritant; [CAMEO]
1229 129
1229 129
Pursuant to section 8(d) of TSCA, EPA promulgated a model Health and Safety Data Reporting Rule. The section 8(d) model rule requires manufacturers, importers, and processors of listed chemical substances and mixtures to submit to EPA copies and lists of unpublished health and safety studies. Mesityl oxide is included on this list.
EPA is withdrawing the final test rule for mesityl oxide (MO; CAS No. 141-79-7). EPA has determined that, since testing of MO has been completed according to the terms of an enforceable consent agreement, testing required under the test rule would be duplicative and therefore, the test rule is no longer needed.
A testing consent order is in effect for mesityl oxide for health effects testing, FR publication date: September 1991.
Mesityl oxide is exempted from the requirement of a tolerance when used as a plant nutrient, cosolvent or solvent in accordance with good agricultural practice as inert (or occasionally active) ingredients in pesticide formulations applied to growing crops only. Limit: Not for use after edible parts of plant begin to form. Do not graze livestock in treated areas within 48 hr after application.
Excerpt from ERG Guide 129 [Flammable Liquids (Water-Miscible / Noxious)]:
Use alcohol-resistant foam, powder, carbon dioxide. In case of fire: keep drums, etc., cool by spraying with water.
Fresh air, rest. Artificial respiration may be needed. Refer immediately 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 immediately for medical attention.
· 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.
Excerpt from NIOSH Pocket Guide for Mesityl oxide:
General First Aid:
(General first aid procedures)
A harmful contamination of the air can be reached rather quickly on evaporation of this substance at 20 °C.
Vapors are heavier than air (vapor-air density at 100 °F, 1.1) and may travel to a source of ignition and flash back.
· Wear positive pressure self-contained breathing apparatus (SCBA).
2.0 [ppm]
Use dry chemical, foam, carbon dioxide, or water spray. Water may be ineffective. Use water spray to keep fire-exposed containers cool.
If material /is/ 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 spread fire. 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.
Aqueous film-forming foam (AFFF), alcohol-resistant foam, powder, carbon dioxide.
Fireproof. Separated from strong oxidants. Cool. Keep in the dark.
Protect containers against physical damage. Store well-ventilated cool place, isolating from oxidizing materials. Outdoor or isolated place from inhabitants is preferable. In case of outdoor storage, use standard combustible liquid storage room or cabinet.
Eliminate all ignition sources. Stop or control the leak, if it can be done without undue risk. Use appropriate foam to blanket release and suppress vapors. Approach release from upwind. Absorb in noncombustible material for proper disposal.
Absorb on paper. Evaporate on a glass or iron dish in hood. Burn the paper.
Ventilation. Collect leaking liquid in sealable containers. Absorb remaining liquid in sand or inert absorbent and remove to safe place. Do NOT wash away into sewer. (Extra personal protection: self-contained breathing apparatus).
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 quality; potential migration in soil or water; effects on animal, aquatic, and plant life; and conformance with environmental and public health regulations.
TERRESTRIAL FATE: Based on a classification scheme(1), an estimated Koc value of 15(SRC), determined from a water solubility of 28,900 mg/L(2) and a regression-derived equation(3), indicates that mesityl oxide is expected to have very high mobility in soil(SRC). Volatilization of mesityl oxide from moist soil surfaces is expected to be an important fate process(SRC) given an estimated Henry's Law constant of 3.67X10-5 atm-cu m/mole(SRC), derived from its vapor pressure, 8.21 mm Hg(4), and water solubility(2). Mesityl oxide is expected to volatilize from dry soil surfaces(SRC) based upon its vapor pressure(4). Theoretical %BOD values of 74(5) and 30(6) from studies done with sewage inoculum suggest that biodegradation may be an important environmental fate process in soil(SRC).
AQUATIC FATE: Based on a classification scheme(1), an estimated Koc value of 15(SRC), determined from a water solubility of 28,900 mg/L(2) and a regression-derived equation(3), indicates that mesityl oxide 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 3.67X10-5 atm-cu m/mole(SRC), derived from its vapor pressure, 8.21 mm Hg(4), and its water solubility(2). Using this Henry's Law constant and an estimation method(3), volatilization half-lives for a model river and model lake are 17 hours and 11 days, respectively(SRC). According to a classification scheme(5), an estimated BCF of 1.9(SRC), using a water solubility of 28,900 mg/L(2) and a regression-derived equation(6), suggests the potential for bioconcentration in aquatic organisms is low(SRC). Theoretical %BOD values of 74(7) and 30(8) from studies done with sewage inoculum suggest that biodegradation may be an important environmental fate process in water(SRC).
ATMOSPHERIC FATE: According to a model of gas/particle partitioning of semivolatile organic compounds in the atmosphere(1), mesityl oxide, which has a vapor pressure of 8.21 mm Hg at 25 °C(2), is expected to exist solely as a vapor in the ambient atmosphere. Vapor-phase mesityl oxide 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 4.9 hours(SRC), calculated from its rate constant of 7.86X10-11 cu cm/molecule-sec at 25 °C(SRC) that was derived using a structure estimation method(3). The rate constant for the vapor-phase reaction of mesityl oxide with ozone has been estimated as 2X10-16 cu cm/molecule-sec at 25 °C(SRC) that was derived using a structure estimation method(3). This corresponds to an atmospheric half-life of about 1.4 hours at an atmospheric concentration of 7X10+11 ozone molecules per cu cm(4). The rate constant for the vapor-phase reaction of mesityl oxide with nitrate has been estimated as 2.04X10-13 cu cm/molecule-sec at 25 °C(5). This corresponds to an atmospheric half-life of about 3.9 hours at an atmospheric concentration of 2.4X10+8 nitrate molecules per cu cm(6). Vapor-phase mesityl oxide undergoes direct photolysis with an experimental half-life and rate constant of 76.8 hrs and 8.75X10-3/hr, respectively(7).
