Glycidyl methacrylate (CAS 106-91-2) — formula C7H10O3, molecular weight 142.06 g/mol.
| CAS Number | 106-91-2 |
|---|---|
| Molecular Formula | C7H10O3 |
| Molecular Weight | 142.06 g/mol |
| Melting Point | freezing pt: -41.5 °C |
| Boiling Point | 372 °F at 760 mmHg (NTP, 1992) |
| LogP | 0.96 |
| Applications | Uses: Chemical intermediate for polymers, monomer and diluent in epoxy resin formulations, [HSDB] Used in Japan as an intermediate for resins and other chemicals, Also used in emulsions for impregnating paper and textiles, in paint coatings, and adhesive applications, [OECD SIDS: Glycidyl methacrylate - 1999], Pulp and Paper Processing [Category: Industry], Painting (Pigments, Binders, and Biocides) [Category: Paint], Working with Glues and Adhesives [Category: Other], Textiles (Printing, Dyeing, or Finishing) [Category: Industry], CHEM INT FOR POLYMERS, MONOMER & DILUENT IN EPOXY RESIN FORMULATIONS., In hydrogel lenses., In BIS-GMA dental resin., Adhesion promotion, crosslinking comonomer (acrylic, vinyl resins), Industry Uses: Filler, Not Known or Reasonably Ascertainable, Surface modifier, Other, Monomers, Methods of Manufacturing: REACTION OF METHACRYLIC ACID WITH GLYCIDOL, The methacrylates can be synthesized by catalytic oxidation of isobutylene and subsequent esterification with the appropriate alcohol, or by reacting acetone with hydrocyanic acid and subsequent esterification in sulfuric acid with the appropriate alcohol., Methacrylic esters, Epichlorohydrin + methacrylic acid (esterification), Formulations, Preparations: Grades or purity: Technical: 92%, Inhibitor of polymerization: Hydroquinone monomethyl ether: 50 ppm, U.S. Production: 2023: 10, 000, 000 - <50, 000 lb, 2022: 1, 000 - <5, 2021: 10, 2020: 10, (1972) GREATER THAN 4.54X10+5 G, (1975) GREATER THAN 4.54X10+5 G, U.S. Imports: (1983) 1.36X10+9 g, Acrylates & Acrylic Acid, General Manufacturing Information: Plastics Material and Resin Manufacturing, Paint and Coating Manufacturing, All Other Chemical Product and Preparation Manufacturing, Asphalt Paving, Roofing, and Coating Materials Manufacturing, 2-Propenoic acid, 2-methyl-, 2-oxiranylmethyl ester: ACTIVE, METHYL METHACRYLATE, AND IN GENERAL THE METHACRYLIC ESTERS, POLYMERIZE MUCH LESS READILY THAN THE CORRESPONDING ORDINARY ACRYLATES. NONE THE LESS, THEY ARE STABILIZED BY ADDING HYDROQUINONE OR PYROGALLOL, PARTICULARLY IN THE PRESENCE OF METALLIC COPPER., METHACRYLATES |
Documented applications: Uses: Chemical intermediate for polymers, monomer and diluent in epoxy resin formulations, [HSDB] Used in Japan as an intermediate for resins and other chemicals, Also used in emulsions for impregnating paper and textiles, in paint coatings, and adhesive applications, [OECD SIDS: Glycidyl methacrylate - 1999], Pulp and Paper Processing [Category: Industry], Painting (Pigments, Binders, and Biocides) [Category: Paint], Working with Glues and Adhesives [Category: Other], Textiles (Printing, Dyeing, or Finishing) [Category: Industry], CHEM INT FOR POLYMERS, MONOMER & DILUENT IN EPOXY RESIN FORMULATIONS., In hydrogel lenses., In BIS-GMA dental resin., Adhesion promotion, crosslinking comonomer (acrylic, vinyl resins), Industry Uses: Filler, Not Known or Reasonably Ascertainable, Surface modifier, Other, Monomers, Methods of Manufacturing: REACTION OF METHACRYLIC ACID WITH GLYCIDOL, The methacrylates can be synthesized by catalytic oxidation of isobutylene and subsequent esterification with the appropriate alcohol, or by reacting acetone with hydrocyanic acid and subsequent esterification in sulfuric acid with the appropriate