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Home › Product Catalog › 1,3,5-Triazine-2,4,6(1H,3H,5H)-trione,1,3,5-tris(2-oxiranylmethyl)-, homopolymer

1,3,5-Triazine-2,4,6(1H,3H,5H)-trione,1,3,5-tris(2-oxiranylmethyl)-, homopolymer

CAS 28825-96-9C12H15N3O6MW 297.26

1,3,5-Triazine-2,4,6(1H,3H,5H)-trione,1,3,5-tris(2-oxiranylmethyl)-, homopolymer (CAS 28825-96-9) — formula C12H15N3O6, molecular weight 297.26; category organic chemicals.

Product Overview

CAS Number28825-96-9
Molecular FormulaC12H15N3O6
Molecular Weight297.26
Melting Point203 to 208 °F (NTP, 1992)
Boiling Point> 240 °C, decomposition
LogP-1.5
ApplicationsUses: Used in powder coatings containing less than 5% TGIC, [ACGIH] Occupational asthma and allergic contact dermatitis reported in workers manufacturing thermosetting paints, [Reference #1] Causes allergic contact dermatitis in screen-printing workers handling UV-cured inks, [Adams, p. 467], Painting (Pigments, Binders, and Biocides) [Category: Paint], Plastic Composites Manufacturing [Category: Industry], Silk-Screen Printing [Category: Other], Crosslinking agent in polymer synthesis, additive in plastic, rubber, and adhesives, hardener in polyester powder coatings, in protective coatings of electronic devices, in top-coated and solder-resistant inks., The main use of triglycidyl isocyanurate is as a three-dimensional cross-linking or curing agent in polyester powder coatings (paints). ...Triglycidyl isocyanurate is also used in solder "mask" inks in the printed circuit board industry., Industry Uses: Intermediate, Hardener, Adhesion, cohesion promoter, Not Known or Reasonably Ascertainable, Chemical reaction regulator, Monomers, Consumer Uses: Hardener, Methods of Manufacturing: ... obtained by reacting cyanuric acid with epichlorohydrin., Improved process for the preparation and separation of the alpha and beta-forms by crystallization: M. Budnowski, United States of America patent 3300490 (1967 to Henkel & Cie.). Preparation of the (R, R, R) and (S, S, S) isomers: H. Ikeda et al., United States of America patent 6605717 (2003 to Nissan Chem. Ind.)., Reaction of CA, cyanuric acid, with epichlorohydrin in alkaline dioxane solution gives tris(3-chloro-2-hydroxypropyl)isocyanurate. This material can be converted into the commercial product, tris(2, 3-epoxypropyl)isocyanurate ... by dehydrohalogenation with alkali., Formulations, Preparations: Exists as a mixture of two pairs of diastereomer racemates, designated alpha and beta, that are separable on the basis of their solubility properties., ... Manufactured and supplied as the technical grades TEPIC and Araldite PT810. Technical-grade triglycidyl isocyanurate is a mixture of two diastereomers, alpha and beta., U.S. Production: 2023: 2, 500, 000 - <4, 000, 000 lb, 2022: 10, 000 - <25, 2021: 8, 000 - <10, 2020: 5, 000 - <7, Non-confidential 2016 Chemical Data Reporting (CDR) information on the production and use of chemicals manufactured or imported into the United States. Chemical: Triglycidyl isocyanurate:, Table: National Aggregate Production Volume (pounds) [Table#6801], General Manufacturing Information: Electrical Equipment, Appliance, and Component Manufacturing, Transportation Equipment Manufacturing, Miscellaneous Manufacturing, Furniture and Related Product Manufacturing, Paint and Coating Manufacturing, 1, 3, 5-Triazine-2, 4, 6(1H, 3H, 5H)-trione, 5-tris(2-oxiranylmethyl)-: ACTIVE, ... In the manufacture of powder coatings, triglycidyl isocyanurate granules are mixed with other ingredients, the mix is then melted and extruded as a brittle sheet, chipped, and packaged. Generally, the particle size of 90-95% of the powder coating is >10 um. Powder coatings usually contain 4-10% triglycidyl isocyanurate and are sprayed onto metal objects by an electrostatic process. The coated metal objects are then treated in an oven to a temperature of about 200 °C. This heating causes the powder coatings to melt, flow, and chemically cross-link. The coatings are durable and resist ultraviolet damage, as a result, they are typically used in outdoor applications. Triglycidyl isocyanurate is also used in solder "mask" inks in the printed circuit board industry. The two-part inks contain approximately 60% triglycidyl isocyanurate in the hardener component. The inks are applied by curtain coating, electrostatic spraying, or screen printing. The coated circuit board is finally passed through an oven at 150 °C to complete the curing.
CategoryOrganic Chemicals

