Determine the necessary mass, volume, or concentration for preparing a solution.
≥95%(GC) for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Room temperature Ships Normal 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.
1,4-Dioxaspiro[4.5]decan-2-one has been used in the synthesis of L-callipeltose, the deoxyamino sugar of L-callipeltoside A.
| Pubchem Sid | 488190218 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/488190218 |
| Sonrisas canónicas | C1CCC2(CC1)OCC(=O)O2 |
| IUPAC Name | 1,4-dioxaspiro[4.5]decan-3-one |
| InChIKey | HBGAMCTZOLJGAS-UHFFFAOYSA-N |
| INCHI | 1S/C8H12O3/c9-7-6-10-8(11-7)4-2-1-3-5-8/h1-6H2 |
| Isómeros SMILES | C1CCC2(CC1)OCC(=O)O2 |
| WGK Alemania | 3 |
| PubChem CID | 544223 |
| Peso molecular | 156.18 |
| Reaxy-Rn | 1239446 |
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 | Organic oxygen compounds |
| Clase | Organooxygen compounds |
| Subclass | Ethers |
| Intermediate Tree Nodes | Acetals |
| Direct Parent | Ketals |
| Alternative Parents | 1,3-dioxolanes Lactones Carboxylic acid esters Oxacyclic compounds Monocarboxylic acids and derivatives Organic oxides Hydrocarbon derivatives Carbonyl compounds |
| Molecular Framework | Aliphatic heteropolycyclic compounds |
| Substituents | Ketal - Meta-dioxolane - Lactone - Carboxylic acid ester - Oxacycle - Organoheterocyclic compound - Monocarboxylic acid or derivatives - Carboxylic acid derivative - Organic oxide - Hydrocarbon derivative - Carbonyl group - Aliphatic heteropolycyclic compound |
| Descripción | This compound belongs to the class of organic compounds known as ketals. These are acetals derived from ketones by replacement of the oxo group by two hydrocarbyloxy groups R2C(OR)2 ( R not Hydrogen ). This term, once abandoned, has been reinstated as a subclass of acetals. |
| External Descriptors | Not available |
| Punto de inflamación (°F) | 221 °F |
|---|---|
| Punto de inflamación (°C) | 105 °C |
| Punto de ebullición (°C) | 70 °C/0.5 mmHg |
| Punto de fusión (°C) | 32-35°C |
| Peso molecular | 156.180 g/mol |
| XLogP3 | 1.500 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 3 |
| Rotatable Bond Count | 0 |
| 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 | 170.000 |
| 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 |