≥99% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Store at 2-8°C,Argon charged Ships Wet ice 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 8 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Treatment of 4-formylmorpholine with sulphur tetrafluoride in the presence of potassium fluoride gives 4-(trifluoromethyl)morpholine in excellent yields. 4-Formylmorpholine reacts with series of 2-alkyl-2-cyclohexen-1-ones in the presence of POCl3 to give the corresponding 3-alkyl-2-chloro-5,6-dihydrobenzaldehydes and allylic alcohols (by-product).
4-Formylmorpholine has been used in the preparation of: ? adenine hydrochloride labelled with 14C ? terphenyl dialdehyde
| Pubchem Sid | 504752979 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/504752979 |
| Sonrisas canónicas | C1COCCN1C=O |
| IUPAC Name | morpholine-4-carbaldehyde |
| InChIKey | LCEDQNDDFOCWGG-UHFFFAOYSA-N |
| INCHI | 1S/C5H9NO2/c7-5-6-1-3-8-4-2-6/h5H,1-4H2 |
| Isómeros SMILES | C1COCCN1C=O |
| WGK Alemania | 3 |
| RTECS | QD9694000 |
| Peso molecular | 115.13 |
| Beilstein | 110293 |
| Reaxy-Rn | 110293 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=110293&ln= |
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 | Organoheterocyclic compounds |
| Clase | Oxazinanes |
| Subclass | Morpholines |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Morpholines |
| Alternative Parents | Tertiary carboxylic acid amides Oxacyclic compounds Dialkyl ethers Azacyclic compounds Organopnictogen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds |
| Molecular Framework | Aliphatic heteromonocyclic compounds |
| Substituents | Morpholine - Tertiary carboxylic acid amide - Carboxamide group - Carboxylic acid derivative - Dialkyl ether - Ether - Oxacycle - Azacycle - Carbonyl group - Organooxygen compound - Organonitrogen compound - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organic oxygen compound - Organic nitrogen compound - Aliphatic heteromonocyclic compound |
| Descripción | This compound belongs to the class of organic compounds known as morpholines. These are organic compounds containing a morpholine moiety, which consists of a six-member aliphatic saturated ring with the formula C4H9NO, where the oxygen and nitrogen atoms lie at positions 1 and 4, respectively. |
| External Descriptors | morpholines |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Fecha | Articulo |
|---|---|---|---|
 F2616070 | Certificate of Analysis | Jun 30, 2026 | F111002 |
| F2617070 | Certificate of Analysis | Jun 27, 2026 | F111002 |
| G2209216 | Certificate of Analysis | Apr 07, 2026 | F111002 |
| G2209228 | Certificate of Analysis | Apr 07, 2026 | F111002 |
| G2209232 | Certificate of Analysis | Apr 07, 2026 | F111002 |
| G2209254 | Certificate of Analysis | Apr 07, 2026 | F111002 |
| K2117949 | Certificate of Analysis | Sep 04, 2025 | F111002 |
| J1826096 | Certificate of Analysis | Aug 15, 2022 | F111002 |
| A2426059 | Certificate of Analysis | Jun 20, 2022 | F111002 |
| G2209227 | Certificate of Analysis | Jun 20, 2022 | F111002 |
| J2429183 | Certificate of Analysis | Jun 20, 2022 | F111002 |
| J2511118 | Certificate of Analysis | Jun 20, 2022 | F111002 |
| K2505125 | Certificate of Analysis | Jun 20, 2022 | F111002 |
| Solubilidad | Miscible with water. |
|---|---|
| Sensibilidad | Moisture & heat sensitive |
| Índice de refracción | 1.485 |
| Punto de inflamación (°F) | 257 °F |
| Punto de inflamación (°C) | 125 °C |
| Punto de ebullición (°C) | 236-237°C |
| Punto de fusión (°C) | 22-24 °C |
| Peso molecular | 115.130 g/mol |
| XLogP3 | -0.600 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 0 |
| Exact Mass | 115.063 Da |
| Monoisotopic Mass | 115.063 Da |
| Topological Polar Surface Area | 29.500 Ų |
| Heavy Atom Count | 8 |
| Formal Charge | 0 |
| Complexity | 78.500 |
| 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 |
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| 6. Yuxin Zhou, Tianhuan Huang, Shaohua Zhong, Xiaoqing Li, Yiwen Chen, Kunyao Su, Weihuang Yang, Jiangrong Lu, Jian Zhang. (2025) PVDF-HFP gel polymer electrolytes with a uniform porous network for lithium metal batteries. JOURNAL OF POWER SOURCES, [PMID:] [10.1016/j.jpowsour.2025.238207] |
| 7. Jun Li, Wanting Yu, Jinsen Gao. (2025) Separation of polycyclic aromatic hydrocarbons by solvent screening assisted extractive distillation from FCC diesel. CHINESE JOURNAL OF CHEMICAL ENGINEERING, [PMID:] [10.1016/j.cjche.2025.09.001] |
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