alcohol., Methacrylic esters, Epichlorohydrin + methacrylic acid (esterification), Formulations, Preparations: Grades or purity: Technical: 92%, Inhibitor of polymerization: Hydroquinone monomethyl ether: 50 ppm, U.S. Production: 2023: 10, 000, 000 - <50, 000 lb, 2022: 1, 000 - <5, 2021: 10, 2020: 10, (1972) GREATER THAN 4.54X10+5 G, (1975) GREATER THAN 4.54X10+5 G, U.S. Imports: (1983) 1.36X10+9 g, Acrylates & Acrylic Acid, General Manufacturing Information: Plastics Material and Resin Manufacturing, Paint and Coating Manufacturing, All Other Chemical Product and Preparation Manufacturing, Asphalt Paving, Roofing, and Coating Materials Manufacturing, 2-Propenoic acid, 2-methyl-, 2-oxiranylmethyl ester: ACTIVE, METHYL METHACRYLATE, AND IN GENERAL THE METHACRYLIC ESTERS, POLYMERIZE MUCH LESS READILY THAN THE CORRESPONDING ORDINARY ACRYLATES. NONE THE LESS, THEY ARE STABILIZED BY ADDING HYDROQUINONE OR PYROGALLOL, PARTICULARLY IN THE PRESENCE OF METALLIC COPPER., METHACRYLATES.
Glycidyl methacrylate is a chemical compound with CAS registry number 106-91-2 and molecular formula C7H10O3 (molecular weight 142.06 g/mol).
CAS number: 106-91-2
Its molecular formula C7H10O3 comprises 7 C, 10 H, 3 O atoms.
Also known as: Glycidyl methacrylate · 甲基丙烯酸缩水甘油酯
The CAS registry number of Glycidyl methacrylate is 106-91-2.
Molecular formula C7H10O3, molecular weight 142.06 g/mol.
It is also registered under: Glycidyl methacrylate, 甲基丙烯酸缩水甘油酯.
Recorded applications: Uses: Chemical intermediate for polymers, monomer and diluent in epoxy resin formulations, [HSDB] Used in Japan as an intermediate for resins and other chemicals, Also used in emulsions for impregnating paper and textiles, in paint coatings, and adhesive applications, [OECD SIDS: Glycidyl methacrylate - 1999], Pulp and Paper Processing [Category: Industry], Painting (Pigments, Binders, and Biocides) [Category: Paint], Working with Glues and Adhesives [Category: Other], Textiles (Printing, Dyeing, or Finishing) [Category: Industry], CHEM INT FOR POLYMERS, MONOMER & DILUENT IN EPOXY RESIN FORMULATIONS., In hydrogel lenses., In BIS-GMA dental resin., Adhesion promotion, crosslinking comonomer (acrylic, vinyl resins), Industry Uses: Filler, Not Known or Reasonably Ascertainable, Surface modifier, Other, Monomers, Methods of Manufacturing: REACTION OF METHACRYLIC ACID WITH GLYCIDOL, The methacrylates can be synthesized by catalytic oxidation of isobutylene and subsequent esterification with the appropriate alcohol, or by reacting acetone with hydrocyanic acid and subsequent esterification in sulfuric acid with the appropriate alcohol., Methacrylic esters, Epichlorohydrin + methacrylic acid (esterification), Formulations, Preparations: Grades or purity: Technical: 92%, Inhibitor of polymerization: Hydroquinone monomethyl ether: 50 ppm, U.S. Production: 2023: 10, 000, 000 - <50, 000 lb, 2022: 1, 000 - <5, 2021: 10, 2020: 10, (1972) GREATER THAN 4.54X10+5 G, (1975) GREATER THAN 4.54X10+5 G, U.S. Imports: (1983) 1.36X10+9 g, Acrylates & Acrylic Acid, General Manufacturing Information: Plastics Material and Resin Manufacturing, Paint and Coating Manufacturing, All Other Chemical Product and Preparation Manufacturing, Asphalt Paving, Roofing, and Coating Materials Manufacturing, 2-Propenoic acid, 2-methyl-, 2-oxiranylmethyl ester: ACTIVE, METHYL METHACRYLATE, AND IN GENERAL THE METHACRYLIC ESTERS, POLYMERIZE MUCH LESS READILY THAN THE CORRESPONDING ORDINARY ACRYLATES. NONE THE LESS, THEY ARE STABILIZED BY ADDING HYDROQUINONE OR PYROGALLOL, PARTICULARLY IN THE PRESENCE OF METALLIC COPPER., METHACRYLATES.
