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Propionaldehyde

Propionaldehyde

CAS: 123-38-6

Molecular Formula: C3H6O

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Propionaldehyde - Names and Identifiers

Name Propionaldehyde
Synonyms C2H5CHO
propanal
NCI-C61029
propaldehyde
Aldehyde C(3)
femanumber2923
Propionaldhyde
Propyl aldehyde
Propionaldehyde
Proprionaldehyde
propylic aldehyde
n-Propionaldehyde
Methylacetaldehyde
ethanecarbaldehyde
Propionic aldehyde
aldehydepropionique
Ethylcarboxaldehyde
aldehydepropionique(french)
CAS 123-38-6
EINECS 204-623-0
InChI InChI=1/C3H6O/c1-2-3-4/h3H,2H2,1H3
InChIKey NBBJYMSMWIIQGU-UHFFFAOYSA-N

Propionaldehyde - Physico-chemical Properties

Molecular FormulaC3H6O
Molar Mass58.08
Density0.805 g/mL at 25 °C (lit.)
Melting Point-81 °C (lit.)
Boling Point46-50 °C (lit.)
Flash Point−16°F
JECFA Number83
Water Solubility540 g/L (20 ºC)
Solubility soluble in chloroform; miscible with alcohol and ether
Vapor Presure18.77 psi ( 55 °C)
Vapor Density2 (vs air)
AppearanceLiquid
Specific Gravity0.815 (20/4℃)
ColorWhite
Exposure LimitACGIH: TWA 20 ppm
Merck14,7823
BRN506010
Storage ConditionStore at
StabilityStable. Highly flammable. Incompatible with oxidizing agents, strong acids, strong bases.
SensitiveAir Sensitive
Explosive Limit2.3-21%(V)
Refractive Indexn20/D 1.362(lit.)
Physical and Chemical PropertiesColorless transparent flammable liquid with asphyxiating and irritating odor.
melting point -81 ℃
boiling point 47.9 ℃
relative density 0.7970
refractive index 1.3619
flash point -7.22 ~-9.44 ℃
UseFor the preparation of synthetic fiber, rubber accelerator and antioxidant, can also be used as anti-freezing agent, lubricant, dehydrating agent

Propionaldehyde - Risk and Safety

Risk CodesR11 - Highly Flammable
R36/37/38 - Irritating to eyes, respiratory system and skin.
R41 - Risk of serious damage to eyes
R37/38 - Irritating to respiratory system and skin.
R20/22 - Harmful by inhalation and if swallowed.
Safety DescriptionS9 - Keep container in a well-ventilated place.
S16 - Keep away from sources of ignition.
S29 - Do not empty into drains.
UN IDsUN 1275 3/PG 2
WGK Germany1
RTECSUE0350000
TSCAYes
HS Code29121900
Hazard Class3
Packing GroupII
ToxicityLD50 orally in rats: 1.4 g/kg; LC for rats in air: 8000 ppm (Smyth)

Propionaldehyde - Upstream Downstream Industry

Downstream Products2,3,5-Collidine
Propionic acid
2,2-Bis(hydroxymethyl)propionic acid
Imidacloprid
2-Methyl-2-pentenoic acid

Propionaldehyde - Nature

Open Data Verified Data

colorless transparent flammable liquid with asphyxiating irritating odor and moderate toxicity. The relative density was 0.7970. Melting Point 81 °c. Boiling point 47.9 °c. Flash point (Open Cup)-7. 22 ~-9. 44 ℃. Ignition point: 220 ℃. Refractive index (n2(0)1. 3619, viscosity (25 ℃)0.320mPa · s. Specific heat capacity (20 °c) 2.1856J/(g. °C). Heat of vaporization (0.1 MPa)896J/g. Vapor pressure (20 C) 34.4kPa. Surface tension 21.8 mN/m (20 °c).

Last Update:2025-06-10 22:55:16

Propionaldehyde - Preparation Method

Open Data Verified Data
  1. propylene oxide isomerization method 1,2 A propylene oxide in the presence of chromium vanadium catalyst by gas phase isomerization.
  2. The carbonyl synthesis method consists of a one-step reaction of ethylene with carbon monoxide and hydrogen. Initially, carbonyl drill was used as a catalyst at high pressure (14.7~19.6 MPa). In recent years, rhodium-phosphine complexes have been used as catalysts. The reaction temperature is 100 ℃ and the pressure is 1. 27-1. 47MPa. The method has no isomer and is simple to separate. In addition, there are propanol oxidation method and acrolein hydrogenation method.
Last Update:2022-01-01 10:16:20

Propionaldehyde - Application

Open Data Verified Data

important organic raw materials, can be used for the preparation of alkyd resin, high efficiency and low toxicity of pesticide herbicides, pesticides, antifreeze, fungicides, rubber accelerator and sedative drugs. It can also be used as a chain terminator for the polymerization of ethylene.

