2-Carboxyethyl acrylate - ≥90%, contains 900-1100 ppm MEHQ as inhibitor , CAS No.24615-84-7

CAS: 24615-84-7 Cat. No.: C303186 Peso molecular: 144.13 Número EC: 246-359-9

GRADE & PURITY ≥90%, contains 900-1100 ppm MEHQ as inhibitor

Synonyms

3-prop-2-enoyloxypropanoic acid | beta-Carboxyethyl acrylate | Hydracrylic acid acrylate | 2-Carboxyethyl 2-propenoate | 3-(acryloyloxy)propanoic acid | 2-carboxyethylacrylate

Storage

Store at 2-8°C,Desiccated

Shipped In

Wet ice

Descripción general

Can be polymerized in solution or emulsion to produce acrylic, vinyl-acrylic, or styrenic-acrylic polymers with greater flexibility due to lower glass transition of itshomopolymer (<30C) and improved adhesion.More reactive in its salt form than acylic acid, allowing high levels of incorporation over awide pH range.

Specifications

Sinónimos

3-prop-2-enoyloxypropanoic acid | beta-Carboxyethyl acrylate | Hydracrylic acid acrylate | 2-Carboxyethyl 2-propenoate | 3-(acryloyloxy)propanoic acid | 2-carboxyethylacrylate

Especificaciones y pureza

≥90%, contains 900-1100 ppm MEHQ as inhibitor

Condiciones de almacenamiento de almacenamiento

Store at 2-8°C, Desiccated

Enviado en

Wet ice

Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.

Pureza

≥90%

Nombres e identificadores

• Pubchem Sid: 504756033
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504756033
• Sonrisas canónicas: C=CC(=O)OCCC(=O)O
• IUPAC Name: 3-prop-2-enoyloxypropanoic acid
• InChIKey: CYUZOYPRAQASLN-UHFFFAOYSA-N
• INCHI: 1S/C6H8O4/c1-2-6(9)10-4-3-5(7)8/h2H,1,3-4H2,(H,7,8)
• Isómeros SMILES: C=CC(=O)OCCC(=O)O
• Peso molecular: 144.13
• Reaxy-Rn: 1766057
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1766057&ln=

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 Carboxylic acids 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 - Carboxylic acid - 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

Propiedades químicas y físicas

• Solubilidad: H2O: soluble
• Índice de refracción: n20/D 1.457(lit.)
• Punto de ebullición (°C): 103 °C19 mm Hg(lit.)
• Peso molecular: 144.120 g/mol
• XLogP3: 0.200
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 5
• Exact Mass: 144.042 Da
• Monoisotopic Mass: 144.042 Da
• Topological Polar Surface Area: 63.600 Ų
• Heavy Atom Count: 10
• Formal Charge: 0
• Complexity: 150.000
• 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

Referencias

1. Zhijun Liu, Guoming Yuan, Hui Yang, Kunxin Wang, Yanghan Tao, Kun Wu, Jun Shi, Li Yang.  (2025)  High-performance PSA with dual-network structure for enhanced cohesion.  COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS,      [PMID:] [10.1016/j.colsurfa.2025.136271]

2. Wenhui Wang, Xinyu Zeng, Zhiliang Gao, Linqiang Mei, Chang Pan, Jie Li, Yuguo Chen.  (2025)  A polymer-based “immunogenic cell death” amplifier promotes systemic breast cancer inhibition through combined mitochondrial oxidative stress and calcium overload.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2025.165725]

3. Yong Liu, Jiaming Guo, Zongwei Guo, Lei Shang, Yuhui Ao.  (2025)  Study on the Thermal Stabilization Behavior of Poly(Acrylonitrile-co-2-Carboxyethyl Acrylate) Copolymer as Potential Precursor of Carbon Fiber.  POLYMERS FOR ADVANCED TECHNOLOGIES,  36  (9): (e70304).  [PMID:] [10.1002/pat.70304]

4. Xue Longlong, Xiong Shisheng.  (2024)  Flexible metal foil/polymer sandwich composites for electromagnetic interference shielding with anti-wind–sand environment tolerance.  JOURNAL OF MATERIALS SCIENCE-MATERIALS IN ELECTRONICS,  35  (25): (1-13).  [PMID:] [10.1007/s10854-024-13427-1]

5. Qihang Wang, Jiqiong Liu, Huichao Lu, Shuo Liu, Liangyu Wang, Chenran Hao, Jing Han, Jun Yang, Yanna NuLi, Jiulin Wang.  (2025)  A Rigid-flexible binder for sulfurized polyacrylonitrile cathodes for rechargeable lithium batteries.  Journal of Materials Chemistry A,      [PMID:] [10.1039/D5TA01612F]

6. Zhijun Liu, Fei Cheng, Guoming Yuan, Yanhan Tao, Yihao Yang, Bo Yang, Kun Wu, Jun Shi, Guangwen Che.  (2026)  Low-voltage-triggered rapid electrical detachment of pressure-sensitive adhesives via ion transport channels.  Journal of Materials Chemistry A,      [PMID:] [10.1039/D5TA08214E]