ChemicalBook > CAS DataBase List > Methyl methacrylate

Methyl methacrylate

Product Name
Methyl methacrylate
CAS No.
80-62-6
Chemical Name
Methyl methacrylate
Synonyms
MMA;Mme;Methylmetacrylate;Methyl methylacrylate;Methyl 2-methylacrylate;METHYL 2-METHYL-2-PROPENOATE;METHYL METACRYLAT;Methyl-methacrylat;2-METHYLACRYLIC ACID METHYL ESTER;2-Methyl-2-propenoic acid methyl ester
CBNumber
CB8854425
Molecular Formula
C5H8O2
Formula Weight
100.12
MOL File
80-62-6.mol
More
Less

Methyl methacrylate Property

Melting point:
-48 °C (lit.)
Boiling point:
100 °C (lit.)
Density 
0.936 g/mL at 25 °C (lit.)
vapor density 
3.5 (vs air)
vapor pressure 
29 mm Hg ( 20 °C)
refractive index 
n20/D 1.414(lit.)
FEMA 
4002 | METHYL 2-METHYL-2-PROPENOATE
Flash point:
50 °F
storage temp. 
2-8°C
solubility 
15g/l
form 
Crystalline Powder or Crystals
color 
White to pale yellow
Odor
at 0.10 % in dipropylene glycol. acrylic aromatic fruity
Odor Type
acrylate
Odor Threshold
0.21ppm
explosive limit
2.1-12.5%(V)
Water Solubility 
15.9 g/L (20 ºC)
Merck 
14,5941
JECFA Number
1834
BRN 
605459
Henry's Law Constant
2.46 x 10-4 atm?m3/mol at 20 °C (approximate - calculated from water solubility and vapor pressure)
Exposure limits
NIOSH REL: TWA 100 ppm (410 mg/m3), IDLH 1,000 ppm; OSHA PEL: TWA 100 ppm; ACGIH TLV: TWA 100 ppm with intended TWA and STEL values of 50 and 100 ppm, respectively.
Dielectric constant
2.9（20℃）
Stability:
Volatile
InChIKey
VVQNEPGJFQJSBK-UHFFFAOYSA-N
LogP
1.38 at 20℃
CAS DataBase Reference
80-62-6(CAS DataBase Reference)
NIST Chemistry Reference
2-Propenoic acid, 2-methyl-, methyl ester(80-62-6)
IARC
3 (Vol. Sup 7, 60) 1994
EPA Substance Registry System
Methyl methacrylate (80-62-6)
More
Less

Safety

Hazard Codes 
F,Xi,T
Risk Statements 
11-37/38-43-39/23/24/25-23/24/25
Safety Statements 
24-37-46-45-36/37-16-7
RIDADR 
UN 1247 3/PG 2
OEB
A
OEL
TWA: 100 ppm (410 mg/m3)
WGK Germany 
1
RTECS 
OZ5075000
Autoignition Temperature
815 °F
TSCA 
Yes
HazardClass 
3
PackingGroup 
II
HS Code 
29161410
Hazardous Substances Data
80-62-6(Hazardous Substances Data)
Toxicity
The acute toxicity of methyl methacrylate is low. Irritation of the skin, eye, and nasal cavity has been observed in rodents and rabbits exposed to relatively high concentrations of methyl methacrylate. The chemical is a mild skin sensitizer in animals. The effect observed most frequently at lowest concentration after repeated inhalation exposure to methyl methacrylate is irritation of the nasal cavity. Effects on the kidney and liver at higher concentrations have also been reported.
IDLA
1,000 ppm
More
Less

Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Danger
Hazard statements

H225Highly Flammable liquid and vapour

H315Causes skin irritation

H317May cause an allergic skin reaction

H335May cause respiratory irritation

Precautionary statements

P210Keep away from heat/sparks/open flames/hot surfaces. — No smoking.

P233Keep container tightly closed.

P240Ground/bond container and receiving equipment.

P241Use explosion-proof electrical/ventilating/lighting/…/equipment.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P303+P361+P353IF ON SKIN (or hair): Remove/Take off Immediately all contaminated clothing. Rinse SKIN with water/shower.

