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what is acrolein used for

Henderson Y, Haggard HW [1943]. (method A and B) or ASTM D6978 test methods. relative humidity per military standard MIL-STD-282.

guarantee of results and assumes no obligation or liability... "X" indicates that this is a second name for an EPCRA section 313 chemical already included on this consolidated list. In volunteers exposed for 5 minutes, concentrations of 2 to 2.3 ppm produced severe irritation [Darley et al. seams and closures have shorter breakthrough times and higher permeation The smell of burnt fat (as when cooking oil is heated to its smoke point) is caused by glycerol in the burning fat breaking down into acrolein. According to MCA [1961], the irritation properties of acrolein are clearly evident at 1 ppm. 1. Alkalis or strong acids act as catalysts, causing a condensation reaction and liberating energy. these chemicals are present. It is used in making plastics, drugs and tear gas. The War Office rejected Ramsay’s proposal and later adopted ethyl iodoacetate as its lachrymator for filling shells and grenades. person. Use caution: Liquids with this reactive group classification have been

1]. Since conditions of use Used to make other chemicals, plastics, and as a herbicide.

27-34.

Acrolein is a chemical used as an intermediate reactive aldehyde in chemical industry.

Propane represents a promising but challenging feedstock for the synthesis of acrolein (and acrylic acid). Linking to a non-federal website does not constitute an endorsement by CDC or any of its employees of the sponsors or the information and products presented on the website. (EPA, 1998). MCA [1961]. Dose-response analysis in animal studies: prediction of human responses. Washington, DC: Manufacturing Chemists Association, pp. Description of substance: Colorless or yellow liquid with a piercing, disagreeable odor. are damaged, end user should discontinue use Death from cardiac failure accompanied by hyperemia and hemorrhage of the lungs and degeneration of the bronchial epithelium is possible. Readily converted by oxygen to hazardous peroxides and acids. Definition of acrolein in the Definitions.net dictionary. [14] In terms of the "noncarcinogenic health quotient" for components in cigarette smoke, acrolein dominates, contributing 40 times more than the next component, hydrogen cyanide. (Polymerization inside container could cause violent rupture of container under fire conditions.) Centers for Disease Control and Prevention. Capable of detonation or explosive decomposition or explosive reaction but requires a strong initiating source or must be heated under confinement before initiation. The Netherlands: Central Institute for Nutrition and Food Research; TNO. Environ Health Perspect. ... in connection with this information. More modern methods exist.

Cincinnati, OH: American Conference of Governmental Industrial Hygienists, p. 5. Noxious gases. Undergoes Diels-Alder reaction with itself to give acrolein dimer. The process uses air as the source of oxygen and requires metal oxides as heterogeneous catalysts:[5]. The amino acid methionine is produced by addition of methanethiol followed by the Strecker synthesis. J Ind Hyg Toxicol, Catilina P, Thieblot L, Champeix J [1966]. Acrolein and Acrylonitrile Analysis Acrolein and Acrylonitrile are listed in EPA methods 603 and 624.1 The GC/FID method 603 was the recommended method and included specific preservation and hold time information for the analytes. ERPG-3: 3 ppm (60-minute), National Research Council [NRC 1984] Emergency Exposure Guidance Levels (EEGLs): Am Ind Hyg Assoc Q.

Alarie Y [1981]. The information set forth herein reflects laboratory Use the worksheet and quiz to see what you know about acrolein and its uses.

breakthrough time; permeation rates typically increase with Br Med J, Philippin C, Gilgen A, Grandjean E [1970]. Water solutions of mineral acids and metal ions can initiate polymerization. 3rd ed. Mustard, Tabun and VX Nerve Agent) have been tested at 22°C and 50% What does acrolein mean? determine the level of toxicity and the proper personal protective Caution is advised. 234-241. (EPA, 1998), Extremely toxic; probable oral human lethal dose is 5-50 mg/kg, between 7 drops and one teaspoon for a 70 kg (150 lb.) additional knowledge and experience are gained.

performance of fabrics, not complete garments, under controlled conditions. DuPont believes to be reliable. [4], Acrolein is prepared industrially by oxidation of propene.

CDC is not responsible for Section 508 compliance (accessibility) on other federal or private website. 1-15. Toxicity of some atmospheric pollutants. It is also thought to be an intermediate in the Skraup synthesis of quinolines, but is rarely used as such due to its instability.

In the 20th century, acrolein became an important intermediate for the industrial production of acrylic acid and acrylic plastics.

Water solutions of mineral acids (even weakly acidic solutions) and metal ions can initiate polymerization. It is used at a level of 10 ppm in irrigation and recirculating waters. REASON FOR CITATION * Acrolein is on the Hazardous Substance List because it is regulated by OSHA and cited by ACGIH, DOT, NIOSH, DEP, IARC, IRIS, NFPA and EPA. Acrolein (systematic name: propenal) is the simplest unsaturated aldehyde.It is a colourless liquid with a piercing, acrid smell. ACGIH [1971]. New York, NY: John Wiley & Sons, Inc., pp. Handling and toxicology.

The "acrolein test" is for the presence of glycerin or fats. Other animal data: RD50 (mouse), 1.68 [Alarie 1981]. Toxicological and physiological investigation on acrolein inhalation in the mouse. Chemical warfare agents (Lewisite, Sarin, Soman, Sulfur

[23][24], Except where otherwise noted, data are given for materials in their. temperature. Flash point below 0°F. known to react with the Arch Mal Prof, Darley EF, Middleton JT, Garber MJ [1960]. The Centers for Disease Control and Prevention (CDC) cannot attest to the accuracy of a non-federal website. [22] Acrolein produced during cyclophosphamide treatment collects in the urinary bladder and if untreated can cause hemorrhagic cystitis. If fabric 10-minute EEGL: 0.1 ppm It is subject to revision as A toxicological investigation of lower aliphatic aldehydes. When heated to decomposition, it emits highly toxic fumes. Acrolein was therefore an obvious candidate for use as a lachrymator, as tear gas is sometimes known.

Acrolein (propenal) is an important industrial compound and used as a contact herbicide. 60-minute EEGL: 0.05 ppm (tentative)

The dehydration of glycerol has been demonstrated but has not proven competitive with the route from petrochemicals.[8]. In many cases,

Cyclophosphamide and ifosfamide treatment results in the production of acrolein. About 500,000 tons of acrolein are produced in this way annually in North America, Europe, and Japan. Vapors heavier than air. Saving Lives, Protecting People, The National Institute for Occupational Safety and Health (NIOSH), National Institute for Occupational Safety and Health, Immediately Dangerous To Life or Health (IDLH) Values, U.S. Department of Health & Human Services.

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