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3,4-Epoxycyclohexylmethyl 3,4-epoxycyclohexanecarboxylate - 97%, high purity , CAS No.2386-87-0

    Grade & Purity:
  • ≥97%
En stock
Item Number
E103015
Articles du produit groupé
SKU Taille
Disponibilité
Prix Qté
E103015-10ml
10ml
2
19,90$US
E103015-25ml
25ml
1
39,90$US
E103015-50ml
50ml
1
69,90$US
E103015-100ml
100ml
2
109,90$US
E103015-250ml
250ml
2
229,90$US
E103015-500ml
500ml
2
359,90$US

Description générale

Synonymes Chissonox 221 monomer | 3,4-Epoxycyclohexylmethyl 3,4-epoxycyclohexane carboxylate | UT-632 | 7-Oxabicyclo[4.1.0]heptan-3-ylmethyl 7-oxabicyclo[4.1.0]heptane-3-carboxylate | ERL-4221 | 2386-87-0
Spécifications et pureté ≥97%
Température de stockage Room temperature
Expédié en Normal
Product Description

3,4-Epoxycyclohexylmethyl 3,4-epoxycyclohexanecarboxylate (EEC) is a chemical compound that belongs to the class of cycloaliphatic epoxy resins. It is commonly used as a reactive diluent or a cross-linking agent in the formulation of epoxy-based materials, such as coatings, adhesives, and composites.
It can be synthesized by the reaction of 3′-cyclohexenylmethyl 3-cyclohexenecarboxylate with peracetic acid. Its aliphatic backbone and molecular structure provide a number of useful properties such as thermal stability, weatherability, and electrical conductivity.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Organoheterocyclic compounds
Classe Oxepanes
Subclass Not available
Intermediate Tree Nodes Not available
Direct Parent Oxepanes
Alternative Parents Carboxylic acid esters  Oxacyclic compounds  Monocarboxylic acids and derivatives  Epoxides  Dialkyl ethers  Organic oxides  Hydrocarbon derivatives  Carbonyl compounds  
Molecular Framework Aliphatic heteropolycyclic compounds
Substituents Oxepane - Carboxylic acid ester - Oxacycle - Monocarboxylic acid or derivatives - Ether - Oxirane - Dialkyl ether - Carboxylic acid derivative - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aliphatic heteropolycyclic compound
Description This compound belongs to the class of organic compounds known as oxepanes. These are compounds containing an oxepane ring, which is a seven-member saturated aliphatic heterocycle with one oxygen and six carbon atoms.
External Descriptors Not available

Mécanismes d'action

Mechanism of Action Action Type target ID Target Name Target Type Target Organism Binding Site Name Références

Noms et identifiants

Pubchem Sid 488182318
Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/488182318
IUPAC Name 7-oxabicyclo[4.1.0]heptan-3-ylmethyl 7-oxabicyclo[4.1.0]heptane-3-carboxylate
INCHI InChI=1S/C14H20O4/c15-14(9-2-4-11-13(6-9)18-11)16-7-8-1-3-10-12(5-8)17-10/h8-13H,1-7H2
InChIKey YXALYBMHAYZKAP-UHFFFAOYSA-N
Smiles C1CC2C(O2)CC1COC(=O)C3CCC4C(C3)O4
Isomères SMILES C1CC2C(O2)CC1COC(=O)C3CCC4C(C3)O4
WGK Allemagne 1
RTECS RN7750000
Poids moléculaire 252.31
Reaxy-Rn 1381750
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1381750&ln=

Certificats (CoA, COO, BSE/TSE et tableau d'analyse)