More
Less

N-Bromosuccinimide Price

Sigma-Aldrich
Product number
M55909
Product name
Methyl methacrylate
Purity
contains ≤30 ppm MEHQ as inhibitor, 99%
Packaging
1l
Price
$70
Updated
2024/03/01
Sigma-Aldrich
Product number
M55909
Product name
Methyl methacrylate
Purity
contains ≤30 ppm MEHQ as inhibitor, 99%
Packaging
2l
Price
$103
Updated
2024/03/01
Sigma-Aldrich
Product number
SAB1306524
Product name
ANTI-NEPRILYSIN(C-TERMINAL) antibody produced in rabbit
Purity
affinity isolated antibody, buffered aqueous solution
Packaging
400μl
Price
$481
Updated
2024/03/01
Sigma-Aldrich
Product number
8.00590
Product name
Methyl methacrylate
Purity
(stabilised) for synthesis
Packaging
100ML
Price
$43.2
Updated
2024/03/01
Sigma-Aldrich
Product number
8.00590
Product name
Methyl methacrylate
Purity
(stabilised) for synthesis
Packaging
1L
Price
$73.4
Updated
2024/03/01
More
Less

Methyl methacrylate Chemical Properties,Usage,Production

Description

Methyl methacrylate is an organic compound with the formula CH2=C(CH3)COOCH3. This colourless liquid, the methyl ester of methacrylic acid (MAA) is a monomer produced on a large scale for the production of poly(methyl methacrylate) (PMMA).

Chemical Properties

Methyl 2-methyl-2-propenoate has an acrid, penetrating odor. In another report this compound is reported to possess a sharp, fruity odor

Chemical Properties

Methyl methacrylate is a colorless liquid. Acrid, fruity odor. The odor threshold is 0.050.083 ppm

Chemical Properties

Methyl methacrylate is a methyl ester of methacrylic acid. It is a colourless, volatile liquid with an acrid fruity odour. It has a relatively high vapour pressure (4 kPa at 20°C), moderate water solubility (15.8 g/litre), and a low log octanol/water partition coefficient (Kow = 1.38) . Methyl methacrylate is typically 99.9% pure and contains small amounts of inhibitor to retard polymerization.

Physical properties

Clear, colorless liquid with a penetrating, fruity odor. An experimentally determined odor threshold concentration of 210 ppbv was reported by Leonardos et al. (1969). Experimentally determined detection and recognition odor threshold concentrations were 200 μg/m3 (49 ppbv) and 1.4 mg/m3 (340 ppbv), respectively (Hellman and Small, 1974).

Uses

Methyl methacrylatec is used in acrylic bone cements used in orthopedic surgery; in the production of acrylic polymers, polymethylmethacrylate and copolymers used in acrylic surface coatings; in the manufaeture of emulsion polymers; in the modification of unsaturated polyester resins; in the production of higher methacrylate, acrylic fibers, acrylic film, inks, radiation-polymerized impregnants for wood, and solvent-based adhesives and binders; as an impact modifier of PVC; in medicinal spray adhesives; in nonirritant bandage solvents; in dental technology as ceramic filler or cement; to coat corneal contact lenses; in intraocular lenses, artificial nails, and hearing aids; as a monomer for polymethaerylate resins; in the impregnation of concretc.

Uses

  1. Methyl methacrylate is a volatile synthetic chemical that is used principally in the production of cast acrylic sheet, acrylic emulsions, and moulding and extrusion resins.
  2. In the manufacture of methacrylate resins and plastics. Methyl methacrylate is transesterified into higher methacrylates such as n-butyl methacrylate or 2-ethylhexyl methacrylate.
  3. methyl methacrylate monomer is used in the production of methylmethacrylate polymers and copolymers, polymers and copolymers are also used in waterborne, solvent, and undissolved surface coatings, adhesives, sealants, leather and paper coatings, inks, floor polishes, textile finishes, dental prostheses, surgical bone cements, and leaded acrylic radiation shields and in the preparation of synthetic fingernails and orthotic shoe inserts. Methyl methacrylate is also used as a starting material to manufacture other esters of methacrylic acid.
  4. Granules for injection and extrusion blow moulding which for their outstanding optical clarity, weathering and scratch resistance are used in lighting, office equipment and electronics (cell phone displays and hi-fi equipment), building and construction (glazing and window frames), contemporary design (furniture, jewellery and tableware), cars and transportation (lights and instrument panels), health and safety (jars and test tubes) and household appliances (microwave oven doors and mixer bowls).
  5. Impact modifiers for clear rigid polyvinyl chloride.

Uses

The principal application, consuming approximately 80% of the MMA, is the manufacture of poly methyl methacrylate acrylic plastics (PMMA). Methyl methacrylate is also used for the production of the co-polymer methyl methacrylate-butadiene-styrene (MBS), used as a modifier for PVC. Another application is as cement used in total hip replacements as well as total knee replacements. Used as the "grout" by orthopedic surgeons to make the bone inserts fix into bone, it greatly reduces post-operative pain from the insertions but has a finite lifespan. Typically the lifespan of methyl methacrylate as bone cement is 20 years before revision surgery is required. Cemented implants are usually only done in elderly populations that require more immediate short term replacements. In younger populations, cementless implants are used because their lifespan is considerably longer. Also used in fracture repair in small exotic animal species using internal fixation.

