Cas no 17832-16-5 (Triallyl 1,3,5-Benzenetricarboxylate)

Triallyl 1,3,5-Benzenetricarboxylate is a trifunctional monomer characterized by its three allyl ester groups attached to a benzene core. This structure imparts high reactivity in polymerization processes, particularly in crosslinking applications, due to the presence of multiple unsaturated bonds. The compound is commonly utilized in the synthesis of thermosetting resins, coatings, and adhesives, where it enhances mechanical strength and thermal stability. Its symmetrical aromatic backbone contributes to improved rigidity and chemical resistance in cured materials. The product is also valued for its compatibility with various radical-initiated polymerization systems, making it a versatile intermediate in advanced material formulations.
Triallyl 1,3,5-Benzenetricarboxylate structure
17832-16-5 structure
Product Name:Triallyl 1,3,5-Benzenetricarboxylate
CAS No:17832-16-5
MF:C18H18O6
MW:330.331925868988
MDL:MFCD00008647
CID:191181
PubChem ID:87576984
Update Time:2025-10-12

Triallyl 1,3,5-Benzenetricarboxylate Chemical and Physical Properties

Names and Identifiers

    • Triallyl benzene-1,3,5-tricarboxylate
    • Triallyl 1,3,5-Benzenetricarboxylate
    • 1,3,5-Benzenetricarboxylicacid, 1,3,5-tri-2-propen-1-yl ester
    • tris(prop-2-enyl) benzene-1,3,5-tricarboxylate
    • 1,3,5-Benzenetricarboxylic Acid Triallyl Ester
    • 1,3,5-Benzenetricarboxylic acid,tri-2-propenyl ester
    • benzene-1,3,5-tricarboxylic acid triallyl ester
    • Benzol-1,3,5-tricarbonsaeure-triallylester
    • Triallyl Trimesate
    • Trimesic Acid Triallyl Ester
    • Trimesinsaeure-triallylester
    • VOSUIKFOFHZNED-UHFFFAOYSA-N
    • 1,3,5-Benzenetricarboxylic acid, tri-2-propenyl ester
    • 1,3,5-Benzenetricarboxylic acid, 1,3,5-tri-2-propen-1-yl ester
    • triallyltrimesate
    • Triallylbenzene-1,3,5-tricarboxylate
    • Tri
    • SCHEMBL254063
    • EINECS 241-791-4
    • TRIALLYL1,3,5-BENZENETRICARBOXYLATE
    • NS00025874
    • Triallyl 1,3,5-Benzenetricarboxylate, >/=98%
    • AKOS016010484
    • A881401
    • 17832-16-5
    • DTXSID3066267
    • DW4NV82JL9
    • AS-71352
    • D92471
    • T1203
    • 1,3,5-tris(prop-2-en-1-yl) benzene-1,3,5-tricarboxylate
    • UNII-DW4NV82JL9
    • FT-0765689
    • DTXCID0035669
    • MDL: MFCD00008647
    • Inchi: 1S/C18H18O6/c1-4-7-22-16(19)13-10-14(17(20)23-8-5-2)12-15(11-13)18(21)24-9-6-3/h4-6,10-12H,1-3,7-9H2
    • InChI Key: VOSUIKFOFHZNED-UHFFFAOYSA-N
    • SMILES: O(CC=C)C(C1C=C(C(=O)OCC=C)C=C(C(=O)OCC=C)C=1)=O

Computed Properties

  • Exact Mass: 330.11000
  • Monoisotopic Mass: 330.11
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 6
  • Heavy Atom Count: 24
  • Rotatable Bond Count: 12
  • Complexity: 412
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Surface Charge: 0
  • Tautomer Count: nothing
  • XLogP3: 3.4
  • Topological Polar Surface Area: 78.9

Experimental Properties

  • Color/Form: Uncertain
  • Density: 1.16
  • Melting Point: 31-34?°C(lit.)
  • Boiling Point: 212°C/2mmHg(lit.)
  • Flash Point: >230?°F
  • Refractive Index: 1.5200 (estimate)
  • PSA: 78.90000
  • LogP: 2.71500
  • Solubility: Uncertain
  • Vapor Pressure: 0.0±1.1 mmHg at 25°C