The substance can be absorbed into the body by inhalation of its vapour and by ingestion.
inhalation, ingestion, skin and/or eye contact
Cough. Sore throat. Shortness of breath. Headache. Dizziness. Drowsiness. Unconsciousness. Respiratory and cardiac arrest.
Dry skin. Redness. Pain.
Redness. Pain.
Abdominal cramps. Further see Inhalation.
irritation eyes, skin, mucous membrane; narcosis, coma; In Animals: liver, kidney damage; central nervous system effects
Exhaust from an automobile using various hydrocarbon fuels under simulated city conditions yielded concentrations of <0.1-1.5 ppm of mesityl oxide(1). Qualitatively detected in Lockport, IL oil refinery final effluent(2) and in advanced waste water treatment concentrates from Orange County and Lake Tahoe, CA(3-5). In a comprehensive survey of 46 industrial and publicly owned treatment works, mesityl oxide was qualitatively identified in effluents from various organic chemical manufacturing sites(6).
The Koc of mesityl oxide is estimated as 15(SRC), using a water solubility of 28,900 mg/L(1) and a regression-derived equation(2). According to a classification scheme(3), this estimated Koc value suggests that mesityl oxide is expected to have very high mobility in soil.
Pursuant to section 8(d) of TSCA, EPA promulgated a model Health and Safety Data Reporting Rule. The section 8(d) model rule requires manufacturers, importers, and processors of listed chemical substances and mixtures to submit to EPA copies and lists of unpublished health and safety studies. Mesityl oxide is included on this list.
EPA is withdrawing the final test rule for mesityl oxide (MO; CAS No. 141-79-7). EPA has determined that, since testing of MO has been completed according to the terms of an enforceable consent agreement, testing required under the test rule would be duplicative and therefore, the test rule is no longer needed.
A testing consent order is in effect for mesityl oxide for health effects testing, FR publication date: September 1991.
Mesityl oxide is exempted from the requirement of a tolerance when used as a plant nutrient, cosolvent or solvent in accordance with good agricultural practice as inert (or occasionally active) ingredients in pesticide formulations applied to growing crops only. Limit: Not for use after edible parts of plant begin to form. Do not graze livestock in treated areas within 48 hr after application.
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. Mesityl oxide is produced, as an intermediate or a final product, by process units covered under this subpart.
2023: <75,000 lb
This chemical is listed as a High Production Volume (HPV) (65FR81686). Chemicals listed as HPV were produced in or imported into the U.S. in >1 million pounds in 1990 and/or 1994. The HPV list is based on the 1990 Inventory Update Rule. (IUR) (40 CFR part 710 subpart B; 51FR21438).
(1973) 1.23X10+10 GRAMS (ACETONE USED IN MFR)
(1975) 2.07X10+10 GRAMS
Production volumes for non-confidential chemicals reported under the Inventory Update Rule. [Table#2980]
Dehydration of acetone or diacetone alcohol.
Made by distilling diacetone alcohol with a small amount of iodine; ... condensation of acetone to mesityl oxide using sulfonated polystyrene-divinylbenzene resin as ion exchange catalyst.
Grade: Technical
Grades of purity: 97+%
Fragrance Ingredients
Flavouring Agent -> FLAVOURING_AGENT -> JECFA Functional Classes
Flavoring Agents -> JECFA Flavorings Index
Flavouring Agent -> FLAVOURING_AGENT -> JECFA Functional Classes
Flavouring Agent -> FLAVOURING_AGENT -> JECFA Functional Classes
Flavouring Agent -> FLAVOURING_AGENT -> JECFA Functional Classes
Not Known or Reasonably Ascertainable
3-Penten-2-one, 4-methyl-: ACTIVE
FLAVORS USEFUL IN PEPPERMINT AND SPEARMINT.
BeschreibungThe commercial grade of 4-methyl-3-penten-2-one exhibits an unpleasant grassy-green or pungent, acrylic odor. The pure material has a pleasant, honey-like odor. This substance may be prepared by reacting acetone or diacetone alcohol with iodine or other dehydrating agent; by condensation of acetone over sulfonated polystyrene-divinylbenzene resin used as an ion exchange catalyst.
OccurrenceReported found in orange juice, baked potato, bell pepper, sauerkraut, tomato, crisp bread, parmesan cheese, milk, chicken fat, hop oil, rum, coffee, tea, peanut, passion fruit, mushroom, tamarind, prickly pear, buckwheat, basil, elder flower, rosemary, shrimp, nectarine, clam and maté
Verwenden4-Methyl-4-penten-2-one is used to a small extent as an intermediate in synthesis. Most of it is converted to 4-methyl-2-pentanone by selective hydrogenation. Although 4-methyl-2- pentanone has excellent solvent properties for nitrocellulose, cellulose esters and ethers, copolymers of vinyl chloride – vinyl acetate and other synthetic resins, as well as natural and synthetic rubber, its use as a solvent is limited as a result of its toxicity and chemical instability. The fraction of 4-methyl-4-penten-2-one permitted in solvent systems has been set at 5 vol% (Rule 66 of the Los Angeles, California, Air Pollution Control District). Some of the numerous possible reactions that mesityl oxide may undergo have been used for the synthesis of products such as Budralazine, an antihypertensive agent.
synthetische4-Methyl-4-penten-2-one is the precursor of methyl isobutyl ketone (see Section 2.2) and can be produced from acetone in a single- or a two-step process . Pure mesityl oxide is obtained by azeotropic distillation of the crude watercontaining product. Subsequent purification by removal of the accompanying impurities, such as mesitylene and phorone [504-20-1], is effected by distillation.