Production Methods

The compound is manufactured by several methods, the principal one being the acetone cyanohydrin (ACH) route, using acetone and hydrogen cyanide as raw materials. The intermediate cyanohydrin is converted with sulfuric acid to a sulfate ester of the methacrylamide, methanolysis of which gives ammonium bisulfate and MMA. Although widely used, the ACH route coproduces substantial amounts of ammonium sulfate. Some producers start with an isobutylene or, equivalently, tert-butanol, which is sequentially oxidized first to methacrolein and then to methacrylic acid, which is then esterified with methanol. Propene can be carbonylated in the presence of acids to iso butyric acid, which undergoes subsequent dehydrogenation . The combined technologies afford more than 3 billion kilograms per year. MMA can also be prepared from methyl propionate and formaldehyde.

Production Methods

Methyl methacrylate (MMA) is the most important ester of methacrylic acid. It can be homo- and copolymerised to produce acrylic resins with good strength, transparency and with excellent weather resistance. The first commercial process for making MMA (1930's), the acetone cyanohydrin route, remains the predominant process in use today. In the acetone cyanohydrin route, acetone cyanohydrin reacts with sulfuric acid at low temperature to produce the sulfuric monoester of 2-hydroxy-2-methyl-propionamide, which forms methacrylamide sulphate after exposure to higher temperatures (100° - 140°C). The liquid phase is maintained by using an excess of 0.2 - 0.7 moles of 100% sulfuric acid. The first step of the reaction is strongly exothermic while the rearrangement of the sulfuric ester is endothermic.
During the synthesis of methacrylamide, a portion of the acetone cyanohydrin decomposes to carbon monoxide during the first part of the reaction. Additionally other by-products are formed and react due to the strength of the acid and high temperature in the second step. About 92 - 94% of the acetone cyanohydrin is converted to useful products and 6 - 8% is consumed in the formation of organic by-products (acetone, acetone sulphonates, olygomers, polymers, others). Methacrylamide sulphate is esterified with a mixture of water and methanol to form MMA and an aqueous solution of ammonium hydrogensulphate, sulfuric acid and the organic by-products. The ammonium hydrogensulphate is an unavoidable by-product of the reaction.

Definition

ChEBI: Methyl methacrylate is an enoate ester having methacrylic acid as the carboxylic acid component and methanol as the alcohol component. It has a role as an allergen and a polymerisation monomer. It is an enoate ester and a methyl ester. It is functionally related to a methacrylic acid.

Preparation

Prepared by the esterification of methacrylamide sulfate with methanol.

Aroma threshold values

Detection at 0.024 to 0.058 ppm (water); recognition at 0.7 to 1.4 mg/m3 (air); detection at 0.2 to 0.62 mg/m3.

Synthesis Reference(s)

Journal of the American Chemical Society, 70, p. 1153, 1948 DOI: 10.1021/ja01183a082
The Journal of Organic Chemistry, 33, p. 2525, 1968 DOI: 10.1021/jo01270a082

General Description

A clear colorless liquid. Slightly soluble in water and floats on water. Vapors heavier than air. Vapors irritate the eyes and respiratory system. Containers must be heavily insulated or shipped under refrigeration. An inhibitor such as hydroquinone, hydroquinone methyl ester and dimethyl t-butylphenol is added to keep the chemical from initiating polymerization. The chemical may polymerize exothermically if heated or contaminated with strong acid or base. If the polymerization takes place inside a container, the container may rupture violently. Used to make plastics.

Air & Water Reactions

Highly flammable. Very slightly soluble in water.

Reactivity Profile

Methyl methacrylate, may polymerize if contaminated or subjected to heat. If polymerization takes place in a container, the container is subject to violent rupture. Oxidizes readily in air to form unstable peroxides that may explode spontaneously [Bretherick 1979. p.151-154, 164]. Peroxides may also initiate exothermic polymierization of the bulk material [Bretherick 1979. p. 160]. Benzoyl peroxide was weighed into a beaker that had previously been rinsed with methyl methacrylate. The peroxide catalyzed polymerization of the methyl methacrylate and the build-up of heat ignited the remaining peroxide [MCA Case History 996. 1964].

Hazard

Flammable, dangerous fire risk, explosivelimits in air 2.1–12.5%. Eye and upper respiratorytract irritant, body weight effects, and pulmonaryedema. Questionable carcinogen.

