CAS 123-38-6
:Propanal
Description:
Propanal, also known as propionaldehyde, is an aliphatic aldehyde with the molecular formula C3H6O. It is characterized by a three-carbon chain with a terminal aldehyde functional group, which imparts distinct chemical properties. Propanal is a colorless liquid at room temperature, exhibiting a pungent, fruity odor. It is soluble in water and organic solvents, making it versatile in various applications. The compound is flammable and should be handled with care, as it can form explosive mixtures with air. Propanal is primarily used in the synthesis of other chemicals, including pharmaceuticals and flavoring agents, and serves as an intermediate in organic synthesis. Its reactivity is typical of aldehydes, allowing it to participate in various chemical reactions, such as oxidation to form propanoic acid or reduction to yield propanol. Additionally, propanal can undergo condensation reactions, making it valuable in the production of larger organic molecules. Overall, propanal is an important compound in both industrial and laboratory settings due to its reactivity and utility in organic synthesis.
Formula:C3H6O
InChI:InChI=1/C3H6O/c1-2-3-4/h3H,2H2,1H3
InChI key:InChIKey=NBBJYMSMWIIQGU-UHFFFAOYSA-N
SMILES:C(C=O)C
Synonyms:- 1-Propanal
- 1-Propanone
- Ethylcarboxaldehyde
- Methylacetaldehyde
- Nsc 6493
- Propaldehyde
- Propanaldehyde
- Propional
- Propionaldehido
- Propionaldehyd
- Propionaldehyde
- Propionic aldehyde
- Propyl aldehyde
- Propylaldehyde
- Propylic aldehyde
- n-Propanal
- n-Propionaldehyde
- Propionaldhyde
- propanal
- Proprionaldehyde
- Aldehyde C(3)
- Propanal
- ethanecarbaldehyde
- ALDEHYDE C3
- femanumber2923
- Aldehyde propionique
- TRIMETHYLENE GLYCOL
- aldehydepropionique(french)
- C2H5CHO
- aldehydepropionique
- FEMA 2923
- See more synonyms
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Found 17 products.
Propionaldehyde
CAS:Formula:C3H6OPurity:>98.0%(GC)Color and Shape:Colorless clear liquidMolecular weight:58.08Propionaldehyde, 97%
CAS:<p>Propionaldehyde applications include as an intermediate, in pharmaceuticals, perfumes, plastics and polyols or polyhydric alcohols. It is also used as a precursor to trimethylolethane (CH3C(CH2OH)3) through a condensation reaction with formaldehyde, this triol is an important intermediate in the pro</p>Formula:C3H6OPurity:97%Color and Shape:Clear colorless to pale yellow, LiquidMolecular weight:58.08Propionaldehyde
CAS:Formula:CH3CH2CHOPurity:≥ 98.0%Color and Shape:Clear, colourless liquidMolecular weight:58.08Propanal
CAS:PropanalFormula:C3H6OPurity:≥95%Color and Shape: clear. almost colourless liquidMolecular weight:58.08g/molPropionaldehyde (>80%)
CAS:Controlled ProductFormula:C3H6OPurity:>80%Color and Shape:ColourlessMolecular weight:58.08Propionaldehyde
CAS:Controlled Product<p>Stability Moisture Sensitive, Volatile<br>Applications Propionaldehyde is a reagent combined with formaldehyde to produce trimethylolethane, a compound important in the production of alkyd resins. Propionaldehyde is also a strong inducer of aneuploidy in cultured Chinese hamster cells.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References Furnus, C., et al.: Mutagenesis, 5, 323 (1990); Kraft, W. & Forschirm, A.: J. Am. Oil Chem. Soc., 36, 164 (1959); Laemmle, G., et al.: Ind. Eng. Chem., 52, 33 (1960);<br></p>Formula:C3H6OColor and Shape:ColourlessMolecular weight:58.08Propionaldehyde
CAS:<p>Propionaldehyde is a simple aliphatic aldehyde that is used in the synthesis of other compounds. It can be synthesized by oxidizing propylene with an oxidation catalyst such as manganese dioxide or platinum metal under pressure. Propionaldehyde can also be formed by the direct oxidation of propanol using ferric chloride, but this reaction has been shown to produce a mixture of products. Propionaldehyde can be produced by the oxidation of acetaldehyde with hydrogen peroxide, which produces formaldehyde and acetone. In addition to its use as a chemical reagent, propionaldehyde has been used as an additive in nutrient solutions for experiments in plant physiology and microbiology.<br>The kinetic data for reactions involving propionaldehyde have been determined using methyl ethyl ketone (MEK) as the solvent and copper(II) sulfate pentahydrate as the catalyst. The redox potential for this molecule is -0.034 volts at pH 7,</p>Formula:C3H6OPurity:Min. 95%Color and Shape:Colorless Clear LiquidMolecular weight:58.08 g/molPropionaldehyde (Propanal) pure, 97%
CAS:Formula:C3H6OPurity:min. 97%Color and Shape:Clear, Yellow, LiquidMolecular weight:58.08










