≥98%(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 1 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Stereochemistry of kinetic Michael addition of the Z and E lithium enolates of tert-butyl propionate has been investigated
| Pubchem Sid | 504755951 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/504755951 |
| Sonrisas canónicas | CCC(=O)OC(C)(C)C |
| IUPAC Name | tert-butyl propanoate |
| InChIKey | JAELLLITIZHOGQ-UHFFFAOYSA-N |
| INCHI | 1S/C7H14O2/c1-5-6(8)9-7(2,3)4/h5H2,1-4H3 |
| Isómeros SMILES | CCC(=O)OC(C)(C)C |
| WGK Alemania | 3 |
| PubChem CID | 88561 |
| Número ONU | 1914 |
| Grupo de embalaje | III |
| Peso molecular | 130.19 |
| Beilstein | 1747860 |
| Reaxy-Rn | 1747857 |
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 acids and derivatives |
| Clase | Carboxylic acids and derivatives |
| Subclass | Carboxylic acid derivatives |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Carboxylic acid esters |
| Alternative Parents | Monocarboxylic acids and derivatives Organic oxides Hydrocarbon derivatives Carbonyl compounds |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Carboxylic acid ester - Monocarboxylic acid or derivatives - 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 carboxylic acid esters. These are carboxylic acid derivatives in which the carbon atom from the carbonyl group is attached to an alkyl or an aryl moiety through an oxygen atom (forming an ester group). |
| External Descriptors | Not available |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Fecha | Articulo |
|---|---|---|---|
 H2422187 | Certificate of Analysis | Jun 18, 2024 | T162406 |
| H2422526 | Certificate of Analysis | Jun 18, 2024 | T162406 |
| H2518667 | Certificate of Analysis | Jun 18, 2024 | T162406 |
| I2301126 | Certificate of Analysis | Sep 06, 2023 | T162406 |
| I2301127 | Certificate of Analysis | Sep 06, 2023 | T162406 |
| I2301128 | Certificate of Analysis | Sep 06, 2023 | T162406 |
| I2301727 | Certificate of Analysis | Sep 06, 2023 | T162406 |
| I2504052 | Certificate of Analysis | Sep 06, 2023 | T162406 |
| C1812185 | Certificate of Analysis | Jan 27, 2022 | T162406 |
| F2316079 | Certificate of Analysis | Jan 27, 2022 | T162406 |
| Índice de refracción | 1.39 |
|---|---|
| Punto de inflamación (°F) | 69.8 °F |
| Punto de inflamación (°C) | 21 °C |
| Punto de ebullición (°C) | 119 °C |
| Peso molecular | 130.180 g/mol |
| XLogP3 | 1.600 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 3 |
| Exact Mass | 130.099 Da |
| Monoisotopic Mass | 130.099 Da |
| Topological Polar Surface Area | 26.300 Ų |
| Heavy Atom Count | 9 |
| Formal Charge | 0 |
| Complexity | 100.000 |
| 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 |
| 1. Wenna Tang, Letao Guo, Lixia Yang, Liewei Qiu, Hongchen Liu, Mei Yang. (2026) Enhanced utilization of ester enolates in slow-kinetic α-functionalization of esters: Insights into enolate consumption and preservation strategies. CHEMICAL ENGINEERING SCIENCE, [PMID:] [10.1016/j.ces.2026.123675] |