Health Hazard

  1. Methyl methacrylate may cause slight eye irritation or moderate skin irritation. It is considered a skin sensitizer; allergic reactions may result from contact. Inhalation of vapor or mist can cause irritation of the nose, throat, and lungs and can be fatal in high concentrations. Prolonged or repeated overexposure has been reported to affect the kidneys, liver, gastrointestinal tract, nervous system and lung.
  2. Methyl methacrylate is moderately toxic to aquatic organisms on an acute basis. The bioconcentration potential (tendency to accumulate in the food chain) is low. If released to surface water, methyl methacrylate will readily biodegrade. A portion may evaporate to the air. It will not persist in the environment.
  3. Irritation of eyes, nose, and throat. Nausea and vomiting. Liquid may cause skin irritation.

Fire Hazard

Behavior in Fire: Vapor is heavier than air and may travel a considerable distance to a source of ignition and flash back. Containers may explode in fire or when heated because of polymerization.

Flammability and Explosibility

Flammable

Industrial uses

Initiators for methyl methacrylate polymerization include AIBN, dilauroyl peroxide (LPO), and 2,2'-Azobis[2-(2-imidazolin-2- yl)propane].

Safety Profile

Moderately toxic by inhalation and intraperitoneal routes. Mildly toxic by ingestion. Human systemic effects by inhalation: sleep effects, excitement, anorexia, and blood pressure decrease. Experimental teratogenic and reproductive effects. Mutation data reported. A skin and eye irritant. Questionable carcinogen with experimental tumorigenic data. A common air contaminant. A very dangerous fire hazard when exposed to heat or flame; can react with oxidizing materials. Explosive in the form of vapor when exposed to heat or flame. The monomer may undergo spontaneous, explosive polymerization. Reacts in air to form a heat-sensitive explosive product (explodes on evaporation at 6OOC). May ignite on contact with benzoyl peroxide. Potentially violent reaction with the polymerization initiators azoisobutyronitrile, dibenzoyl peroxide, di-tert-butyl peroxide, propionaldehyde. To fight fire, use foam, CO2, dry chemical. When heated to decomposition it emits acrid smoke and irritating fumes.

Potential Exposure

Virtually all of the methyl methacrylate monomer produced is used in the production of polymers, such as surface coating resins; plastics (Plexiglas and Lucite); ion exchange resins; and plastic dentures.

First aid

If this chemical gets into the eyes, remove anycontact lenses at once and irrigate immediately for at least15 min, occasionally lifting upper and lower lids. Seek medical attention immediately. If this chemical contacts theskin, remove contaminated clothing and wash immediatelywith soap and water. Seek medical attention immediately. Ifthis chemical has been inhaled, remove from exposure,begin rescue breathing (using universal precautions, including resuscitation mask) if breathing has stopped and CPR ifheart action has stopped. Transfer promptly to a medicalfacility. When this chemical has been swallowed, get medical attention. Give large quantities of water and inducevomiting. Do not make an unconscious person vomit.

Carcinogenicity

In several lifetime animal studies, there was no evidence that methyl methacrylate is carcinogenic.

Environmental Fate

Chemical/Physical. Polymerizes easily (Windholz et al., 1983). Methyl methacrylate undergoes nucleophilic attack by OH ions in water (hydrolysis) resulting in the formation of methacrylic acid and methanol (Kollig, 1993). Hydrolysis occurs at a rate of 171/M?h at 25 °C (Sharma and Sharma, 1970). No measurable hydrolysis was observed at 85.0 °C (pH 7) and 25 °C (pH 7.07). Hydrolysis half-lives of 9 and 134 min were observed at 66.0 °C (pH 9.86) and 25.0 °C (pH 11.3), respectively (Ellington et al., 1987).

storage

Methyl methacrylate is a reactive chemical that must be stored and handled with care. It is stable under recommended storage conditions. Heat can cause polymerization. Inhibitor is added to methyl methacrylate monomer to prevent polymerization. For the inhibitor to be effective, the oxygen concentration in the vapor space must be at least 5%. Store material in containers made of stainless steel, carbon steel, glass, or aluminum. Avoid contact with acids, bases, oxidizing agents, reducing agents, UV light (ultraviolet light, which is found in sunlight), free-radical initiators, and organic peroxides.

Shipping

UN1247 Methyl methacrylate monomer, stabilized, Hazard Class: 3; Labels: 3-Flammable liquid.

