Poly(2-ethylhexyl acrylate) solution - 25 wt% in THF,92kDa , CAS No.9003-77-4

CAS: 9003-77-4 Cat. No.: P475887 分子式: (CH₂CH[CO₂CH₂CH(C₂H₅)(CH₂)₃CH₃])n EC番号: 642-938-9

GRADE & PURITY 25 wt% in THF,92kDa

Synonyms

2-ethylhexyl-2-propenoate | NCGC00091115-01 | NCGC00256960-01 | HSDB 1121 | 2-Ethylhexylester kyseliny akrylove | acrylic acid 2-ethylhexyl ester | UNII-HR49R9S6XG | 2-Ethylhexyl Acrylate Monomer | DTXCID405297 | NCGC00091115-02 | C19420 | 2-Ethylhexylest

Storage

Protected from light,Argon charged,Room temperature

Shipped In

Normal

概要

Description

Poly(2-ethylhexyl acrylate) solution can be prepared by polymerizing 2-ethylhexyl acrylate. It may also be synthesized by solution polymerization in toluene.Poly(2-ethylhexyl acrylate) solution may be used as plasticizer for medical grade pressure sensitive adhesives.

Specifications

同義語

2-ethylhexyl-2-propenoate | NCGC00091115-01 | NCGC00256960-01 | HSDB 1121 | 2-Ethylhexylester kyseliny akrylove | acrylic acid 2-ethylhexyl ester | UNII-HR49R9S6XG | 2-Ethylhexyl Acrylate Monomer | DTXCID405297 | NCGC00091115-02 | C19420 | 2-Ethylhexylest

仕様と純度

25 wt% in THF,92kDa

保管条件

Protected from light,Argon charged,Room temperature

入荷

Normal

名前と識別子

• パブケム・シド: 528774871
• カノニカル・スマイル: CCCCC(CC)COC(=O)C=C
• IUPAC Name: 2-ethylhexyl prop-2-enoate
• InChIKey: GOXQRTZXKQZDDN-UHFFFAOYSA-N
• INCHI: 1S/C11H20O2/c1-4-7-8-10(5-2)9-13-11(12)6-3/h6,10H,3-5,7-9H2,1-2H3
• 異性体SMILES: CCCCC(CC)COC(=O)C=C
• UN番号: 1294
• Reaxy-Rn: 1765828
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1765828&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • 分類 Carboxylic acids and derivatives
      • Subclass Acrylic acids and derivatives

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• 分類: Carboxylic acids and derivatives
• Subclass: Acrylic acids and derivatives
• Intermediate Tree Nodes: Not available
• Direct Parent: Acrylic acid esters
• Alternative Parents: Enoate esters Monocarboxylic acids and derivatives Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Acrylic acid ester - Alpha,beta-unsaturated carboxylic ester - Enoate ester - Carboxylic acid ester - Monocarboxylic acid or derivatives - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aliphatic acyclic compound
• 説明: This compound belongs to the class of organic compounds known as acrylic acid esters. These are organic compounds containing and ester acrylic acid (CH2=CHC(=O)OH).
• External Descriptors: enoate ester

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

関連ターゲット（人間）

TSHR Tclin Thyroid stimulating hormone receptor (29986 Activities)

Discover Target: TSHR

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

作用メカニズム

化学的性質と物理的性質

• 感度: light sensitive
• 引火点（°F）: 39.2 °F - closed cup
• 引火点（°C）: 4.0 °C - closed cup
• 融点（°C）: Tg−55℃
• 分子量: 184.270 g/mol
• XLogP3: 3.800
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 8
• Exact Mass: 184.146 Da
• Monoisotopic Mass: 184.146 Da
• Topological Polar Surface Area: 26.300 Ų
• Heavy Atom Count: 13
• Formal Charge: 0
• Complexity: 152.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 1
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1

参考文献

1. Xinlei Wu, Jun Yao, Yingjie Guo, Sijia Zheng, Zhihai Cao.  (2023)  Manipulation of surface properties and long-term antibacterial performance of composite films via alkyl side chain engineering.  PROGRESS IN ORGANIC COATINGS,      [PMID:] [10.1016/j.porgcoat.2023.107852]