Applications

Documented applications: Uses: Used in powder coatings containing less than 5% TGIC, [ACGIH] Occupational asthma and allergic contact dermatitis reported in workers manufacturing thermosetting paints, [Reference #1] Causes allergic contact dermatitis in screen-printing workers handling UV-cured inks, [Adams, p. 467], Painting (Pigments, Binders, and Biocides) [Category: Paint], Plastic Composites Manufacturing [Category: Industry], Silk-Screen Printing [Category: Other], Crosslinking agent in polymer synthesis, additive in plastic, rubber, and adhesives, hardener in polyester powder coatings, in protective coatings of electronic devices, in top-coated and solder-resistant inks., The main use of triglycidyl isocyanurate is as a three-dimensional cross-linking or curing agent in polyester powder coatings (paints). ...Triglycidyl isocyanurate is also used in solder "mask" inks in the printed circuit board industry., Industry Uses: Intermediate, Hardener, Adhesion, cohesion promoter, Not Known or Reasonably Ascertainable, Chemical reaction regulator, Monomers, Consumer Uses: Hardener, Methods of Manufacturing: ... obtained by reacting cyanuric acid with epichlorohydrin., Improved process for the preparation and separation of the alpha and beta-forms by crystallization: M. Budnowski, United States of America patent 3300490 (1967 to Henkel & Cie.). Preparation of the (R, R, R) and (S, S, S) isomers: H. Ikeda et al., United States of America patent 6605717 (2003 to Nissan Chem. Ind.)., Reaction of CA, cyanuric acid, with epichlorohydrin in alkaline dioxane solution gives tris(3-chloro-2-hydroxypropyl)isocyanurate. This material can be converted into the commercial product, tris(2, 3-epoxypropyl)isocyanurate ... by dehydrohalogenation with alkali., Formulations, Preparations: Exists as a mixture of two pairs of diastereomer racemates, designated alpha and beta, that are separable on the basis of their solubility properties., ... Manufactured and supplied as the technical grades TEPIC and Araldite PT810. Technical-grade triglycidyl isocyanurate is a mixture of two diastereomers, alpha and beta., U.S. Production: 2023: 2, 500, 000 - <4, 000, 000 lb, 2022: 10, 000 - <25, 2021: 8, 000 - <10, 2020: 5, 000 - <7, Non-confidential 2016 Chemical Data Reporting (CDR) information on the production and use of chemicals manufactured or imported into the United States. Chemical: Triglycidyl isocyanurate:, Table: National Aggregate Production Volume (pounds) [Table#6801], General Manufacturing Information: Electrical Equipment, Appliance, and Component Manufacturing, Transportation Equipment Manufacturing, Miscellaneous Manufacturing, Furniture and Related Product Manufacturing, Paint and Coating Manufacturing, 1, 3, 5-Triazine-2, 4, 6(1H, 3H, 5H)-trione, 5-tris(2-oxiranylmethyl)-: ACTIVE, ... In the manufacture of powder coatings, triglycidyl isocyanurate granules are mixed with other ingredients, the mix is then melted and extruded as a brittle sheet, chipped, and packaged. Generally, the particle size of 90-95% of the powder coating is >10 um. Powder coatings usually contain 4-10% triglycidyl isocyanurate and are sprayed onto metal objects by an electrostatic process. The coated metal objects are then treated in an oven to a temperature of about 200 °C. This heating causes the powder coatings to melt, flow, and chemically cross-link. The coatings are durable and resist ultraviolet damage, as a result, they are typically used in outdoor applications. Triglycidyl isocyanurate is also used in solder "mask" inks in the printed circuit board industry. The two-part inks contain approximately 60% triglycidyl isocyanurate in the hardener component. The inks are applied by curtain coating, electrostatic spraying, or screen printing. The coated circuit board is finally passed through an oven at 150 °C to complete the curing..

Technical Profile

What this product is

1,3,5-Triazine-2,4,6(1H,3H,5H)-trione,1,3,5-tris(2-oxiranylmethyl)-, homopolymer is a carbon-based organic compound with CAS registry number 28825-96-9 and molecular formula C12H15N3O6 (molecular weight 297.26), belonging to the organic chemicals segment of chemical raw materials.

