Tetrahydrofurfuryl acrylate - ≥95%, contains500ppmMEHQ as stabilizer , CAS No.2399-48-6

CAS: 2399-48-6 Cat. No.: T616661 Peso molecular: 156.18 Beilstein Registry Number: 17(3/4)1104 Número EC: 219-268-7

GRADE & PURITY ≥95%, contains500ppmMEHQ as stabilizer

Synonyms

2-Propenoic acid, tetrahydrofurfuryl ester | 3-(4-Methoxyphenyl)-2-methyl-2-propenal | NSC32627 | NSC-32627 | SR 285 | CAA39948 | T2239 | (Tetrahydrofuran-2-yl)methylacrylate | AM84814 | DTXCID6024884 | Tetrahydrofurfuryl Acrylate (stabilized with MEHQ) |

Storage

Room temperature

Shipped In

Normal

Descripción general

Tetrahydrofurfuryl acrylate may be used as an acrylic matrix for silver nanoparticles/polymer nanocomposites .  It can form copolymers with butadiene. Prior to transfer printing, cellulosic and proteinic fibers are grafted with THFA.

Specifications

Sinónimos

2-Propenoic acid, tetrahydrofurfuryl ester | 3-(4-Methoxyphenyl)-2-methyl-2-propenal | NSC32627 | NSC-32627 | SR 285 | CAA39948 | T2239 | (Tetrahydrofuran-2-yl)methylacrylate | AM84814 | DTXCID6024884 | Tetrahydrofurfuryl Acrylate (stabilized with MEHQ) |

Especificaciones y pureza

≥95%, contains500ppmMEHQ as stabilizer

Condiciones de almacenamiento de almacenamiento

Room temperature

Enviado en

Normal

Pureza

≥95%

Nombres e identificadores

• Sonrisas canónicas: C=CC(=O)OCC1CCCO1
• IUPAC Name: oxolan-2-ylmethyl prop-2-enoate
• InChIKey: YNXCGLKMOXLBOD-UHFFFAOYSA-N
• INCHI: 1S/C8H12O3/c1-2-8(9)11-6-7-4-3-5-10-7/h2,7H,1,3-6H2
• Isómeros SMILES: C=CC(=O)OCC1CCCO1
• WGK Alemania: 3
• RTECS: UD3670893
• Peso molecular: 156.18
• Beilstein: 17(3/4)1104
• Reaxy-Rn: 113115

Taxonomic Classification

Taxonomy Tree

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

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Clase: Carboxylic acids and derivatives
• Subclass: Acrylic acids and derivatives
• Intermediate Tree Nodes: Not available
• Direct Parent: Acrylic acid esters
• Alternative Parents: Tetrahydrofurans Enoate esters Oxacyclic compounds Monocarboxylic acids and derivatives Dialkyl ethers Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic heteromonocyclic compounds
• Substituents: Acrylic acid ester - Tetrahydrofuran - Enoate ester - Alpha,beta-unsaturated carboxylic ester - Carboxylic acid ester - Dialkyl ether - Ether - Monocarboxylic acid or derivatives - Oxacycle - Organoheterocyclic compound - Organic oxygen compound - Organooxygen compound - Organic oxide - Hydrocarbon derivative - Carbonyl group - Aliphatic heteromonocyclic compound
• Descripción: 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: 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: Soluble in water; Soluble in Methanol,Ether
• Índice de refracción: 1.46
• Punto de inflamación (°F): 235.4 °F
• Punto de inflamación (°C): 95°C
• Punto de ebullición (°C): 87°C/9mmHg
• Peso molecular: 156.180 g/mol
• XLogP3: 1.100
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 4
• Exact Mass: 156.079 Da
• Monoisotopic Mass: 156.079 Da
• Topological Polar Surface Area: 35.500 Ų
• Heavy Atom Count: 11
• Formal Charge: 0
• Complexity: 153.000
• 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

Referencias

1. Jiajun Feng, Yuxian Xing, Chuantao Yin, Pengfei Tang, Feng Jiang.  (2023)  Wholly sustainable graft copolymers derived from cellulose, lignin, and hemicellulose for high-performance elastomers, adhesives, and UV-blocking materials.  CARBOHYDRATE POLYMERS,      [PMID:38142094] [10.1016/j.carbpol.2023.121606]

2. Yijie Liu, Yi Xue, Zifeng He, Wolin Liang, Jian Yang, Ivan S Babichuk.  (2024)  A poly(L-lactic Acid)-based flexible piezoelectric energy harvester with micro-zigzag structures.  Smart Materials and Structures,  33  (7): (075024).  [PMID:] [10.1088/1361-665X/ad4e21]

3. Deyan Du, Tatsuo Kaneko, Weifu Dong, Mingqing Chen, Dongjian Shi.  (2025)  Biomimetic Spinning of Strong and Hyperstable Eutectogel Fibers for Multifunctional Ionotronics.  ACS Applied Polymer Materials,      [PMID:] [10.1021/acsapm.4c03999]

4. Tong Luo, Ji Qi, Juan Yu, Chunpeng Wang, Fuxiang Chu, Jifu Wang.  (2024)  Lignin-Based Macromolecular Photoinitiator for Non-Migration, Self-Adhesive, and Water-Resistant Eutectogels toward Underwater Reliable Communication.  ADVANCED FUNCTIONAL MATERIALS,      [PMID:] [10.1002/adfm.202414481]

5. Jiechen Song, Yuxing Xu, Yuncheng Zhou, Rui He, Aijia Wei, Qiangqiang Tan.  (2024)  Revealing the effect of double bond-modified Li6.75La3Zr1.75Ta0.25O12 on the Li-ion conduction of composite solid electrolytes.  Materials Today Energy,      [PMID:] [10.1016/j.mtener.2024.101583]

6. Hu Rui, Zheng Anjia, Zhang Cancan, Wang Chuanxi, Zhang Jiaming, Ge Chongxiao, Li Qing, Zhang Bin, Jiang Feng.  (2025)  Preparation of cellulose-based fluorescent elastomers via RAFT polymerization and lanthanide coordination.  CELLULOSE,      [PMID:] [10.1007/s10570-025-06809-z]