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Propionaldehyde

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CAS:123-38-6
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  • Propionaldehyde
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  • CAS:123-38-6
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Propionaldehyde Basic information
Product Name:Propionaldehyde
Synonyms:aldehydepropionique;aldehydepropionique(french);ethanecarbaldehyde;Ethylcarboxaldehyde;femanumber2923;NCI-C61029;n-Propylal;Aldehyde C-3, Propanal
CAS:123-38-6
MF:C3H6O
MW:58.08
EINECS:204-623-0
Product Categories:
Mol File:123-38-6.mol
Propionaldehyde Structure
Propionaldehyde Chemical Properties
Melting point -81 °C (lit.)
Boiling point 46-50 °C (lit.)
density 0.805 g/mL at 25 °C (lit.)
vapor density 2 (vs air)
vapor pressure 18.77 psi ( 55 °C)
refractive index n20/D 1.362(lit.)
FEMA 2923 | PROPIONALDEHYDE
Fp −16 °F
storage temp. Store at <= 20°C.
solubility soluble in chloroform; miscible with alcohol and ether
form Liquid
Specific Gravity0.815 (20/4℃)
color White
Odorat 0.10 % in propylene glycol. earthy alcohol wine whiskey cocoa nutty
Odor Typeethereal
explosive limit2.3-21%(V)
Odor Threshold0.001ppm
Water Solubility 540 g/L (20 ºC)
Sensitive Air Sensitive
JECFA Number83
Merck 14,7823
BRN 506010
Dielectric constant18.9(17℃)
Exposure limitsACGIH: TWA 20 ppm
Stability:Stable. Highly flammable. Incompatible with oxidizing agents, strong acids, strong bases.
InChIKeyNBBJYMSMWIIQGU-UHFFFAOYSA-N
LogP0.59 at 25℃
CAS DataBase Reference123-38-6(CAS DataBase Reference)
NIST Chemistry ReferencePropanal(123-38-6)
EPA Substance Registry SystemPropionaldehyde (123-38-6)
Safety Information
Hazard Codes F,Xi,Xn
Risk Statements 11-36/37/38-R36/37/38-R11-41-37/38-20/22
Safety Statements 9-16-29-S9-S29-S16
RIDADR UN 1275 3/PG 2
WGK Germany 1
RTECS UE0350000
Autoignition Temperature404 °F
TSCA Yes
HazardClass 3
PackingGroup II
HS Code 29121900
Hazardous Substances Data123-38-6(Hazardous Substances Data)
ToxicityLD50 orally in rats: 1.4 g/kg; LC for rats in air: 8000 ppm (Smyth)
MSDS Information
ProviderLanguage
ACROS English
SigmaAldrich English
ALFA English
Propionaldehyde Usage And Synthesis
DescriptionPropionaldehyde is a volatile liquid substance which consists of one carbonyl group and its characteristic functional group. The main functional group is an aldehyde which classifies propionaldehyde in the carbonyls. The main trunk of this substance is a short aliphatic chain. The carbonyl group determines, to a large extent, its chemical properties and most importantly its nucleophilic property. Propionaldehyde is readily oxidized if in contact to oxygen and should therefore be stored under inert gases.
Chemical PropertiesPropionaldehyde has a characteristic sharp and pungent odor similar to acetaldehyde.It undergoes reactions typical for the low molecular weight aldehydes, which, because of the terminal carbonyl group, are very reactive. Contamination or the exposure to elevated temperatures may induce a hazardous polymerization.
Propionaldehyde
Propionaldehyde is a colorless, flammable liquid with a suffocating fruity odor. It is used as Intermediate for the chemical industry, for example for the manufacture of pharmaceuticals, pesticides, perfumes and plastics.
OccurrenceReported found in apple aroma and in the essential oils of camphor, Rosa centifolia, clary sage, Pinus excelsa and Pinus silverstris. Also reported found in over 100 natural products including apple, banana, sweet cherry, sour cherry, black currant grapes, melon, pineapple, strawberry, cabbage, carrot, celery, cucumber, garlic, onion, leek, potato, peas, rutabaga, tomato, Scotch spearmint oil, vinegar, bread and bread preferment, blue cheeses, cheddar cheese, Swiss cheese, butter, milk, cream, boiled egg, caviar, fatty fish, cooked turkey, beef, pork and chicken, beer, rum, cognac, whiskies, grape wines, coffee, cocoa, tea, roasted filberts and peanuts, peanut oil, potato chips, pecans, oats, honey, soybeans, Arctic bramble, beans, Bantu beer, plum brandy, cauliflower, Brussels sprouts, rice, prickly pear, peated malt, clary sage, truffle, krill, oysters, loganberry, Chinese quince and maté.
UsesPropionaldehyde is produced by the oxo reaction of ethylene with carbon monoxide and hydrogen. n-Propyl alcohol is produced by hydrogenation of propionaldehyde, and propionic acid is made by oxidation of propionaldehyde.
n-Propyl alcohol is used as solvent in printing inks and as an intermediate in the preparation of agricultural chemicals. Propionic acid is used as a grain preservative as, for example, in preventing spoilage of wet corn used as animal feed. The use of propionic acid as a grain preservative is an alterna tive to drying by heating, which consumes fuel, and is considered mostly when fuel is expensive.
UsesManufacture of propionic acid, polyvinyl, and other plastics; synthesis of rubber chemicals; disin- fectant; preservative.