Purification Methods

Wash the ester twice with aqueous 5% NaOH (to remove inhibitors such as hydroquinone) and twice with water. Dry it with CaCl2, Na2CO3, Na2SO4 or MgSO4, then with CaH2 under nitrogen under reduced pressure. The distillate is stored at low temperatures and redistilled before use. Prior to distilling, inhibitors such as hydroquinone (0,004%), .-naphthylamine (0.2%) or di--naphthol are sometimes added. Also purify it by boiling with aqueous H3PO4 solution and finally with saturated NaCl solution. It is dried for 24hours over anhydrous CaSO4, distilled at 0.1mm Hg at room temperature and stored at -30o [Albeck et al. J Chem Soc, Faraday Trans 1 1 1488 1978]. [Beilstein 2 II 398, 2 III 1279, 2 IV 1519.]

Toxicity evaluation

The mitochondria are regarded as the main intracellular target of MMA. If isolated rat liver mitochondria are incubated with MMA, oxygen consumption increases. This is the result of an uncoupling of the mitochondrial respiratory chain, as seen from the expected influence on state 4 and state 3 respiration. State 4 respiration is stimulated. As has been reported for organic solvents, MMA attacks complex I of the respiratory chain close to the rotenonebinding site. This means that substrates which are oxidized in conjunction with nicotinamide adenine dinucleotide inhibit the flow of electrons and thus also ATP synthesis. Unlike classical uncouplers, MMA stimulates the Mg2+- dependent ATPase bound to the inner mitochondrial membrane. Structural changes in the inner membrane, as found with nonionic detergents, were observed by electron micro scopy. The release of enzymes indicates disintegration of the membrane.

Incompatibilities

Vapor may form explosive mixture with air. Reacts in air to form a heat-sensitive explosive product @ 60C. Incompatible with nitrates, oxidizers, peroxides, strong acids; strong alkalis; oxidizers, reducing agents; amines, moisture. Contact with benzoyl peroxide may cause ignition, fire and explosion. May polymerize if subjected to heat, polymerization catalysts e. g., azoisobutyronitrile, dibenzoyl peroxide; di-tert-butyl peroxide, propionaldehyde); strong oxidizers; or ultraviolet light. May contain an inhibitor, such as hydroquinone.

Waste Disposal

Consult with environmental regulatory agencies for guidance on acceptable disposal practices. Generators of waste containing this contaminant (≥100 kg/mo) must conform to EPA regulations governing storage, transportation, treatment, and waste disposal. Incineration may be allowed.

Methyl methacrylate Preparation Products And Raw materials

Raw materials

CARBON MONOXIDE Acetone cyanohydrin Ketone methacrylammonium hydrogen sulphate Isobutylene Methyl isobutyrate Sodium cyanide HYDROGEN CYANIDE Methanol Isobutyraldehyde Sulfuric acid

Preparation Products

Methyl 3-amino-4-methylthiophene-2-carboxylate METHYL 3-CHLORO-4-METHYLTHIOPHENE-2-CARBOXYLATE DIHYDROTHYMINE Leather lustering agent CC-2SH adhesive composite used in anterior teeth Poly(methyl methacrylate) 2,3-DIHYDROXYPROPYL METHACRYLATE Pressure sensitive adhesive 4-CHLORO-7-METHYLTHIENO[3,2-D]PYRIMIDINE Neoprene adhesive thickening agent PAE optical diskbase material modified PMMA copolymer binding agent for screen printing microdispersoid acrylate resin filling emulsion 3-CHLORO-4-METHYL-2-THIOPHENECARBOXYLIC ACID Procymidone THERMOPLASTIC ACRYLIC RESIN 7-Methylthieno[3,2-d]pyrimidin-4(3H)-one GD visible light curing composite resin 3-Methacryloxypropyltrimethoxysilane 2,2-DICHLORO-1-METHYLCYCLOPROPANAMINE carboxyl type cation exchange resin conductive coating-composite system of acrylic copolymer and cuprous iodide Bicalutamide 1-BENZYL-3-METHYL-4-PIPERIDONE Styrene-acrylic latex Poly(acrylic acid) Thymine
More
Less

