Online Database of Chemicals from Around the World

Acrolein
[CAS# 107-02-8]

List of Suppliers
Capot Chemical Co., Ltd. China Inquire  
+86 (571) 8558-6718
+86 13336195806
capotchem@gmail.com
sales@capotchem.com
QQ chat
Chemical manufacturer
chemBlink standard supplier since 2006
Wuhan Ruiji Chemical Co., Ltd. China Inquire  
+86 (27) 8325-6046
+86 13871221857
sales@ruijichemical.com
Chemical manufacturer
chemBlink standard supplier since 2008
Hubei Xinjing New Material Co.,Ltd. China Inquire  
+86 (27) 8349-6459
+86 13871595401
emmaxinjing@gmail.com
hbxj8@xinjingchem.com
Chemical manufacturer
chemBlink standard supplier since 2008
Hefei TNJ Chemical Industry Co., Ltd. China Inquire  
+86 (551) 6541-8684
sales@tnjchem.com
Chemical manufacturer since 2001
chemBlink standard supplier since 2010
BOC Sciences USA Inquire  
+1 (631) 485-4226
info@bocsci.com
Chemical manufacturer
chemBlink standard supplier since 2010
The Dow Chemical Company USA Inquire  
+1 (989) 633-1706
fmdcigs@dow.com
Chemical manufacturer
chemBlink standard supplier since 2012
Hangzhou Chemtech Inductry Co., Ltd. China Inquire  
+86 (571) 5671-5668
info@zjchemtech.com
Chemical manufacturer since 2013
chemBlink standard supplier since 2014
Leap Chem Co., Ltd. China Inquire  
+86 (852) 3060-6658
market19@leapchem.com
QQ chat
Chemical manufacturer since 2006
chemBlink standard supplier since 2015
Complete supplier list of Acrolein
Identification
Classification Organic raw materials >> Aldehyde
Name Acrolein
Synonyms 2-Propen-1-one; 2-Propenal; Acrylaldehyde; Acrylic aldehyde
Molecular Structure CAS # 107-02-8, Acrolein, 2-Propen-1-one, 2-Propenal, Acrylaldehyde, Acrylic aldehyde
Molecular Formula C3H4O
Molecular Weight 56.06
CAS Registry Number 107-02-8
EC Number 203-453-4
SMILES C=CC=O
Properties
Density 0.8389
Melting point -87.7 ºC
Boiling point 52.7 ºC
Refractive index 1.402
Flash point -26 ºC
Water solubility Soluble. 21.25 g/100 mL
Safety Data
Hazard Symbols symbol symbol symbol symbol   GHS02;GHS06;GHS05;GHS09 Danger    Details
Hazard Statements H225-H330-H300-H311-H314-H400-H410    Details
Precautionary Statements P210-P233-P240-P241-P242-P243-P260-P262-P264-P264+P265-P270-P271-P273-P280-P284-P301+P316-P301+P330+P331-P302+P352-P302+P361+P354-P303+P361+P353-P304+P340-P305+P354+P338-P316-P317-P320-P321-P330-P361+P364-P363-P370+P378-P391-P403+P233-P403+P235-P405-P501    Details
Hazard Classification
up    Details
HazardClassCategory CodeHazard Statement
Flammable liquidsFlam. Liq.2H225
Acute hazardous to the aquatic environmentAquatic Acute1H400
Skin corrosionSkin Corr.1BH314
Acute toxicityAcute Tox.3H311
Acute toxicityAcute Tox.1H330
Acute toxicityAcute Tox.2H300
Chronic hazardous to the aquatic environmentAquatic Chronic1H410
Acute toxicityAcute Tox.3H301
Serious eye damageEye Dam.1H318
Acute toxicityAcute Tox.2H330
Specific target organ toxicity - repeated exposureSTOT RE1H372
Acute toxicityAcute Tox.2H310
Skin corrosionSkin Corr.1AH314
Specific target organ toxicity - single exposureSTOT SE3H335
CarcinogenicityCarc.2H351
Transport Information UN 1092
SDS Available
up Discovory and Applicatios
Acrolein, also known by its systematic name propenal, is a highly reactive unsaturated aldehyde with the molecular formula C₃H₄O. It was first identified in the 19th century by the decomposition of fats and glycerol, where it was noted for its strong, pungent odor. Acrolein’s reactivity, due to its conjugated carbonyl and alkene groups, has made it a valuable compound in industrial and chemical applications. Although acrolein was initially considered a byproduct, its unique properties have established it as a precursor for multiple synthetic pathways in modern chemistry.

Structurally, acrolein consists of a three-carbon chain with a double bond between the first and second carbons and an aldehyde group on the first carbon. This structure makes it highly electrophilic, reacting readily with nucleophiles, and susceptible to polymerization. These properties allow acrolein to be an effective intermediate in various synthesis processes, though its reactivity also necessitates careful handling. It is typically produced via the oxidation of propylene, a method that allows for large-scale production with controlled yields.

Acrolein is widely used in the synthesis of methionine, an essential amino acid in animal feed that supports growth and metabolism. In this application, acrolein’s reactivity enables it to form intermediates that are further processed into methionine, making it a vital component of the agricultural industry. Acrolein is also used as a biocide, particularly in water treatment systems, where its potent reactivity can eliminate bacteria, algae, and other organisms. This application is especially common in industrial water systems and oil extraction operations, where acrolein helps maintain system efficiency by preventing microbial growth.

In polymer chemistry, acrolein is a building block for numerous specialty polymers and resins. Through polymerization, acrolein forms polyacrolein, a material with applications in adhesives, coatings, and specialty packaging. Furthermore, acrolein derivatives are used in the production of plastics and synthetic fibers, where they impart desired structural properties. Despite its many applications, acrolein is known for its toxicity and environmental impact, necessitating stringent regulations and careful monitoring in its production and use.

The discovery and development of acrolein have contributed significantly to various fields, including agriculture, polymer science, and industrial water treatment. Its versatility and reactivity continue to drive its importance in chemical synthesis and industry, even as research focuses on safe and sustainable handling practices for this valuable compound.
Market Analysis Reports
List of Reports Available for Acrolein
Related Products
9-Acridinecarboxylic acid hydrate  3,6-Acridinediamine sulfate (2:1)  Acridine hydrochloride  9-Acridinemethanol  Acridine Orange 10-nonyl bromide  9-Acridone  Acriflavine hydrochloride  Acriflavine hydrochloride  Acrinathrin  Acrivastine  Acrolein diethyl acetal  Acrolein dimethyl acetal  Acronycine  Acrylamide  2-Acrylamide-2-methylpropanesulfonic acid  Acrylamide-styrene copolymer  4-Acrylamidobutanoic acid  6-Acrylamidohexanoic Acid  2-Acrylamido-2-methylpropanesulfonic acid-acrylic acid copolymer  2-Acrylamido-2-methyl-1-propanesulfonic acid sodium salt