UsesPropionaldehyde is used in the productionof propionic acid, propionic anhydride, andmany other compounds. It is formed in theoxidative deterioration of corn products, suchas corn chips. It occurs in automobile exhaustgases.
PreparationBy oxidation of propyl alcohol, or by dry distillation of barium propionate with calcium formate.
PreparationPropionaldehyde is prepared in the usual way by the oxidation of n-propyl alcohol. It can also be prepared by dehydrogenating the alcohol by passing the vapors over a heated copper or brass catalyst. This avoids the danger of further oxidation to propionic acid.
The reactions of propionaldehyde are practically like those of acetaldehyde. It must be remembered that only the two alpha hydrogen atoms are active in replacement and condensation reactions.
DefinitionChEBI: An aldehyde that consists of ethane bearing a formyl substituent. The parent of the class of propanals.
General DescriptionA clear colorless liquid with an overpowering fruity-like odor. Less dense than water. Flash point 15°F. Vapors are heavier than air.
Air & Water ReactionsHighly flammable. Soluble in water.
Reactivity ProfilePropionaldehyde may form explosive peroxides. Reacts vigorously with oxidizing agents. Explosive in the form of vapor when exposed to heat or flame [Lewis]. Incompatible with strong bases and strong reducing agents. Vigorous polymerization reaction with methyl methacrylate. Polymerization may also occur in the presence of acids or caustics .
HazardFlammable, dangerous fire risk, explosive limits in air 3.0–16%. Upper respiratory tract irri- tant.
Health HazardPropionaldehyde is a mild irritant to humanskin and eyes. The irritation effect from40 mg was severe in rabbits’ eyes. The toxicityof this compound observed in test animalswas low. Subcutaneous administration in ratsexhibited the symptoms of general anestheticeffect, convulsion, and seizure. Inhalationtoxicity was determined to be low. A concentrationof 8000 ppm (19,000 mg/m3) inair was lethal to rats.
LD50 value, oral (rats): 1400 mg/kg
LD50 subcutaneous (rats): 820 mg/kg.
Fire HazardBehavior in Fire: Vapor is heavier than air and may travel considerable distance to a source of ignition and flash back.
Flammability and ExplosibilityFlammable
Biochem/physiol ActionsTaste at 5-10 ppm
Safety ProfileModerately toxic by skin contact, ingestion, and subcutaneous routes. Mddly toxic by inhalation. A skin and severe eye irritant. Flammable liquid. Dangerous fire hazard when exposed to heat or flame; reacts vigorously with oxidizers. Explosive in the form of vapor when exposed to heat or flame. Vigorous polymerization reaction with methyl methacrylate. To fight fire, use alcohol foam, CO2, dry chemical. When heated to decomposition it emits acrid smoke and irritating fumes. See also ALDEHYDES.
Potential ExposureUsed as a synthetic flavoring; as a disinfectant and preservative; to make propionic acid; in plastic and rubber manufacturing; to make alkyl resins and plasticizers.
CarcinogenicityIn a mutagenic test in V79 cells, Eder et al. observed that propionaldehyde is not mutagenic at 1 mM, but is toxic at 2mM. Similar to acrolein, Eder et al. suggested that the mutagenicity of this compound is mediated by its bifunctionality, whereas its cytotoxicity is mediated by the aldehyde function.
ShippingUN1275 Propionaldehyde, Hazard Class: 3; Labels: 3-Flammable liquid.
Propionaldehyde is readily oxidized if in contact to oxygen and should therefore be stored under inert gases.
Purification Methodsthe aldehyde with CaSO4 or CaCl2, and fractionally distil it under nitrogen or in the presence of a trace of hydroquinone (to retard oxidation). Blacet and Pitts [J Am Chem Soc 74 3382 1952] repeatedly distilled the middle fraction in a vacuum until it no longer gave a solid polymer when cooled to -80o. It is stored with CaSO4. [Beilstein 1 IV 3165.]
IncompatibilitiesIncompatible with strong acids; amines. Incompatible with oxidizers (chlorates, nitrates, peroxides, permanganates, perchlorates, chlorine, bromine, fluorine, etc.); contact may cause fires or explosions. Keep away from alkaline materials, strong bases, strong acids, oxoa- cids, epoxides. Strong caustics; reducing agents can cause explosive polymerization. Can self-ignite if finely dispersed on porous or combustible material, such as fabric. Heat or UV light can cause decomposition. Aldehydes are fre- quently involved in self-condensation or polymerization reactions. These reactions are exothermic; they are often catalyzed by acid. Aldehydes are readily oxidized to give carboxylic acids. Flammable and/or toxic gases are gener- ated by the combination of aldehydes with azo, diazo com- pounds, dithiocarbamates, nitrides, and strong reducing agents. Aldehydes can react with air to give first peroxo acids, and ultimately carboxylic acids. These autoxidation reactions are activated by light, catalyzed by salts of transition metals, and are autocatalytic (catalyzed by the products of the reaction). The addition of stabilizers (anti- oxidants) to shipments of aldehydes retards autoxidation
Waste DisposalPropionaldehyde is destroyed by burning in achemical incinerator equipped with an afterburnerand scrubber. Permanganate oxidationis a suitable laboratory method of destruction.
Tag:Propionaldehyde(123-38-6) Related Product Information
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