Methyl methacrylate Suppliers

Americas 1 Argentina 1 Australia 5 Belgium 5 Brazil 1 Canada 9 China 349 Egypt 2 Europe 2 Finland 1 France 4 Germany 12 India 97 Indonesia 1 Italy 2 Japan 23 Malaysia 2 Mexico 2 Russia 3 Saudi Arabia 1 Singapore 4 Slovakia 1 South Korea 6 Spain 1 Switzerland 3 Thailand 1 The Netherlands 3 Turkey 1 United Arab Emirates 3 United Kingdom 16 United States 87 Global 649
Shandong chuangying chemical co., ltd
Tel
155-8990-1131; 15589901131
Email
2235633711@qq.com
Country
China
ProdList
162
Advantage
58
Shanghai Aladdin Bio-Chem Technology Co.,LTD
Tel
400-400-6206333 18521732826
Fax
021-50323701
Email
market@aladdin-e.com
Country
China
ProdList
25003
Advantage
65
Shandong Jinyueyuan New Material Co. Ltd
Tel
18615186228
Email
3404852510@qq.com
Country
China
ProdList
446
Advantage
58
Shandong le Li New Materials Co. , Ltd.
Tel
18906359122
Email
258225957@qq.com
Country
China
ProdList
53
Advantage
58
Jinan Zhiyuancheng Chemical Co. LTD
Tel
13287786355 13287786355
Email
913870783@qq.com
Country
China
ProdList
379
Advantage
58
Mingwei (Shandong) Supply Chain Management Co., Ltd
Tel
15553101303 15553101303
Email
mingweichemical@163.com
Country
China
ProdList
494
Advantage
58
26/2000 Shanghai Fantanxi Bio-chemical Technology Co. , Ltd.
Tel
19251267229
Email
764796998@qq.com
Country
China
ProdList
1550
Advantage
58
Jinan Chuangshi Chemical Co., LTD
Tel
18854143038
Email
3686420496@qq.com
Country
China
ProdList
331
Advantage
58
shandongxinhenghuagongyouxiangongsi
Tel
1526-9160602 15269160602
Email
15269160602@163.com
Country
China
ProdList
472
Advantage
58
Meryer (Shanghai) Chemical Technology Co., Ltd.
Tel
021-61259108 18621169109
Fax
86-21-61259102
Email
market03@meryer.com
Country
China
ProdList
40228
Advantage
62
Alfa Aesar
Tel
400-6106006
Fax
021-67582001/03/05
Email
saleschina@alfa-asia.com
Country
China
ProdList
30123
Advantage
84
TCI (Shanghai) Development Co., Ltd.
Tel
021-67121386
Fax
021-67121385
Email
Sales-CN@TCIchemicals.com
Country
China
ProdList
24529
Advantage
81
Beijing dtftchem Technology Co., Ltd.
Tel
010-60275820 13031183356
Fax
010-60270825
Email
elainezt@sina.com
Country
China
ProdList
1390
Advantage
62
Energy Chemical
Tel
021-021-58432009 400-005-6266
Fax
021-58436166
Email
sales8178@energy-chemical.com
Country
China
ProdList
44688
Advantage
61
Beijing Ouhe Technology Co., Ltd
Tel
010-82967028 13552068683
Fax
+86-10-82967029
Email
2355560935@qq.com
Country
China
ProdList
12390
Advantage
60
Shanghai Hanhong Scientific Co.,Ltd.
Tel
021-54306202 13764082696
Email
info@hanhongsci.com
Country
China
ProdList
42958
Advantage
64
Beijing Isomersyn Technology CO;LTD
Tel
010-82954736 13391601435
Email
sales@isomersyn.com
Country
China
ProdList
3295
Advantage
57
Sichuan Kulinan Technology Co., Ltd
Tel
400-1166-196 18981987031
Fax
028-84555506 800101999
Email
cdhxsj@163.com
Country
China
ProdList
11707
Advantage
57
China Langchem Inc.
Tel
0086-21-58956006
Fax
0086-21-58956100
Country
China
ProdList
7811
Advantage
57
Tianjin heowns Biochemical Technology Co., Ltd.
Tel
400 638 7771
Email
sales@heowns.com
Country
China
ProdList
14435
Advantage
57
Sinopharm Chemical Reagent Co,Ltd.
Tel
86-21-63210123
Fax
86-21-63290778 86-21-63218885
Email
sj_scrc@sinopharm.com
Country
China
ProdList
9815
Advantage
79
Nanjing Vital Chemical Co., Ltd.
Tel
Please Send Email 18652950785
Fax
025-87193546
Email
chemweiao@163.com
Country
China
ProdList
4378
Advantage
65
Explovisual Technology Incorporation
Tel
+86 (519) 8829-2061
Fax
+86 (519) 8829-2061
Email
explovisual@hotmail.com
Country
China
ProdList
296
Advantage
60
Spectrum Chemical Manufacturing Corp.
Tel
021-021-021-67601398-809-809-809 15221380277
Fax
021-57711696
Email
marketing_china@spectrumchemical.com
Country
China
ProdList
9658
Advantage
60