Triallyl 1,3,5-Benzenetricarboxylate Security Information

Triallyl 1,3,5-Benzenetricarboxylate Customs Data

  • HS CODE:2917399090
  • Customs Data:

    China Customs Code:

    2917399090

    Overview:

    2917399090 Other aromatic polycarboxylic acids. VAT:17.0% Tax refund rate:9.0% Regulatory conditions:nothing MFN tariff:6.5% general tariff:30.0%

    Declaration elements:

    Product Name, component content, use to, Terephthalic acid please specify4-CBAvalue, Terephthalic acid please specifyP-TLacid value, Terephthalic acid please indicate color, Terephthalic acid please indicate moisture

    Summary:

    2917399090 aromatic polycarboxylic acids, their anhydrides, halides, peroxides, peroxyacids and their derivatives.Supervision conditions:None.VAT:17.0%.Tax rebate rate:9.0%.MFN tariff:6.5%.General tariff:30.0%

Triallyl 1,3,5-Benzenetricarboxylate Pricemore >>

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Triallyl 1,3,5-Benzenetricarboxylate Related Literature

Additional information on Triallyl 1,3,5-Benzenetricarboxylate

Comprehensive Overview of Triallyl 1,3,5-Benzenetricarboxylate (CAS No. 17832-16-5): Properties, Applications, and Innovations

Triallyl 1,3,5-Benzenetricarboxylate (CAS No. 17832-16-5) is a specialized organic compound gaining attention in advanced material science and polymer chemistry. This ester derivative of benzene-1,3,5-tricarboxylic acid features three allyl groups, enabling unique crosslinking capabilities. As industries seek sustainable and high-performance materials, this compound's role in thermoset resins, photocurable coatings, and 3D printing formulations aligns with trending searches like "green polymer additives" and "high-temperature resistant materials."

The molecular structure of Triallyl 1,3,5-Benzenetricarboxylate combines a rigid aromatic core with reactive allyl functionalities, making it a versatile building block for copolymer networks. Recent studies highlight its utility in low-shrinkage dental composites—a topic frequently queried in academic databases—and flexible electronics encapsulation, addressing the demand for durable wearable tech materials. Its CAS No. 17832-16-5 is often cross-referenced with patents exploring UV-curable adhesives, reflecting industrial interest in energy-efficient processes.

Environmental considerations drive innovations involving Triallyl 1,3,5-Benzenetricarboxylate. Researchers are investigating its potential in bio-based polymer matrices, responding to queries like "biodegradable crosslinkers." Unlike traditional petrochemical alternatives, this compound's efficiency at low concentrations (1-5 wt%) reduces environmental footprint—a key point in ESG-focused material selection. Analytical techniques such as FTIR spectroscopy and DSC thermal analysis confirm its stability up to 250°C, critical for automotive and aerospace applications.

In the context of smart materials, CAS 17832-16-5 enables tunable mechanical properties when combined with nanosilica hybrids or graphene oxide. These nanocomposites answer trending searches for "self-healing coatings" and "conductive polymers." The compound's tri-functional reactivity allows precise control over crosslink density, making it ideal for shape-memory polymers—a hot topic in biomedical engineering forums.

Supply chain analytics reveal growing procurement of Triallyl 1,3,5-Benzenetricarboxylate by Asian electronic manufacturers, correlating with Google Trends data on "flexible PCB materials." Its compatibility with thiol-ene click chemistry (another frequently searched term) facilitates rapid prototyping. Regulatory databases confirm its compliance with REACH and TSCA, ensuring global market accessibility without hazardous classifications.

Future prospects for CAS No. 17832-16-5 include quantum dot encapsulation for next-gen displays and recyclable thermosets—addressing circular economy challenges. As AI-driven material discovery accelerates, this compound's structure-property relationships are being modeled via machine learning algorithms, merging computational chemistry with experimental validation.

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