| Weight | 58.08 g/mol |
|---|---|
| Formula | C3H6O |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 1 |
Propionaldehyde (123-38-6)
propanal · propionaldehyde, 2-14C-labeled · propionaldehyde, 1-14C-labeled
Score:
#280 in Physics
,
#811 in Chemistry
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- Effect of Inert Supports for Titanium Dioxide Loading on Enhancement of Photodecomposition Rate of Gaseous Propionaldehyde (The Journal of Physical Chemistry, 1995)
- Hydrogenation of carbonylic compounds: Part I: Competitive hydrogenation of propanal and acetone over noble metal catalysts (Applied Catalysis A-general, 2000)
- Preparation and use of polyethylene glycol propionaldehyde (1990)
- Microwave Spectrum of Propionaldehyde (Journal of Chemical Physics, 1964)
- The Stereochemistry of the Conversion of D and L 1,2-Propanediols to Propionaldehyde (Journal of Biological Chemistry, 1966)
- Mechanism Studies of the Fischer-Tropsch Synthesis: The Incorporation of Radioactive Ethylene, Propionaldehyde and Propanol (Journal of the American Chemical Society, 1960)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - H225: Highly Flammable liquid and vapor
Danger Flammable liquids - Category 2 - H315: Causes skin irritation
Warning Skin corrosion/irritation - Category 2 - H319: Causes serious eye irritation
Warning Serious eye damage/eye irritation - Category 2A - H332: Harmful if inhaled
Warning Acute toxicity, inhalation - Category 4 - H373: Causes damage to organs through prolonged or repeated exposure
Warning Specific target organ toxicity, repeated exposure - Category 2 - propanal
- propionaldehyde, 2-14C-labeled
- propionaldehyde, 1-14C-labeled
-
SMILESCCC=O
-
InChIKeyNBBJYMSMWIIQGU-UHFFFAOYSA-N
- Pubchem - Propionaldehyde
- Wikipedia - propionaldehyde
Propionaldehyde or propanal is the organic compound with the formula CH3CH2CHO. It is a saturated 3-carbon aldehyde and is a structural isomer of acetone. It is a colorless liquid with a slightly irritating, fruity odor.
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Trends
Alternate Names
Estimated Properties
| Boiling Point | 58.29 C | EPA T.E.S.T. |
|---|---|---|
| Density | 0.83 g/cm3 | EPA T.E.S.T. |
| Flash Point | -0.92 C | EPA T.E.S.T. |
| Water Solubility | 114404 mg/L | EPA T.E.S.T. |
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Synthesis
Similar Compounds
butyraldehyde
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(630-19-3)
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3-CHLOROPROPANAL
(19434-65-2)
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(107-22-2, 40094-65-3)
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METHACROLEIN
(4170-30-3, 78-85-3)
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2,3-butanedione
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(1191-95-3)
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(66-25-1)
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3-METHYL-2-BUTANONE
(563-80-4)
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(124-19-6)
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2-Bromomalonaldehyde
(2065-75-0)
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(111-71-7)
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(1489-69-6)
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Decanal
(112-31-2, 112-81-2)
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3,3-Dimethylbutyraldehyde
(2987-16-8)
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4-methylpentanal
(1119-16-0)
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3-Methoxypropanal
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(17157-48-1)
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(7737-17-9)
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(116-09-6)
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(1423-60-5)
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(430-51-3)
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2-Bromo-2-methylpropanal
(13206-46-7)
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3-oxobutanenitrile
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(64017-81-8)
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3-Chloropropionyl chloride
(625-36-5)
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2-Ethylbutanal
(97-96-1)
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4-Chloro-2-butanone
(6322-49-2)
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3-aminopropanamide
(4726-85-6)
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2,4-Pentanedione
(123-54-6)
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Isobutyramide
(68424-61-3, 563-83-7)
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acetate
(64-19-7, 71-50-1)
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Isobutyryl chloride
(79-30-1)
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Palladium(II) acetate
(19807-27-3, 3375-31-3)
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(557-99-3)
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(68514-31-8, 106-97-8, 68476-42-6)
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Barium acetate
(543-80-6)
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ZINC ACETATE
(557-34-6)
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(120-92-3)
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Potassium thioacetate
(10387-40-3)
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(507-09-5, 68-11-1, 10387-40-3)
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(1600-27-7, 592-63-2)
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(110-13-4)
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(6156-78-1)
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Dirhodium tetraacetate
(15956-28-2)
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Nickel(II) acetate tetrahydrate
(6018-89-9)
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(123-15-9, 73513-30-1)
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Potassium acetate
(127-08-2)
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AMMONIUM ACETATE
(631-61-8)
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Iron(II) acetate
(3094-87-9)
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5-Hexenal
(764-59-0)
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Copper(II) acetate
(142-71-2, 52503-64-7, 142-71-2, 6046-93-1)
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Cobalt(II) acetate
(71-48-7, 6147-53-1, 71-48-7, 5931-89-5)
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2-TRIDECANONE
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Pinacolone
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(4840-81-7)
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(2806-85-1)
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Propionaldehyde
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