Chengdu Ai Keda Chemical Technology Co., Ltd.
Tel
4008-755-333 18080918076
Fax
028-86757656
Email
800078821@qq.com
Country
China
ProdList
9718
Advantage
55
Shanghai civi chemical technology co.,Ltd
Tel
86-21-34053660
Fax
86-21-34053661
Email
sale@labgogo.com
Country
China
ProdList
9865
Advantage
52
Thermo Fisher Scientific
Tel
800-810-5118
Fax
+86-10-84193589
Email
cnchemical@thermofisher.com
Country
China
ProdList
17770
Advantage
75
Beijing innoChem Science & Technology Co.,Ltd.
Tel
400-810-7969 010-59572699
Fax
010-59572688
Email
ningzi.li@inno-chem.com.cn
Country
China
ProdList
6134
Advantage
55
9ding chemical ( Shanghai) Limited
Tel
4009209199
Fax
86-021-52271987
Email
sales@9dingchem.com
Country
China
ProdList
22514
Advantage
55
Shanghai Yolne Chemical Co., Ltd.
Tel
021-62960152
Fax
021-52212593
Email
934678158@qq.com
Country
China
ProdList
9899
Advantage
55
Beijing Universal Century Technology Co., Ltd.
Tel
400-8706899
Fax
400-8706899
Email
hysj_bj.com
Country
China
ProdList
3583
Advantage
55
Shanghai Meishui Chemical Technology Co., Ltd
Tel
021-60549325 18616193163
Fax
021-33250306
Country
China
ProdList
4526
Advantage
56
Mei Lan Industrial (Shanghai) Co., Ltd.
Tel
021-58958189
Fax
021-58957967
Email
wouchina@126.com
Country
China
ProdList
2666
Advantage
55
Shanghai ideal Industrial Co., Ltd.
Tel
021-58957966 18930537195
Fax
021-60899437
Email
wouchina@126.com
Country
China
ProdList
3027
Advantage
58
Chengdu HuaXia Chemical Reagent Co. Ltd
Tel
400-1166-196 13458535857
Fax
QQ：800101999
Email
cdhxsj@163.com
Country
China
ProdList
13350
Advantage
58
GuangTuo Chemical (Shanghai) Co., Ltd.
Tel
021-60899189-8001 18918189673
Fax
021-60899304
Email
gtchem@126.com
Country
China
ProdList
2656
Advantage
58
Shanghai Macklin Biochemical Co.,Ltd.
Tel
15221275939 15221275939
Fax
021-50706099
Email
shenlinxing@macklin.cn
Country
China
ProdList
16166
Advantage
55
Shanghai Kewel Chemical Co., Ltd.
Tel
021-64609169 18901607656
Fax
021-64609160
Email
greensnown@163.com
Country
China
ProdList
9906
Advantage
50
SHANGHAI BANGCHENG CHEMICAL Co.,Ltd.
Tel
021-69106960 13701823733
Fax
021-69106780
Email
13701823733@163.com
Country
China
ProdList
4772
Advantage
60
Qingdao RENAS Polymer Material Co.,Ltd.
Tel
0532-0532-86867058 18562606086
Fax
0532-86867058
Email
sales@qdrenas.com
Country
China
ProdList
128
Advantage
50
Shanghai YouPeng Chemical Co. Ltd.
Tel
021-69005955 13701776567
Fax
021-69005775
Email
youpengchem@163.com
Country
China
ProdList
4295
Advantage
56
Shanghai TongYuan Chemical Co., Ltd.
Tel
021-021-69182866 13701855675
Fax
021-69182022
Email
tongyuanchem@126.com
Country
China
ProdList
4321
Advantage
58
Shanghai Kaisai Chemical Co., Ltd
Tel
021-33516722 13701817765
Fax
021-33516776
Email
kaisaichem@163.com
Country
China
ProdList
4742
Advantage
58
Chengdu RunZeBenTu Chemical Co., Ltd
Tel
13096311329 028-88469284 616445927
Fax
028-88469284
Email
616445927@qq.com
Country
China
ProdList
2874
Advantage
50
Shanghai LanRun Chemical Co., Ltd.
Tel
021-69515658 ; 69515628 13701998368
Fax
021-69515998
Email
longrunchem@163.com
Country
China
ProdList
3912
Advantage
50
Shanghai Rolead Chemical Technology Co., Ltd.
Tel
021-69992220 13701886816
Fax
021-69992237
Email
roleadchem@163.com
Country
China
ProdList
4750
Advantage
50
Shanghai Kangtuo Chemical Co., Ltd.
Tel
021-69185552 13701777608
Fax
021-69186006
Email
kangtuochem@163.com
Country
China
ProdList
4360
Advantage
55
Chizhou Kailong Import and Export Trade Co., Ltd.
Tel
Fax
-
Email
xg01_gj@163.com
Country
China
ProdList
9484
Advantage
50
Sigma-Aldrich
Tel
021-61415566 800-8193336
Email
orderCN@merckgroup.com
Country
China
ProdList
51456
Advantage
80
Zhengzhou KeYulong chemical products Co., Ltd
Tel
17319789407
Fax
0371-53335504
Email
Keyulongchem@163.com
Country
China
ProdList
1993
Advantage
55
More
Less

