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    Dodecyl Methacrylate

    ACTIVE PHARMA INGREDIENTS

    PharmaCompass
    $ API Ref.Price (USD/KG) : 5Xls

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    2D Structure
    Also known as: 142-90-5, Lauryl methacrylate, Dodecyl 2-methylacrylate, 2-propenoic acid, 2-methyl-, dodecyl ester, N-dodecyl methacrylate, Metazene
    Molecular Formula
    C16H30O2
    Molecular Weight
    254.41  g/mol
    InChI Key
    GMSCBRSQMRDRCD-UHFFFAOYSA-N
    FDA UNII
    B6L83074BZ
    1 2D Structure

    2D Structure

    2 Identification
    2.1 Computed Descriptors
    2.1.1 IUPAC Name
    dodecyl 2-methylprop-2-enoate
    2.1.2 InChI
    InChI=1S/C16H30O2/c1-4-5-6-7-8-9-10-11-12-13-14-18-16(17)15(2)3/h2,4-14H2,1,3H3
    2.1.3 InChI Key
    GMSCBRSQMRDRCD-UHFFFAOYSA-N
    2.1.4 Canonical SMILES
    CCCCCCCCCCCCOC(=O)C(=C)C
    2.2 Other Identifiers
    2.2.1 UNII
    B6L83074BZ
    2.3 Synonyms
    2.3.1 MeSH Synonyms

    1. Dma, Methacrylate

    2. Lauryl Methacrylate

    2.3.2 Depositor-Supplied Synonyms

    1. 142-90-5

    2. Lauryl Methacrylate

    3. Dodecyl 2-methylacrylate

    4. 2-propenoic Acid, 2-methyl-, Dodecyl Ester

    5. N-dodecyl Methacrylate

    6. Metazene

    7. Dodecyl 2-methylprop-2-enoate

    8. Dodecyl 2-methyl-2-propenoate

    9. Methacrylic Acid, Dodecyl Ester

    10. Sipomer Lma

    11. Lama

    12. Ageflex Fm 246

    13. Methacrylic Acid, Lauryl Ester

    14. Ge 410 (methacrylate)

    15. Laurylester Kyseliny Methakrylove

    16. Laurylmethacrylate

    17. Nsc 5188

    18. Ge 410

    19. Sr 313

    20. N-lauryl Methacrylate

    21. Acrylic Acid, 2-methyl-, Dodecyl Ester

    22. B6l83074bz

    23. Nsc-5188

    24. Dodecyl Methacrylate (stabilized With Mehq)

    25. Dsstox_cid_7103

    26. Dsstox_rid_78311

    27. Dsstox_gsid_27103

    28. Caswell No. 521

    29. Dodecyl-2-methylacrylate

    30. Cas-142-90-5

    31. Hsdb 5417

    32. Einecs 205-570-6

    33. Epa Pesticide Chemical Code 053101

    34. Brn 1708160

    35. Laurylester Kyseliny Methakrylove [czech]

    36. Unii-b6l83074bz

    37. Ai3-08765

    38. Ageflex Fm-12

    39. 1-dodecyl Methacrylate

    40. Methacrylic Acid Dodecyl

    41. 2-methyl-2-propenoic Acid, Dodecyl Ester

    42. 1-dodecanol Methacrylate

    43. Ec 205-570-6

    44. Dodecyl 2-methylacrylate #

    45. Schembl14995

    46. Wln: 12ovyu1

    47. Methacrylic Acid Lauryl Ester

    48. Methacrylic Acid Dodecyl Ester

    49. Chembl1903701

    50. Dtxsid4027103

    51. Nsc5188

    52. Lauryl Methacrylate [inci]

    53. Tox21_201903

    54. Tox21_303316

    55. Mfcd00008972

    56. Zinc38141474

    57. N-dodecyl Methacrylate [hsdb]

    58. Akos015903634

    59. Cs-w012588

    60. Methyl-2-propenoic Acid, Dodecyl Ester

    61. Lauryl Methacrylate(5cp(25 Degrees C))

    62. Ncgc00164408-01

    63. Ncgc00164408-02

    64. Ncgc00257059-01

    65. Ncgc00259452-01

    66. 170292-57-6

    67. As-76599

    68. Propenoic Acid, 2-methyl-, Dodecyl Ester

    69. Db-042652

    70. Dodecyl Ester Of 2-methyl-2-propenoic Acid

    71. Ft-0625575

    72. M0083

    73. Dodecyl Methacrylate, (stabilized With Mehq)

    74. Lauryl Methacrylate, Purum, >=95.0% (gc)

    75. E75856

    76. A807982

    77. J-007716

    78. Q3395664

    79. Lauryl Methacrylate, Contains 500 Ppm Mehq As Inhibitor, 96%

    2.4 Create Date
    2005-03-26
    3 Chemical and Physical Properties
    Molecular Weight 254.41 g/mol
    Molecular Formula C16H30O2
    XLogP37.2
    Hydrogen Bond Donor Count0
    Hydrogen Bond Acceptor Count2
    Rotatable Bond Count13
    Exact Mass254.224580195 g/mol
    Monoisotopic Mass254.224580195 g/mol
    Topological Polar Surface Area26.3 Ų
    Heavy Atom Count18
    Formal Charge0
    Complexity221
    Isotope Atom Count0
    Defined Atom Stereocenter Count0
    Undefined Atom Stereocenter Count0
    Defined Bond Stereocenter Count0
    Undefined Bond Stereocenter Count0
    Covalently Bonded Unit Count1
    4 Pharmacology and Biochemistry
    4.1 Metabolism/Metabolites

    Small quantities of methacrylates may readily be metabolized by saponification into the alcohol and methacrylic acid. The latter may form an acetyl-coenzyme A derivative, which then enters the normal lipid metabolism. /Methacrylates/

    Clayton, G. D. and F. E. Clayton (eds.). Patty's Industrial Hygiene and Toxicology: Volume 2A, 2B, 2C: Toxicology. 3rd ed. New York: John Wiley Sons, 1981-1982., p. 2298

    Acrylates and methacrylates are detoxified predominantly via conjugation with glutathione via the Michael addition reaction or glutathione-S-transferase. They are also likely to be hydrolyzed via carboxylesterases. The lower molecular weight esters are rapidly metabolized and eliminated, therefore, will not likely cause cumulative toxicity. /Methacrylates/

    Bingham, E.; Cohrssen, B.; Powell, C.H.; Patty's Toxicology Volumes 1-9 5th ed. John Wiley & Sons. New York, N.Y. (2001)., p. V6 600