Trimethylolpropane allyl ether(TMPME) - ≥95% , CAS No.682-11-1

CAS: 682-11-1 Cat. No.: T487225 Formule: C₉H₁₈O₃ Poids moléculaire: 174.24 Numéro CE: 211-662-7 PubChem CID: 12683

GRADE & PURITY ≥95%

Synonyms

2-ethyl-2-(prop-2-enoxymethyl)propane-1,3-diol | 1,1,1-Trimethylolpropane monoallyl ether | 2-(Allyloxymethyl)-2-ethyl-1,3-propanediol

Storage

Protected from light,Room temperature

Shipped In

Normal

Vue d’ensemble

Trimethylolpropane diallylether.The molecular structure contains two hydroxyl groups and one double bond, primarily used for silicone modification, polyurethane-modified water-soluble resins, epoxy resins, cross-linking agents in the main chains of unsaturated polyesters, and automotive coatings.

Specifications

Synonymes

2-ethyl-2-(prop-2-enoxymethyl)propane-1,3-diol | 1,1,1-Trimethylolpropane monoallyl ether | 2-(Allyloxymethyl)-2-ethyl-1,3-propanediol

Spécifications et pureté

≥95%

Conditions de stockage de stockage

Protected from light,Room temperature

Expédié en

Normal

Pureté

≥95%

Noms et identifiants

• Pubchem Sid: 504752382
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504752382
• Sourires canoniques: CCC(CO)(CO)COCC=C
• IUPAC Name: 2-ethyl-2-(prop-2-enoxymethyl)propane-1,3-diol
• InChIKey: LZDXRPVSAKWYDH-UHFFFAOYSA-N
• INCHI: 1S/C9H18O3/c1-3-5-12-8-9(4-2,6-10)7-11/h3,10-11H,1,4-8H2,2H3
• Isomères SMILES: CCC(CO)(CO)COCC=C
• PubChem CID: 12683
• Poids moléculaire: 174.24

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic oxygen compounds
    • Classe Organooxygen compounds
      • Subclass Ethers

• Kingdom: Organic compounds
• Superclass: Organic oxygen compounds
• Classe: Organooxygen compounds
• Subclass: Ethers
• Intermediate Tree Nodes: Not available
• Direct Parent: Dialkyl ethers
• Alternative Parents: Primary alcohols Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Dialkyl ether - Hydrocarbon derivative - Primary alcohol - Alcohol - Aliphatic acyclic compound
• Description: This compound belongs to the class of organic compounds known as dialkyl ethers. These are organic compounds containing the dialkyl ether functional group, with the formula ROR', where R and R' are alkyl 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

Propriétés chimiques et physiques

• Sensibilité: Light sensitive
• Indice de réfraction: n20/D 1.467 (lit.)
• Point d'éclair (°F): 235.4 °F - closed cup
• Point d'éclair (°C): 113 °C - closed cup
• Point d'ébullition (°C): 160℃/33mmHg (lit.)
• Poids moléculaire: 174.240 g/mol
• XLogP3: 0.400
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 7
• Exact Mass: 174.126 Da
• Monoisotopic Mass: 174.126 Da
• Topological Polar Surface Area: 49.700 Ų
• Heavy Atom Count: 12
• Formal Charge: 0
• Complexity: 119.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1

Références

1. Haodi Min, Nan Zheng, Zengju Fan, Youwei Jiang, Xing Cheng.  (2018)  UV-curable nanoimprint resist with liquid volume-expanding monomers.  MICROELECTRONIC ENGINEERING,      [PMID:] [10.1016/j.mee.2018.10.011]