Independent reference data for Glycidyl methacrylate (CAS 106-91-2), compiled from public chemistry databases.
| CAS Registry Number | 106-91-2 |
|---|---|
| PubChem CID | 7837 |
| Molecular formula | C7H10O3 |
| Molecular weight | 142.06 g/mol |
| IUPAC name | oxiran-2-ylmethyl 2-methylprop-2-enoate |
| InChIKey | VOZRXNHHFUQHIL-UHFFFAOYSA-N |
| UNII (FDA) | R8WN29J8VF |
| ChEBI ID | CHEBI:132844 |
| Molecular Weight | 142.15 |
|---|---|
| XLogP3 | 0.8 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 3 |
| Rotatable Bond Count | 4 |
| Exact Mass | 142.062994177 |
| Monoisotopic Mass | 142.062994177 |
| Topological Polar Surface Area | 38.8 |
| Heavy Atom Count | 10 |
| Boiling Point | 372 °F at 760 mmHg (NTP, 1992) |
|---|---|
| Boiling Point | 189 °C |
| Melting Point | freezing pt: -41.5 °C |
| Flash Point | 181 °F (NTP, 1992) |
| Flash Point | 84 °C (Tag open cup) |
| Solubility | 5 to 10 mg/mL at 68 °F (NTP, 1992) |
| Density | 1.07 g/cu cm @ 25 °C |
| Vapor Pressure | 3.15 [mmHg] |
| LogP | 0.96 |
| Viscosity | 5.481 cP at 70 °F |
GLYCIDYL METHACRYLATE; 106-91-2; 2,3-Epoxypropyl methacrylate; Glycidol methacrylate; SY-Monomer G; Blemmer G; Acriester G; Blemmer GMA; Light Ester G; Methacrylic acid, 2,3-epoxypropyl ester; 2-((Methacryloxy)methyl)oxirane; DTXSID0025361; 2-Propenoic acid, 2-methyl-, oxiranylmethyl ester; Glycidyl alpha-methylacrylate; CP 105; Glycidyl alpha-methyl acrylate
| Regulatory & Food Contact | FDA Inventory of Food Contact Substances Listed in 21 CFR: FCS FDA Inventory of Effective Food Contact Substance (FCS) Noti: FCS Glycidyl methacrylate (CAS Reg. No. 106-91-2) As a monomer in the manufacture of acrylic copolymers complying with 21 CFR 175.300 (b)(3)(xx) for use as comp |
|---|---|
| GHS notification summary | 0.1% (1 / 1165) |
| GHS notification summary | 0.1% (1 / 1165) |
|---|---|
| Reported hazard statements | H302, H311, H314, H317, H318, H335, H341, H350 |
H302: Harmful if swallowed [Warning Acute toxicity, oral]
H311: Toxic in contact with skin [Danger Acute toxicity, dermal]
Glycidyl methacrylate is identified by CAS 106-91-2, molecular formula C7H10O3 and molecular weight 142.06 g/mol. UNII R8WN29J8VF; ChEBI 132844; InChIKey VOZRXNHHFUQHIL-UHFFFAOYSA-N. Boiling Point: 372 °F at 760 mmHg (NTP, 1992); Boiling Point: 189 °C; Melting Point: freezing pt: -41.5 °C.
Source: PubChem / Wikidata; the batch COA governs where values differ.
Supplier: Jinan Shenghe Chemical Co., Ltd.
中文页面: 甲基丙烯酸缩水甘油酯