Last Update:2025-08-19 16:24:40

Propionaldehyde - Safety

Open Data Verified Data
  • moderate toxicity. The skin, eyes, mouth, nasal mucosa have a stimulating effect, long-term inhalation or inhalation of a large number of asphyxiating symptoms. Rat oral ld501400 mg/kg.LC8000 × 10 -6, Operation Site should maintain good ventilation, the operator should wear protective equipment.
  • sealed packaging with aluminum drum, 160kg per barrel. According to the provisions of flammable and toxic chemicals storage and transportation.
Last Update:2022-01-01 10:16:22

Propionaldehyde - Reference Information

Open Data Unverified Data
FEMA2923 | PROPIONALDEHYDE
olfactory threshold (Odor Threshold)0.001ppm
LogP0.59 at 25℃
NIST chemical information Information provided by: webbook.nist.gov (external link)
EPA chemical information Information provided by: ofmpub.epa.gov (external link)
content analysis determined by content analysis in "acetaldehyde (03401). The amount of sample taken is changed to 750mg. In the calculation, 0.5mol/L sulfuric acid solution per mL is equivalent to 29.04mg of propionaldehyde (C3H6O).
toxicity LD50 orally in rats: 1.4 g/kg; LC for rats in air: 8000 ppm (Smyth)
usage limit FEMA(mg/kg): soft drink 3.9; Cold drink 12; Candy 11; Baked food 13. Moderate limit (FDA § 172.515,2000).
use mainly used to prepare alkyd resin, rubber accelerator and antioxidant, herbicide, pesticide, antifungal agent, propionic acid, propanol, propylamine, etc.
GB 2760-1996 stipulates that spices are allowed to be used. Mainly used to prepare apple, cherry, chocolate and onion flavors.
Propionaldehyde is an important raw material for fine chemicals. It is mainly used to produce intermediates such as n-propanol, propionic acid, trimethylol ethane, and proparaldehyde oxime, and further produce alkyd resins, pesticides, herbicides and pesticides, The drugs Mian Ertong and ethyl thiazine are also widely used in the production of fine chemicals in coatings, plastics, food, textile, feed, and rubber additives. It can also be used as a chain terminator for ethylene polymerization.
n-propionaldehyde is an intermediate of the insecticides imidacloprid, acetamiprid, and pentene cyanothrin. It is also an intermediate of medicine mierton and pyrimethamine.
used to make synthetic fibers, rubber accelerators and anti-aging agents, etc., can also be used as antifreeze, lubricant, dehydrating agent, etc.
used to produce propanol, propionic acid and trimethylethane, Used to make synthetic resin, rubber accelerator and anti-aging agent.
Production method The preparation method is based on the catalytic oxidation of propanol to obtain propionaldehyde, or the carbonyl synthesis method using ethylene, carbon monoxide, and hydrogen as raw materials. Cobalt or rhodium phosphine complex is the catalyst. If cobalt compound is used as catalyst, the reaction temperature is 100~200 ℃, and the pressure is 20~30MPa, which is carried out in a non-polar solvent. If rhodium phosphine complex is used as catalyst, low pressure synthesis method can be used. Reaction equation: CH2 = CH2 + CO + H2 [catalyst] → CH3CH2CHO
although there are many preparation methods for propionaldehyde, industrial production did not begin until the early 1950s. in 1975, the United carbide company of the United States built the first large-scale plant with an annual output of 45,000 t using rhodium-phosphine as catalyst and low-pressure carbonyl synthesis of ethylene to propionaldehyde, and the low-pressure carbonyl synthesis method gradually became the main method and development direction of propionaldehyde production. Of the total production capacity of 230,000 t in the United States, Japan and Western Europe in 1981, more than 95% were produced by low-pressure carbonyl synthesis. 1. The carbonyl synthesis method is formed by the one-step reaction of ethylene, carbon monoxide and hydrogen. It was initially carried out under high pressure (14.7-19.6MPa) using cobalt carbonyl as a catalyst. In recent years, a synthesis method using rhodium phosphine complex as catalyst has been developed. The reaction temperature is 100 ℃ and the pressure is 1.27-1.47MPa. The method has no isomers and is easy to separate. 2. propylene oxide isomerization method 1,2-propylene oxide is obtained by gas phase isomerization in the presence of chromium vanadium catalyst. In addition, there are propanol oxidation and acrolein hydrogenation. Propylene is directly oxidized with palladium chloride as a catalyst to produce propionaldehyde, a 0.5-1.5% by-product of acetone. When the reaction temperature of palladium chloride content in the catalyst is increased, the proportion of propionaldehyde by-product can be increased to 50%.
It is obtained by oxidizing n-propanol with dichromate. n-propanol vapor is obtained by passing through a copper catalyst at high temperature.
category flammable liquid
toxicity classification poisoning
acute toxicity oral-rat LD50: 1410 mg/kg; Oral-mouse LD50: 800 mg/kg
stimulation data eyes-rabbit 20 mg/24 hours moderate; Skin-rabbit 5000 mg moderate
explosive hazard characteristics blastable when mixed with air
flammability hazard characteristics flammability in case of open flame, high temperature and oxidant; Combustion produces stimulating smoke
storage and transportation characteristics warehouse ventilation and low temperature drying; separate from oxidant
fire extinguishing agent dry powder, dry sand, carbon dioxide, foam, 1211 fire extinguishing agent
auto-ignition temperature 404 °F
toxic substance data information provided by: pubchem.ncbi.nlm.nih.gov (external link)
Last Update:2024-04-09 19:43:38
Propionaldehyde
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Propionaldehyde
Downstream Products for Propionaldehyde
2,3,5-Collidine
Propionic acid
2,2-Bis(hydroxymethyl)propionic acid
Imidacloprid
2-Methyl-2-pentenoic acid
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