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40 results found

Lot Number Certificate Type Date Article
F2104260 Certificate of Analysis Mar 03, 2025 E103015
B2505122 Certificate of Analysis Oct 16, 2024 E103015
J2429395 Certificate of Analysis Oct 16, 2024 E103015
J2429396 Certificate of Analysis Oct 16, 2024 E103015
J2429397 Certificate of Analysis Oct 16, 2024 E103015
J2429398 Certificate of Analysis Oct 16, 2024 E103015
H2428331 Certificate of Analysis Aug 02, 2024 E103015
H2426044 Certificate of Analysis Aug 02, 2024 E103015
H2426051 Certificate of Analysis Aug 02, 2024 E103015
H2426050 Certificate of Analysis Aug 02, 2024 E103015
A2408505 Certificate of Analysis Dec 27, 2023 E103015
A2408526 Certificate of Analysis Dec 27, 2023 E103015
A2408527 Certificate of Analysis Dec 27, 2023 E103015
A2408530 Certificate of Analysis Dec 27, 2023 E103015
A2408504 Certificate of Analysis Dec 27, 2023 E103015
A2408528 Certificate of Analysis Dec 27, 2023 E103015
A2408529 Certificate of Analysis Dec 27, 2023 E103015
H2312420 Certificate of Analysis Jul 21, 2023 E103015
H2312413 Certificate of Analysis Jul 21, 2023 E103015
H2312404 Certificate of Analysis Jul 21, 2023 E103015
L2315043 Certificate of Analysis Jul 21, 2023 E103015
G1506020 Certificate of Analysis Mar 09, 2023 E103015
B1925057 Certificate of Analysis Dec 12, 2022 E103015
A2306529 Certificate of Analysis Oct 22, 2022 E103015
A2306688 Certificate of Analysis Oct 22, 2022 E103015
A2306689 Certificate of Analysis Oct 22, 2022 E103015
A2306534 Certificate of Analysis Oct 22, 2022 E103015
A2306690 Certificate of Analysis Oct 22, 2022 E103015
A2306539 Certificate of Analysis Oct 22, 2022 E103015
A2306687 Certificate of Analysis Oct 22, 2022 E103015
A2306533 Certificate of Analysis Oct 22, 2022 E103015
A2306555 Certificate of Analysis Oct 22, 2022 E103015
A2306532 Certificate of Analysis Oct 22, 2022 E103015
A2306531 Certificate of Analysis Oct 22, 2022 E103015
H2205175 Certificate of Analysis Mar 23, 2022 E103015
H2205176 Certificate of Analysis Mar 23, 2022 E103015
H2205177 Certificate of Analysis Mar 23, 2022 E103015
H2205178 Certificate of Analysis Mar 23, 2022 E103015
K2119321 Certificate of Analysis Nov 25, 2021 E103015
A2214199 Certificate of Analysis Nov 25, 2021 E103015

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Propriétés chimiques et physiques

Indice de réfraction 1.498
Point d'éclair (°C) 118°C
Point de fusion (°C) -37°C
Poids moléculaire 252.310 g/mol
XLogP3 1.500
Hydrogen Bond Donor Count 0
Hydrogen Bond Acceptor Count 4
Rotatable Bond Count 4
Exact Mass 252.136 Da
Monoisotopic Mass 252.136 Da
Topological Polar Surface Area 51.400 Ų
Heavy Atom Count 18
Formal Charge 0
Complexity 356.000
Isotope Atom Count 0
Defined Atom Stereocenter Count 0
Undefined Atom Stereocenter Count 6
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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Citations of This Product

1. Zhongbo Zhu, Shumei Kang, Hua Chen, Qingping Zhao, Zhaokang Huo, Pengyu Li, Qidong Cao, Chenshuo Lu.  (2023)  Preparation and properties of CNTs-Cu hybrids/epoxy superhydrophobic and anticorrosive coatings.  JOURNAL OF INDUSTRIAL AND ENGINEERING CHEMISTRY,  119  (605).  [PMID:] [10.1016/j.jiec.2022.12.007]
2. Zhongbo Zhu, Shumei Kang, Hua Chen, Qingping Zhao, Zhaokang Huo, Pengyu Li, Jian Kang, Yansheng Yin.  (2022)  Construction of superhydrophobic alkyl siloxane-modified carbon nanotubes/epoxy coating.  DIAMOND AND RELATED MATERIALS,  129  (109351).  [PMID:] [10.1016/j.diamond.2022.109351]
3. Yue Qin, Mengdi Chen, Jinzhao Li, Yuechuan Wang.  (2022)  Synthesis and properties of cycloaliphatic diepoxides containing fluorinated linker.  JOURNAL OF APPLIED POLYMER SCIENCE,  139  (41): (e52996).  [PMID:] [10.1002/app.52996]
4. Yangyang Xu, Wenlong Tang, Hui Deng, Jianjun Zhang, Zhongquan Zhu, Changjiang Yu, Haiguang Zhu, Ke Sun, Jiazhu Li, Jacques Lalevée.  (2024)  Bisbenzothieno[b]-fused BODIPYs in panchromatic photoinitiation for free radical and cationic photopolymerization and application in 3D printing.  Polymer Chemistry,  15  (47): (4875-4887).  [PMID:] [10.1039/D4PY00926F]
5. Ying Zhang, Mingwei Wang, Ran Zhuo, Wenxu Tang, Chaolu Niu, Qiulin Chen, Weihong Yang, Sicheng Zhao.  (2025)  Study on Self-Healing Technology of Epoxy Resin for Insulator Core Rods.  JOURNAL OF APPLIED POLYMER SCIENCE,    (e56935).  [PMID:] [10.1002/app.56935]

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