View Lastest Price from Methyl methacrylate manufacturers

ChemFine International Co.,Ltd.
Product
Methyl methacrylate (MMA) 80-62-6
Price
US $1.26-1.15/kg
Min. Order
3000kg
Purity
99% min
Supply Ability
17200 kg
Release date
2024-07-15
Hebei Weibang Biotechnology Co., Ltd
Product
Methyl methacrylate 80-62-6
Price
US $10.00/kg
Min. Order
1kg
Purity
99.5%
Supply Ability
100 TON
Release date
2024-10-30
Qingdao RENAS Polymer Material Co., Ltd.
Product
Methyl Methacrylate 80-62-6
Price
US $0.00/kg
Min. Order
20kg
Purity
99.0%
Supply Ability
20 tons
Release date
2024-07-02

80-62-6, Methyl methacrylateRelated Search:

Methanol 2-Hydroxypropyl methacrylate Methylparaben Paraquat dichloride Methyl acetate 2-Hydroxyethyl methacrylate Acetonitrile Methyl acrylate Basic Violet 1 Kresoxim-methyl Glycidyl methacrylate POLYMETHACRYLATE Methacrylic acid Acrylic acid Methacrylamide Methacryloyl chloride 2-Aminoethyl methacrylate hydrochloride 2-Methoxyethyl methacrylate

  • Methyl 2-methylacrylate
  • Methyl alpha-methylacrylate
  • Methyl ester of 2-methyl-2-propenoic acid
  • Methyl methylacrylate
  • Methyl2-methylacrylate
  • Methyl2-methylpropenate
  • Methyl-alpha-methacrylate
  • methylalpha-methylacrylate
  • Methylester kyseliny methakrylove
  • methylesterkyselinymethakrylove
  • Methylmetacrylate
  • Methylmethacrylaat
  • Methyl-methacrylat
  • methylmethacrylatemonomer,inhibited
  • rcrawastenumberu162
  • MMA
  • METHYL METACRYLAT
  • METHYL METHACRYLATE, 1X1ML, MEOH, 1000UG /ML
  • METHYL METHACRYLATE STABILIZED &
  • METHYL METHACRYLATE, STAB. WITH 0.0025% HYDROQUINONE
  • METHYL METHACRYLATEGC STANDARD
  • Methylmethacrylate,99%,stab.withca100ppmhydroquinone
  • Methyl Methacrylate-2-methyl-D3
  • methyl methacrylate solution
  • MONOMETHYLMETHACRYLATE
  • METHYLMETHACRYLICACID
  • Methacrylsuremethylester
  • 2-Propenoic acid, 2-methyl-, methyl ester (I,T)
  • Methyl methacrylate (I, T)
  • METHYL METHACRYLATE , STABILIZED WITH CA 100PPM HYDROQUINONE
  • MethylMethacrylateCertified
  • MethylMethacryalate(Stabilised)
  • MethylMethacrylate>99%
  • Methyl methacrylate, 99%, stab. with hydroquinone
  • Methyl Methacrylate (stabilized with 6-tert-Butyl-2,4-xylenol)
  • Methyl-2-methylprop-2-enoate, Methyl methacrylate
  • Atriopeptidase
  • Common acute lymphocytic leukemia antigen
  • MMA,Methyl methacrylate
  • MMA Methacrylic Acid Methyl Ester
  • Methyl methacrylate, 99.8%, stabilized
  • 2-Methylpropenoicacidmethylest
  • METHACRYLIC ACID METHYL ESTER
  • METHYL A-METHYLACRYLATE
  • METHYL 2-METHYL-2-PROPENOATE
  • METHYL 2-METHYLPROPENOATE
  • monocite Methacrylate monomer
  • 2-(methoxycarbonyl)-1-propene
  • 2-Methyl-2-propenoic acid methyl ester
  • 2-methylpropenoicacid,methylester
  • 2-Methylpropenoicacidmethylester
  • 2-Propenoicacid,2-methyl-,methylester
  • 2-METHYLACRYLIC ACID METHYL ESTER
  • METHYL METHACRYLATE
  • METHYL METHACRYLATE, MONOMER
  • 2-Methyl-2-propenoic acid methyl
  • Methyl isopropenoate
  • Methyl methacrylate, 99%, stab.