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GLYCEROL 1,3-DIMETHACRYLATE, also known as GDMA, is an organic chemical compound that serves as a cross-linking monomer in the formulation of dental composites. It is composed of carbon, hydrogen, and oxygen atoms and is instrumental in enhancing the mechanical and physical properties of dental materials, such as hardness and durability.
Used in Dental Industry:
GLYCEROL 1,3-DIMETHACRYLATE is used as a cross-linking monomer for improving the mechanical and physical properties of dental materials, such as increasing their hardness and durability. It contributes to the formulation of dental composites that are essential for creating dental materials with enhanced performance characteristics.
GLYCEROL 1,3-DIMETHACRYLATE is also used as a resin material in restorative dental procedures, providing a strong and stable bond to the tooth structure. This ensures the longevity and effectiveness of dental restorations, such as fillings and crowns.
However, it is important to note that GDMA is a potent sensitizer and can cause allergic reactions in some individuals. Therefore, proper safety precautions must be taken when handling and using this chemical in dental applications to minimize the risk of adverse reactions.

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  • 1830-78-0 Structure
  • Basic information

    1. Product Name: GLYCEROL 1,3-DIMETHACRYLATE
    2. Synonyms: 2-hydroxy-1,3-propanediyl bismethacrylate;GLYCEROL DIMETHACRYLATE, TECH., 85%, MIX TURE OF ISOMERS;2-Hydroxy 1-3,dimethacryloxy propane;glycerol dimethacrylate, mixture of isomers;2-Hydroxy-1,3-propandiylbismethacrylat;1,3-Dimethacryloyloxy-2-hydroxypropane;GLYCERIN DIMETHACRYLATE;1,3-Bis(methacryloyloxy)-2-propanol (stabilized with MEHQ)
    3. CAS NO:1830-78-0
    4. Molecular Formula: C11H16O5
    5. Molecular Weight: 228.24
    6. EINECS: 217-388-4
    7. Product Categories: monomer;Diacrylates & Dimethacrylates;Functional Materials;Reagent for High-Performance Polymer Research;Acrylic Monomers;C10 to C11Monomers;Carbonyl Compounds;Esters;Polyfunctional Acrylics
    8. Mol File: 1830-78-0.mol
  • Chemical Properties

    1. Melting Point: -33°C
    2. Boiling Point: 120 °C1 mm Hg(lit.)
    3. Flash Point: >230 °F
    4. Appearance: /
    5. Density: 1.12 g/mL at 25 °C(lit.)
    6. Vapor Pressure: 3.28E-05mmHg at 25°C
    7. Refractive Index: n20/D 1.472(lit.)
    8. Storage Temp.: 2-8°C
    9. Solubility: N/A
    10. PKA: 12.49±0.20(Predicted)
    11. CAS DataBase Reference: GLYCEROL 1,3-DIMETHACRYLATE(CAS DataBase Reference)
    12. NIST Chemistry Reference: GLYCEROL 1,3-DIMETHACRYLATE(1830-78-0)
    13. EPA Substance Registry System: GLYCEROL 1,3-DIMETHACRYLATE(1830-78-0)
  • Safety Data

    1. Hazard Codes: Xi
    2. Statements: 36/37/38
    3. Safety Statements: 26-36
    4. WGK Germany: 1
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 1830-78-0(Hazardous Substances Data)

1830-78-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1830-78-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,8,3 and 0 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1830-78:
(6*1)+(5*8)+(4*3)+(3*0)+(2*7)+(1*8)=80
80 % 10 = 0
So 1830-78-0 is a valid CAS Registry Number.
InChI:InChI=1/C11H16O5/c1-7(2)10(13)15-5-9(12)6-16-11(14)8(3)4/h9,12H,1,3,5-6H2,2,4H3

1830-78-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name [2-hydroxy-3-(2-methylprop-2-enoyloxy)propyl] 2-methylprop-2-enoate

1.2 Other means of identification

Product number -
Other names Bis(methacryloyloxy)propanol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1830-78-0 SDS

1830-78-0Relevant articles and documents

Vanillin-based resin for use in composite applications

Stanzione Iii, Joseph F.,Sadler, Joshua M.,La Scala, John J.,Reno, Kaleigh H.,Wool, Richard P.

, p. 2346 - 2352 (2012)

Lignin is an abundant, renewable material that has the potential to yield valuable, low molecular weight, single aromatic chemicals when strategically depolymerized. In order to generate a highly bio-based thermoset for use in polymer composites, a lignin-derived chemical, vanillin, was methacrylated in a two-step, one-pot synthesis to produce a vinyl ester resin (87 cP at 25 °C) with a 1:1 mole ratio of a mono-functional monomer, methacrylated vanillin, to cross-linking agent, glycerol dimethacrylate. The synthetic scheme was solventless, required little catalyst and moderate reaction temperatures while generating no by-products. Upon resin curing, a hard, transparent thermoset with a broad glass transition, Tg = 155 °C (based on the tan δ maximum), and a temperature of maximum decomposition rate, Tmax, of 426 °C was produced. Overall, a potentially 100% bio-based thermoset was synthesized possessing comparable thermo-gravimetric and thermo-mechanical properties to commercial vinyl ester-based thermosets.

MANUFACTURING METHOD OF ESTER COMPOUND

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Paragraph 0028-0031, (2016/02/18)

A manufacturing method of an ester compound includes reacting, in a nonpolar solvent, a compound including, in one molecule of the compound, an ester structure and an alcoholic hydroxyl group with a compound that abstracts a proton from the alcoholic hydroxyl group.

CARDANOL GLYCIDYL ETHER DERIVATIVES

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Paragraph 0078, (2015/11/27)

Methacrylated cardanol glycidyl ethers, diglycidyl ethers, intermediates and derivatives thereof are described herein. Compositions and polymers made with such compounds as well as methods of preparation thereof are also described. For example, compounds of Formulas: wherein n, R1, R2, R3, R4, R5, and R6 can each represent various different entities are described in the present disclosure.

Hydroxy functional acrylate and methacrylate monomers prepared via lipase-catalyzed transacylation reactions

Popescu, Dragos,Hoogenboom, Richard,Keul, Helmut,Moeller, Martin

experimental part, p. 80 - 89 (2010/08/20)

Candida antarctica lipase B (CAL-B, Novozyme 435) catalyzes the transacylation of methyl acrylate and methyl methacrylate with diols and triols in 2-methyl-2-butanol at 50 °C. Under the experimental conditions, up to 70 mol% of the acyl donor methyl acrylate was converted. Methyl methacrylate is the less efficient acyl donor (up to 60 mol%) due to the higher sterical hindrance in the enzymatic transacylation. Under the reaction conditions high yields of the mono-acylated products are obtained, which contain minor amounts of bis(meth)acrylates. In addition it was observed that Novozyme 435 catalyzes regioselectively the acylation of the primary hydroxyl groups. In comparison with the chemical catalyzed route no selectivity was observed for unsubstituted diols. For substituted diols more mono-acylated product was formed in the lipase-catalyzed reaction than in the chemical catalyzed reaction.

Reactivity of some carboxylic acids in reactions with some epoxides in the presence chromium (III) ethanoate

Bukowska, Agnieszka,Bukowski, Wiktor

, p. 234 - 237 (2013/09/06)

Reactivities have been compared of acetic, acrylic, and methacrylic acid in reactions with epichlorohydrin, phenylglycidyl ether, glycidyl acetate, and glycidyl methacrylate carried in the presence of chromium (III) ethanoate. The acid reactivities changed differently with respect to the oxirane series. The effect of solvents on the reactions of acids with epichlorohydrin has also been observed.

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