Identification

CAS number: 28825-96-9

Its molecular formula C12H15N3O6 comprises 12 C, 15 H, 3 N, 6 O atoms.

Also known as: 1,3,5-Triazine-2,4,6(1H,3H,5H)-trione,1,3,5-tris(2-oxiranylmethyl)-, homopolymer · 1,3,5-三嗪-2,4,6(1H,3H,5H)-三酮,1,3,5-三(2-环氧乙烷基甲基)-,均聚物

Category: organic chemicals

Frequently Asked Questions

What is the CAS number of 1,3,5-Triazine-2,4,6(1H,3H,5H)-trione,1,3,5-tris(2-oxiranylmethyl)-, homopolymer?

The CAS registry number of 1,3,5-Triazine-2,4,6(1H,3H,5H)-trione,1,3,5-tris(2-oxiranylmethyl)-, homopolymer is 28825-96-9.

What is the molecular formula and molecular weight of 1,3,5-Triazine-2,4,6(1H,3H,5H)-trione,1,3,5-tris(2-oxiranylmethyl)-, homopolymer?

Molecular formula C12H15N3O6, molecular weight 297.26.

What other names is 1,3,5-Triazine-2,4,6(1H,3H,5H)-trione,1,3,5-tris(2-oxiranylmethyl)-, homopolymer known by?

It is also registered under: 1,3,5-Triazine-2,4,6(1H,3H,5H)-trione,1,3,5-tris(2-oxiranylmethyl)-, homopolymer, 1,3,5-三嗪-2,4,6(1H,3H,5H)-三酮,1,3,5-三(2-环氧乙烷基甲基)-,均聚物.

What are the documented applications of 1,3,5-Triazine-2,4,6(1H,3H,5H)-trione,1,3,5-tris(2-oxiranylmethyl)-, homopolymer?

Recorded applications: Uses: Used in powder coatings containing less than 5% TGIC, [ACGIH] Occupational asthma and allergic contact dermatitis reported in workers manufacturing thermosetting paints, [Reference #1] Causes allergic contact dermatitis in screen-printing workers handling UV-cured inks, [Adams, p. 467], Painting (Pigments, Binders, and Biocides) [Category: Paint], Plastic Composites Manufacturing [Category: Industry], Silk-Screen Printing [Category: Other], Crosslinking agent in polymer synthesis, additive in plastic, rubber, and adhesives, hardener in polyester powder coatings, in protective coatings of electronic devices, in top-coated and solder-resistant inks., The main use of triglycidyl isocyanurate is as a three-dimensional cross-linking or curing agent in polyester powder coatings (paints). ...Triglycidyl isocyanurate is also used in solder "mask" inks in the printed circuit board industry., Industry Uses: Intermediate, Hardener, Adhesion, cohesion promoter, Not Known or Reasonably Ascertainable, Chemical reaction regulator, Monomers, Consumer Uses: Hardener, Methods of Manufacturing: ... obtained by reacting cyanuric acid with epichlorohydrin., Improved process for the preparation and separation of the alpha and beta-forms by crystallization: M. Budnowski, United States of America patent 3300490 (1967 to Henkel & Cie.). Preparation of the (R, R, R) and (S, S, S) isomers: H. Ikeda et al., United States of America patent 6605717 (2003 to Nissan Chem. Ind.)., Reaction of CA, cyanuric acid, with epichlorohydrin in alkaline dioxane solution gives tris(3-chloro-2-hydroxypropyl)isocyanurate. This material can be converted into the commercial product, tris(2, 3-epoxypropyl)isocyanurate ... by dehydrohalogenation with alkali., Formulations, Preparations: Exists as a mixture of two pairs of diastereomer racemates, designated alpha and beta, that are separable on the basis of their solubility properties., ... Manufactured and supplied as the technical grades TEPIC and Araldite PT810. Technical-grade triglycidyl isocyanurate is a mixture of two diastereomers, alpha and beta., U.S. Production: 2023: 2, 500, 000 - <4, 000, 000 lb, 2022: 10, 000 - <25, 2021: 8, 000 - <10, 2020: 5, 000 - <7, Non-confidential 2016 Chemical Data Reporting (CDR) information on the production and use of chemicals manufactured or imported into the United States. Chemical: Triglycidyl isocyanurate:, Table: National Aggregate Production Volume (pounds) [Table#6801], General Manufacturing Information: Electrical Equipment, Appliance, and Component Manufacturing, Transportation Equipment Manufacturing, Miscellaneous Manufacturing, Furniture and Related Product Manufacturing, Paint and Coating Manufacturing, 1, 3, 5-Triazine-2, 4, 6(1H, 3H, 5H)-trione, 5-tris(2-oxiranylmethyl)-: ACTIVE, ... In the manufacture of powder coatings, triglycidyl isocyanurate granules are mixed with other ingredients, the mix is then melted and extruded as a brittle sheet, chipped, and packaged. Generally, the particle size of 90-95% of the powder coating is >10 um. Powder coatings usually contain 4-10% triglycidyl isocyanurate and are sprayed onto metal objects by an electrostatic process. The coated metal objects are then treated in an oven to a temperature of about 200 °C. This heating causes the powder coatings to melt, flow, and chemically cross-link. The coatings are durable and resist ultraviolet damage, as a result, they are typically used in outdoor applications. Triglycidyl isocyanurate is also used in solder "mask" inks in the printed circuit board industry. The two-part inks contain approximately 60% triglycidyl isocyanurate in the hardener component. The inks are applied by curtain coating, electrostatic spraying, or screen printing. The coated circuit board is finally passed through an oven at 150 °C to complete the curing..

