Methyl acrylate(MA) - ≥99%(GC), contains ≤100 ppm MEHQ as stabilizer , CAS No.96-33-3

CAS: 96-33-3 Cat. No.: M100033 Summenformel: C₄H₆O₂ Molekulargewicht: 86.09 Beilstein Registry Number: 605396 EG-Nummer: 202-500-6

GRADE & PURITY ≥99%(GC), contains ≤100 ppm MEHQ as stabilizer

Synonyms

A0145 | Acrylate de methyle [French] | Methylacrylaat [Dutch] | METHYL ACRYLATE (IARC) | F0001-2293 | Metilacrilato [Italian] | 2-propenoic acid methyl ester | Methyl acrylate, 99%, contains <=100 ppm monomethyl ether hydroquinone as inhibitor | Methylacr

Storage

Store at 2-8°C,Protected from light

Shipped In

Wet ice,FedEx DG Service

Übersicht

Methyl acrylate is an acrylic monomer. It is useful in the preparation of polymers having rigid, flexible, ionic, nonionic, hydrophobic, or hydrophilic properties. Mechanism of the copolymerization of ethylene and α-olefins with methyl acrylate has been studied. Heck reaction of iodobenzene with methyl acrylate in the presence of triethylamine and sodium carbonate has been reported. The reversible addition fragmentation chain transfer (RAFT) bulk polymerization of methyl acrylate using 1-phenylethyl dithiobenzoate and 2-(2-cyanopropyl) dithiobenzoate (RAFT agents) has been studied. Reactive intermediates formed during the Heck reaction of methyl acrylate have been characterized by NMR spectroscopy.
Methyl acrylate was used in the preparation of poly(methyl acrylate) elastomers. It was also used in the synthesis of α,ω-dicarboxylic acid esters.

Specifications

Synonyme

A0145 | Acrylate de methyle [French] | Methylacrylaat [Dutch] | METHYL ACRYLATE (IARC) | F0001-2293 | Metilacrilato [Italian] | 2-propenoic acid methyl ester | Methyl acrylate, 99%, contains <=100 ppm monomethyl ether hydroquinone as inhibitor | Methylacr

Spezifikationen & Reinheit

≥99%(GC), contains ≤100 ppm MEHQ as stabilizer

Storage

Store at 2-8°C,Protected from light

Verschickt in

Wet ice,FedEx DG Service

Dieses Produkt erfordert Kühlkettenversand. Grundversand und andere Economy-Optionen sind nicht verfügbar.

Reinheit

≥99%(GC)

Namen und Kennungen

Pubchem Sid

488180374

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/488180374

Kanonisches Lächeln

COC(=O)C=C

IUPAC Name

methyl prop-2-enoate

InChIKey

BAPJBEWLBFYGME-UHFFFAOYSA-N

INCHI

1S/C4H6O2/c1-3-4(5)6-2/h3H,1H2,2H3

Isomere SMILES

COC(=O)C=C

WGK Deutschland

2

RTECS

AT2800000

UN-Nummer

1919

Verpackungsgruppe

II

Molekulargewicht

86.09

Beilstein

605396

Reaxy-Rn

605396

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=605396&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • Klasse Carboxylic acids and derivatives
      • Subclass Acrylic acids and derivatives

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Klasse: Carboxylic acids and derivatives
• Subclass: Acrylic acids and derivatives
• Intermediate Tree Nodes: Not available
• Direct Parent: Acrylic acid esters
• Alternative Parents: Methyl esters Enoate esters Monocarboxylic acids and derivatives Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Acrylic acid ester - Alpha,beta-unsaturated carboxylic ester - Enoate ester - Methyl ester - Carboxylic acid ester - Monocarboxylic acid or derivatives - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aliphatic acyclic compound
• Beschreibung: This compound belongs to the class of organic compounds known as acrylic acid esters. These are organic compounds containing and ester acrylic acid (CH2=CHC(=O)OH).
• External Descriptors: enoate ester

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Zugehörige Ziele (menschlich)

TYMS Tclin Thymidylate synthase (1651 Activities)

Discover Target: TYMS

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

SLC6A3 Tclin Dopamine transporter (10535 Activities)

Discover Target: SLC6A3

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Zugehörige Ziele (nicht menschlich)

Aspergillus niger (16508 Activities)

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Candida albicans (78123 Activities)

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Mucor mucedo (338 Activities)

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Wirkungsmechanismen

Chemische und physikalische Eigenschaften

• Löslichkeit: Miscible with water
• Empfindlichkeit: Light sensitive.
• Brechungsindex: 1.401
• Flammpunkt (°F): 26.6 °F
• Flammpunkt (°C): -3℃
• Siedepunkt (°C): 80°C
• Schmelzpunkt (°C): -75°C
• Molekulargewicht: 86.090 g/mol
• XLogP3: 0.800
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 2
• Exact Mass: 86.0368 Da
• Monoisotopic Mass: 86.0368 Da
• Topological Polar Surface Area: 26.300 Ų
• Heavy Atom Count: 6
• Formal Charge: 0
• Complexity: 65.900
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1