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Mesityl oxide

Mesityl oxide Structure
CAS No.
141-79-7
Chemical Name:
Mesityl oxide
Synonyms
4-Methylpent-3-en-2-one;mesityl;4-METHYL-3-PENTEN-2-ONE;METHYL ISOBUTENYL KETONE;4-Methyl-3-penten-2-one, 9CI;4-Methyl-3-penten-2-on;Mesityloxid;Mesity oxide;The propyl acetone;isopropyl alcohol-tech
CBNumber:
CB2139085
Molecular Formula:
C6H10O
Molecular Weight:
98.14
MOL File:
141-79-7.mol
MSDS File:
SDS
Modify Date:
2024/6/26 18:14:31

Mesityl oxide Properties

Melting point −53 °C(lit.)
Boiling point 129 °C(lit.)
Density 0.858 g/mL at 25 °C(lit.)
vapor pressure 10.5 hPa (20 °C)
FEMA 3368 | 4-METHYL-3-PENTEN-2-ONE
refractive index n20/D 1.442(lit.)
Flash point 87 °F
storage temp. Store below +30°C.
solubility 30g/l
form Liquid, Free Of Suspended Matter
color Clear
Specific Gravity 0.86
Odor Strong; peppermint; honeylike.
explosive limit 1.4-10.1%(V)
Odor Type vegetable
Water Solubility 28 G/L (20 ºC)
Merck 14,5908
JECFA Number 1131
BRN 1361550
Henry's Law Constant (x 10-6 atm?m3/mol): 4.01 at 20 °C (approximate - calculated from water solubility and vapor pressure)
Exposure limits TLV-TWA 60 mg/m3 (15 ppm) (ACGIH), 10-h TWA 40 mg/m3 (10 ppm) (NIOSH); STEL 100 mg/m3 (25 ppm); IDLH 5000 ppm.
Dielectric constant 15.4(20℃)
Stability Light Sensitive
LogP 1.37 at 20℃
CAS DataBase Reference 141-79-7(CAS DataBase Reference)
NIST Chemistry Reference 3-Penten-2-one, 4-methyl-(141-79-7)
EPA Substance Registry System Mesityl oxide (141-79-7)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS02,GHS06
Signal word  Danger
Hazard statements  H226-H302+H312-H315-H319-H331-H335
Precautionary statements  P210-P280-P301+P312-P303+P361+P353-P304+P340+P311-P305+P351+P338
Hazard Codes  Xn
Risk Statements  10-20/21/22-36/37/38
Safety Statements  25
RIDADR  UN 1229 3/PG 3
OEB A
OEL TWA: 10 ppm (40 mg/m3)
WGK Germany  1
RTECS  SB4200000
Autoignition Temperature 344 °C
TSCA  Yes
HS Code  2914 19 90
HazardClass  3
PackingGroup  III
Toxicity LD50 in mice (mg/kg): 710 ±85 intragastric; LC50 in mice (2 hr), rats (4 hr) (mg/m3): 10000 ±270, 9000 ±600 (Ismerov)
IDLA 1,400 ppm [10% LEL]
NFPA 704
3
3 1

Mesityl oxide price More Price(15)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) W336807 4-Methyl-3-penten-2-one 90% 141-79-7 1SAMPLE ₹4990.33 2022-06-14 Buy
Sigma-Aldrich(India) W336807 4-Methyl-3-penten-2-one 90% 141-79-7 1KG ₹11582.75 2022-06-14 Buy
Sigma-Aldrich(India) W336807 4-Methyl-3-penten-2-one 90% 141-79-7 4KG ₹27809.43 2022-06-14 Buy
Sigma-Aldrich(India) RTC000097 Mesityl Oxide Pharmaceutical Secondary Standard; Certified Reference Material 141-79-7 20ML ₹12351.33 2022-06-14 Buy
Sigma-Aldrich(India) PHR1547 Mesityl Oxide Pharmaceutical Secondary Standard; Certified Reference Material 141-79-7 3X1.2ML ₹9103.83 2022-06-14 Buy
Product number Packaging Price Buy
W336807 1SAMPLE ₹4990.33 Buy
W336807 1KG ₹11582.75 Buy
W336807 4KG ₹27809.43 Buy
RTC000097 20ML ₹12351.33 Buy
PHR1547 3X1.2ML ₹9103.83 Buy

Mesityl oxide Chemical Properties,Uses,Production

Description

The 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.

Chemical Properties

Mesityl oxide is a clear, pale yellow, or colorless liquid with a strong peppermint odor. The odor threshold is 0.05 ppm.

