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Source: The Open Library

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1Synthesis of acrylic esters by transesterification, 1967

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“Synthesis of acrylic esters by transesterification, 1967” Metadata:

  • Title: ➤  Synthesis of acrylic esters by transesterification, 1967
  • Author:
  • Language: English
  • Number of Pages: Median: 95
  • Publisher: Noyes Development Corp.
  • Publish Date:
  • Publish Location: Park Ridge, N.J

“Synthesis of acrylic esters by transesterification, 1967” Subjects and Themes:

Edition Identifiers:

  • The Open Library ID: OL5544195M
  • Online Computer Library Center (OCLC) ID: 1861620
  • Library of Congress Control Number (LCCN): 67022365

Access and General Info:

  • First Year Published: 1967
  • Is Full Text Available: No
  • Is The Book Public: No
  • Access Status: No_ebook

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2Methyl methacrylate

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Book's cover

“Methyl methacrylate” Metadata:

  • Title: Methyl methacrylate
  • Authors:
  • Language: English
  • Number of Pages: Median: 40
  • Publisher: World Health Organization
  • Publish Date:
  • Publish Location: Geneva

“Methyl methacrylate” Subjects and Themes:

Edition Identifiers:

Access and General Info:

  • First Year Published: 1998
  • Is Full Text Available: No
  • Is The Book Public: No
  • Access Status: No_ebook

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Wiki

Source: Wikipedia

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Poly(methyl methacrylate)

Poly(methyl methacrylate) (PMMA) is a synthetic polymer derived from methyl methacrylate. It is a transparent thermoplastic, used as an engineering plastic

Methacrylate

Methacrylates are derivatives of methacrylic acid. These derivatives are mainly used to make poly(methyl methacrylate) and related polymers. Monomers

Methyl methacrylate

manufacture of other methacrylates. These derivatives include ethyl methacrylate (EMA), butyl methacrylate (BMA) and 2-ethyl hexyl methacrylate (2-EHMA). Methacrylic

Röhm GmbH (Darmstadt)

"LiMA" technology stands for "Leading in Methacrylates" and involves a new production method for methacrylates. This production is designed to be more

(Hydroxyethyl)methacrylate

"Hydroxyalkyl methacrylates: Kinetic investigations of radical polymerizations of pure 2-hydroxyethyl methacrylate and 2, 3-dihydroxypropyl methacrylate and the

Glycidyl methacrylate

Glycidyl methacrylate (GMA) is an ester of methacrylic acid and glycidol. Containing both an epoxide and an acrylate group, the molecule is bifunctional

Bis-GMA

Bis-GMA (bisphenol A-glycidyl methacrylate) is a resin commonly used in dental composite, dental sealants. and dental cement. It is the diester derived

Butyl methacrylate

Butyl methacrylate is the organic compound with the formula C4H9O2CC(CH3)=CH2. A colorless liquid, it is a common monomer for the preparation of methacrylate

Methacrylic acid

as a precursor to its esters, especially methyl methacrylate (MMA), and to poly(methyl methacrylate) (PMMA). In the most common route, methacrylic acid

Ethyl methacrylate

and butyl methacrylates have respective acute LD50s of 10 and 20 g/kg (oral, rat); a linear extrapolation suggests that ethyl methacrylate would have