Tripropylene Glycol Diacrylate (TPGDA) - ≥90%, total of isomer,stabilized with MEHQ , CAS No.42978-66-5

CAS: 42978-66-5 Cat. No.: T162230 Peso molecular: 300.35 Número EC: 256-032-2 PubChem CID: 4128060

GRADE & PURITY ≥90%, total of isomer,stabilized with MEHQ

Synonyms

TPGDA | TRPGDA | UNII-VFM08CHC4D | 1,4,7-Trimethyl-3,6-dioxaoctamethylene diacrylate | Tri(propylene glycol) diacrylate | 2-[2-(2-prop-2-enoyloxypropoxy)propoxy]propyl prop-2-enoate | tri(propyleneglycol)diacrylate

Storage

Protected from light,Room temperature,Argon charged,Desiccated,Cool

Shipped In

Normal

Descripción general

Product Introduction

Tri(propylene glycol) diacrylate (TPGDA) is a multifunctional acrylate monomer characterized by its high reactivity and ability to polymerize rapidly under UV or thermal initiation. Its structure includes multiple acrylate groups, which contribute to its crosslinking capability, enhancing the mechanical properties of the resulting polymers. The low viscosity of TPGDA facilitates easy handling and incorporation into formulations.

Application

Tri(propylene glycol) diacrylate, mixture of isomers can be used: As a cross linker to synthesize resins for flexible micromaterials via projection microstereolithography (PμSL) screening formulations to fabricate microfluidic devices for cellular biosensors. As a dopant to prepare pure organic molecules with persistent luminescence at room temperature via intramolecular electronic coupling for forensic fingerprint detection. As a precursor to prepare high mechanical resilience double network hydrogel adhesives for wound healing patches.

Specifications

Sinónimos

TPGDA | TRPGDA | UNII-VFM08CHC4D | 1, 4, 7-Trimethyl-3, 6-dioxaoctamethylene diacrylate | Tri(propylene glycol) diacrylate | 2-[2-(2-prop-2-enoyloxypropoxy)propoxy]propyl prop-2-enoate | tri(propyleneglycol)diacrylate

Especificaciones y pureza

≥90%, total of isomer, stabilized with MEHQ

Condiciones de almacenamiento de almacenamiento

Protected from light, Room temperature, Argon charged, Desiccated, Cool

Enviado en

Normal

Pureza

≥90%

Nombres e identificadores

• Pubchem Sid: 488194708
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488194708
• Sonrisas canónicas: CC(COC(C)COC(=O)C=C)OCC(C)OC(=O)C=C
• IUPAC Name: 2-[2-(2-prop-2-enoyloxypropoxy)propoxy]propyl prop-2-enoate
• InChIKey: LJRSZGKUUZPHEB-UHFFFAOYSA-N
• INCHI: 1S/C15H24O6/c1-6-14(16)20-9-12(4)18-8-11(3)19-10-13(5)21-15(17)7-2/h6-7,11-13H,1-2,8-10H2,3-5H3
• Isómeros SMILES: CC(COC(C)COC(=O)C=C)OCC(C)OC(=O)C=C
• RTECS: AT4690000
• PubChem CID: 4128060
• Peso molecular: 300.35
• Reaxy-Rn: 9213076

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • Clase Carboxylic acids and derivatives
      • Subclass Dicarboxylic acids and derivatives

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Clase: Carboxylic acids and derivatives
• Subclass: Dicarboxylic acids and derivatives
• Intermediate Tree Nodes: Not available
• Direct Parent: Dicarboxylic acids and derivatives
• Alternative Parents: Acrylic acid esters Enoate esters Dialkyl ethers Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Acrylic acid ester - Dicarboxylic acid or derivatives - Acrylic acid or derivatives - Alpha,beta-unsaturated carboxylic ester - Enoate ester - Carboxylic acid ester - Ether - Dialkyl ether - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aliphatic acyclic compound
• Descripción: This compound belongs to the class of organic compounds known as dicarboxylic acids and derivatives. These are organic compounds containing exactly two carboxylic acid groups.
• External Descriptors: Not available

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Mecanismos de acción

Propiedades químicas y físicas

• Solubilidad: Insoluble in water; Degree of Solubility in water: 0.36 g/l 25 °C; Very soluble in Alcohol,Toluene; Soluble in Acetone
• Sensibilidad: Moisture & Light sensitive.
• Índice de refracción: 1.45
• Punto de inflamación (°C): 172°C(lit.)
• Peso molecular: 300.350 g/mol
• XLogP3: 2.200
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 13
• Exact Mass: 300.157 Da
• Monoisotopic Mass: 300.157 Da
• Topological Polar Surface Area: 71.100 Ų
• Heavy Atom Count: 21
• Formal Charge: 0
• Complexity: 352.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 3
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1

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