Physical properties

Clear, pale yellow liquid with a strong, peppermint, or honey-like odor. Experimentally determined detection and recognition odor threshold concentrations were 70 μg/m3 (17 ppbv) and 200 μg/m3 (50 ppbv), respectively (Hellman and Small, 1974).

Occurrence

Reported 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

Uses

4-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.

Preparation

4-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.

General Description

Mesityl 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.

Air & Water Reactions

Highly flammable. Slightly soluble in water

Reactivity Profile

Mixing MESITYL OXIDE in equal molar proportions with any of the following substances in a closed container caused the temperature and pressure to increase: 2-aminoethanol, chlorosulfonic acid, ethylene diamine, nitric acid, oleum, or sulfuric acid [NFPA 1991].

Hazard

Flammable, moderate fire risk. Toxic by ingestion, inhalation, and skin absorption. Eye and upper respiratory tract irritant, central nervous system impairment.

Health Hazard

Mesityl oxide is a moderately toxic substance, more toxic than the saturated ketones.Inhalation of its vapors can cause irritationto the eyes, skin, and mucous membranes. Inhumans, the irritation effect on the eyes andnose are reported to be 25 and 50 ppm. Athigh concentrations narcosis can result. Otherthan narcosis, prolonged exposure to highconcentrations can injure the lungs, liver, and kidney. A concentration of 2500 ppm waslethal to rats.
LD50 value, oral (rats): 1120 mg/kg.

Fire Hazard

Behavior in Fire: Vapor is heavier than air and may travel a considerable distance to a source of ignition and flash back.

Safety Profile

Poison by intraperitoneal route. Moderately toxic by ingestion. Mildly toxic by inhalation and skin contact. Human systemic effects by inhalation: conjunctiva irritation. This compound is highly irritating to all tissues on contact; its vapors also are irritating. High concentrations are narcotic. It is readdy absorbed through intact skin. Single exposures tend to indicate that ths ketone has greater acute and narcotic action than isophorone. It can have harmful effects upon the hdneys and liver, and may damage the eyes and lungs to a serious degree. Prolonged exposure can injure liver, kidneys, and lungs. It can cause opaque cornea, keratoconus, and extensive necrosis of cornea. Dangerous fire hazard when exposed to heat, sparks, or flame; can react with oxidzing materials. Reacts violently with 2-amino ethanol, chlorosulfonic acid, ethylene diamine, HNO3, oleum, H2SO4. An insect repellent. To fight fire, use alcohol foam, CO2, dry chemical. When heated to decomposition it emits acrid smoke and irritating fumes. See also KETONES.

Potential Exposure

Mesityl oxide is used as a solvent for cellulose esters and ethers and other resins in lacquers and inks. It is used in paint and varnish removers and as an insect repellent

Shipping

UN1229 Mesitly oxide, Hazard Class: 3; Labels: 3-Flammable liquid.

Purification Methods

Purify it by distillation, preferably in a vacuum or via the semicarbazone (m 165o) which is decomposed to pure ketone. The 2,4-dinitrophenylhydrazone (m 205-206o) crystallises from EtOH. [Johnson J Am Chem Soc 73 5888 1951, Johnson J Am Chem Soc 75 2720 1953, Erskine & Waight J Chem Soc 3425 1960, Beilstein 1 H 736, 1 I 382, 1 II 793, 1 III 2995, 1 IV 3471.]

Incompatibilities

May form explosive mixture with air. May be able to form explosive peroxides. May react violently with nitric acid; aliphatic amines; alkanolamines, 2- aminoethanol, ethylene diamine; chlorosulfonic acid; oleum (fuming sulfuric acid). Not compatible with oxidizers, strong acids; strong bases; reducing agents; halogens. Dissolves some forms of plastics, resins and rubber. Attacks copper.

Waste Disposal

Dissolve or mix the material with a combustible solvent and burn in a chemical incinerator equipped with an afterburner and scrubber. All federal, state, and local environmental regulations must be observed.

Global( 277)Suppliers
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GLR Innovations +91 9891111994 New Delhi, India 4542 58 Inquiry
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Pharma Affiliates 172-5066494 Haryana, India 6761 58 Inquiry
HiMedia Laboratories 91-22-61471919 Maharashtra, India 1843 58 Inquiry
Satyam Petrochemicals 91-2164-264377 Maharashtra, India 2 58 Inquiry
Prasol Chemicals Pvt. Ltd. 91-22-27782555 Maharashtra, India 33 58 Inquiry

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