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2451-62-9

  • Product Name:Tris(Epoxy propyl) Isocyanurate
  • Molecular Formula:C12H15 N3 O6
  • Purity:99%
  • Molecular Weight:297.268
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Product Details

  • CasNo: 2451-62-9
  • Molecular Formula: C12H15 N3 O6
  • Appearance: white crystalline solid
  • Quality manufacturer supply Tris(Epoxy propyl) Isocyanurate 2451-62-9 in stock with high standard

    • Molecular Formula:C12H15 N3 O6
    • Molecular Weight:297.268
    • Appearance/Colour:white crystalline solid 
    • Vapor Pressure:3.56E-10mmHg at 25°C 
    • Melting Point:95-98 °C 
    • Refractive Index:1.635 
    • Boiling Point:501.1 °C at 760 mmHg 
    • PKA:-2.44±0.20(Predicted) 
    • Flash Point:256.9 °C 
    • PSA:103.59000 
    • Density:1.625 g/cm3 
    • LogP:-2.63190 

    1,3,5-Triglycidyl isocyanurate(Cas 2451-62-9) Usage

    Industrial Application

    1,3,5-triglycidyl isocyanurate (TGIC) is a white powder or granular solid and is normally sold under the trade name ARALDITE PT810R or TEPIC G R. As a tri-functional epoxy monomer, TGIC is used in large scale as curing agent for powder coatings or for cross-linking elastomers. Rosin acids of natural origin may also be cured with TGIC for versatile applications. TGIC has also been used for pharmaceutical purposes, in membranes, for curing intelligent gels or liquid crystal elastomers. Especially, this curing agent has been widely used in dry powder coating for over 40 years.

    Health Toxicity

    It has been known that TGIC is toxic by inhalation and if swallowed. It is a severe eye irritant, and a mild skin and nasal irritant, although it has the potential to cause skin sensitisation in people which can lead to severe skin rashes. Exposure to TGIC in powder paints may cause not only contact dermatitis, but also occupational asthma. Kidney damage has also been observed in rats repeatedly exposed to TGIC by oral dosing, and damage to the developing sperm cells has been observed in mice repeatedly exposed to TGIC orally and by inhalation. There is an evidence that exposure of males to TGIC produces genetic changes in the sperm which may lead to heritable effects in the offspring. There is cause for concern that these effects could occur in humans, so that TGIC has been classified in the EU as a Category 2 mutagen. Exposures to TGIC during manufacturing procedures have been identified as hazardous to workers.

    General Description

    White crystalline solid.

    Air & Water Reactions

    Insoluble in water.

    Reactivity Profile

    Epoxides are highly reactive. They polymerize in the presence of catalysts or when heated. These polymerization reactions can be violent. Compounds in this group react with acids, bases, and oxidizing and reducing agents. They react, possibly violently with water in the presence of acid and other catalysts.

    Fire Hazard

    Flash point data for 1,3,5-Triglycidyl isocyanurate are not available; however, 1,3,5-Triglycidyl isocyanurate is probably combustible.

    Flammability and Explosibility

    Nonflammable

    Contact allergens

    Triglycidyl isocyanurate is a triazine epoxy compound used as a resin hardener in polyester powder paints, in the plastics industry, resin molding systems, inks, and adhesives. Occupational contact dermatitis can occur in people producing this chemical, in those producing the powder coat paint, and in sprayers. Respiratory symptoms have been observed.

    InChI:InChI=1/C12H15N3O6/c16-10-13(1-7-4-19-7)11(17)15(3-9-6-21-9)12(18)14(10)2-8-5-20-8/h7-9H,1-6H2

    2451-62-9 Relevant articles

    -

    Price,Schroll

    , p. 2005 (1967)

    -

    Synthesis method of high-purity tris (glycidyl) isocyanurate

    -

    Paragraph 0027-0059, (2021/07/14)

    The invention discloses a synthesis meth...

    Low-chlorine electronic-grade TGIC and preparation method thereof

    -

    Paragraph 0023-0046, (2021/08/21)

    The invention belongs to the technical f...

    Preparation method of triglycidyl isocyanurate

    -

    Paragraph 0038-0051, (2021/02/06)

    The invention relates to a preparation m...

    Method for synthesizing TGIC and coproducing ECH from dichloropropanol

    -

    Paragraph 0033; 0035-0037; 0039-0041; 0043-0045; 0047-0049, (2020/11/23)

    The invention provides a method for synt...

    2451-62-9 Process route

    1,3,5-tris-(3-chloro-2-hydroxy-propyl)-[1,3,5]triazinane-2,4,6-trione
    7423-53-2

    1,3,5-tris-(3-chloro-2-hydroxy-propyl)-[1,3,5]triazinane-2,4,6-trione

    teroxirone
    2451-62-9,28825-96-9,240408-78-0

    teroxirone

    Conditions
    Conditions Yield
    With calcium oxide; at 50 - 60 ℃; for 4h;
    98.92%
    With sodium hydroxide; In methanol; at 15 ℃; for 1.5h; Temperature; Solvent; Large scale;
    With potassium hydroxide; In water; at 35 - 50 ℃; for 4h; Temperature; Reagent/catalyst;
    sodium isocyanate
    917-61-3

    sodium isocyanate

    epichlorohydrin
    106-89-8,24969-06-0,13403-37-7

    epichlorohydrin

    teroxirone
    2451-62-9,28825-96-9,240408-78-0

    teroxirone

    Conditions
    Conditions Yield
    With dihydrogen peroxide; benzyl bromide; In dimethyl sulfoxide; at 20 - 70 ℃; for 4h; Reagent/catalyst; Solvent; Temperature;
    85%

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      1,3,5-tris-(3-chloro-2-hydroxy-propyl)-[1,3,5]triazinane-2,4,6-trione

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    CAS:128-37-0

    Purity:99%

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