Which category does 1,3,5-Triazine-2,4,6(1H,3H,5H)-trione,1,3,5-tris(2-oxiranylmethyl)-, homopolymer belong to?

Category: Organic Chemicals.

PubChem Public Data

Independent reference data for 1,3,5-Triazine-2,4,6(1H,3H,5H)-trione,1,3,5-tris(2-oxiranylmethyl)-, homopolymer (CAS 28825-96-9), compiled from public chemistry databases.

Registry identifiers across databases

CAS 号28825-96-9
PubChem CID17142
分子式C12H15N3O6
IUPAC 名称1,3,5-tris(oxiran-2-ylmethyl)-1,3,5-triazinane-2,4,6-trione
UNII(FDA)58P91Z020D

Computed descriptors

Molecular Weight297.26
XLogP3-1.5
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count6
Rotatable Bond Count6
Exact Mass297.09608521
Monoisotopic Mass297.09608521
Topological Polar Surface Area98.5
Heavy Atom Count21

Physicochemical values on record

Boiling Point> 240 °C, decomposition
Boiling PointBP: 210 °C at 0.2 mm Hg
Melting Point203 to 208 °F (NTP, 1992)
Melting Point95 °C
Melting PointMP: 203 to 208 °F
Melting Point203-208 °F
SolubilityIn water, 9-10.5 g/L at 25 °C, pH 5-8
SolubilityIn water, <1 mg/mL at 68 °F
SolubilityIn acetone, 1 g/L at 20 °C
SolubilityWater < 1 (mg/mL)

Synonyms and trade names

Triglycidyl isocyanurate; 2451-62-9; 1,3,5-Triglycidyl isocyanurate; TGIC; Glycidyl isocyanurate; Tris(2,3-epoxypropyl)isocyanurate; Tris(epoxypropyl) isocyanurate; Tri(epoxypropyl)isocyanurate; XB 2615; DTXSID4026262; Tris(2-epoxypropyl) isocyanurate; Tris(epoxypropyl)isocyanurate; N,N',N''-Triglycidyl isocyanurate; 1,3,5-Triglycidyl-s-triazinetrione; NSC 296934; s-Triazine-2,4,6(1H,3H,5H)-trione, tris(2,3-epoxypropyl)-

Regulatory listings held on file

法规与食品接触FDA 21 CFR 中列出的食品接触物质清单:FCS

GHS hazard classification

已通报的危害声明H301, H317, H318, H331, H340, H373, H412, H402

What the public record says

1,3,5-三嗪-2,4,6(1H,3H,5H)-三酮,1,3,5-三(2-环氧乙烷基甲基)-,均聚物 · CAS 28825-96-9 · C12H15N3O6. UNII 58P91Z020D. Boiling Point: > 240 °C, decomposition; Boiling Point: BP: 210 °C at 0.2 mm Hg; Melting Point: 203 to 208 °F (NTP, 1992).

Source: PubChem / Wikidata; the batch COA governs where values differ.

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