average Mₙ ~870 for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Room temperature Ships Check lot-specific COA for exact specifications.
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Description
For high temperature adhesives, coatings, electrical and laminating products.Poly[(o-cresyl glycidyl ether)-co-formaldehyde] is anO-cresol formaldehyde based epoxy resin that can be cured using polyethylene amine. It can be used in the formation of abrasion resistant coatings for potential applications in sensors, anti-reflective, electrochromic and antimicrobial coatings. It can also be used in the formation of polyaniline based adhesive for organic electronics.
| Sonrisas canónicas | CC1=CC=CC=C1O.C=O.C1C(O1)CCl |
|---|---|
| IUPAC Name | 2-(chloromethyl)oxirane;formaldehyde;2-methylphenol |
| InChIKey | XRYDVSRMOIMZGM-UHFFFAOYSA-N |
| INCHI | 1S/C7H8O.C3H5ClO.CH2O/c1-6-4-2-3-5-7(6)8;4-1-3-2-5-3;1-2/h2-5,8H,1H3;3H,1-2H2;1H2 |
| Isómeros SMILES | CC1=CC=CC=C1O.C=O.C1C(O1)CCl |
| PubChem CID | 94405 |
| Peso molecular | 230.69 |
Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS →Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA →Full quality attributes and acceptance criteria for this grade.
View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Benzenoids |
| Clase | Phenols |
| Subclass | Cresols |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Ortho cresols |
| Alternative Parents | Toluenes 1-hydroxy-4-unsubstituted benzenoids 1-hydroxy-2-unsubstituted benzenoids Oxacyclic compounds Epoxides Dialkyl ethers Organochlorides Organic oxides Hydrocarbon derivatives Carbonyl compounds Alkyl chlorides |
| Molecular Framework | Not available |
| Substituents | O-cresol - 1-hydroxy-4-unsubstituted benzenoid - 1-hydroxy-2-unsubstituted benzenoid - Toluene - Monocyclic benzene moiety - Oxacycle - Organoheterocyclic compound - Ether - Oxirane - Dialkyl ether - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organochloride - Organohalogen compound - Carbonyl group - Alkyl halide - Alkyl chloride - Aromatic heteromonocyclic compound |
| Descripción | This compound belongs to the class of organic compounds known as ortho cresols. These are organic compounds containing an ortho-cresol moiety, which consists of a benzene bearing one hydroxyl group at ring positions 1 and 2, respectively. |
| External Descriptors | Not available |
| Punto de inflamación (°F) | 235.4 °F - closed cup |
|---|---|
| Punto de inflamación (°C) | 113 °C - closed cup |
| Punto de fusión (°C) | 70-75℃ (lit.)70-75℃ |
| Peso molecular | 230.690 g/mol |
| XLogP3 | |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 3 |
| Rotatable Bond Count | 1 |
| Exact Mass | 230.071 Da |
| Monoisotopic Mass | 230.071 Da |
| Topological Polar Surface Area | 49.800 Ų |
| Heavy Atom Count | 15 |
| Formal Charge | 0 |
| Complexity | 111.000 |
| 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 | 3 |
![Poly[(o-cresyl glycidyl ether)-co-formaldehyde] - average Mₙ ~870 CAS No(29690-82-2) by Aladdin Scientific](https://www.aladdinsci.com/media/catalog/product/cache/207e23213cf636ccdef205098cf3c8a3/P/4/P477990.png)