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Allyl aldehyde = acrolein

Acrolein Allyl aldehyde, propenal) CH2 CHCHO -26 278 2.8-31.0 0.8 1.9 53 Colourless/yellow liquid Pungent unpleasant odour Water soluble Irritant Can polymerize exothermically with strong alkalis, heat or light Can form peroxides... [Pg.180]

CAS Number Acraldehyde Acrolein Acryladehyde Acrylaldehyde Acrylic aldehyde Allyl aldehyde Aqualin Aquilin, Magnacide H Propenal 107-02-8... [Pg.749]

Synonyms Acraldehyde Acrylaldehyde /rans-Acrolein Acrylic aldehyde AI3-24160 Allyl aldehyde Aqualin Aqualine Biocide BRN 1701567 Caswell No. 009 CCRIS 3278 Crolean EINECS 203-453-4 Ethylene aldehyde Magnacide Magnacide H NSC 8819 Papite Propenal 2-Propenal Prop-2-en-l-al 2-Propen-l-one Propylene aldehyde RCRA waste number P003 Slimicide UN 1092. [Pg.73]

ACROLEIN Acraldehyde, Acrylic Aldehyde, Allyl Aldehyde, Ethylene Aidehide, 2-Propenal, Acrylaldehyde Flammable Liquid, III 3 3 2 ... [Pg.95]

SYNS ACQUINITE ACRALDEHYDE ACROLEINA (ITALIAN) ACROLEINE pUTCH, FRENCH) ACRYLALDEHYD (GERMAN) ACRYLALDEHYDE ACRYLIC ALDEHYDE AKROLEIN (CZECH) AKROLEINA (POLISH) ALDEHYDE ACRYLIQUE (FRENCH) ALDEIDE ACRILICA (ITALIAN) ALLYL ALDEHYDE AQUAUNE BIOCIDE CROLEAN ETHYLENE ALDEHYDE MAGNACIDE H NSC-8819 ... [Pg.25]

When allyl alcohol, Ai-propen-ol-3, is oxidized carefully allyl aldehyde is obtained. As this aldehyde yields acrylic acid on further oxidation it is more commonly known as acrylic aldehyde and also as acrolein. [Pg.168]

C.16) 2-Propenal, acry/aldehyde, prop-2-enal, acrolein, acrylic aldehyde, allyl aldehyde [107-02-8]... [Pg.116]

DiaUyl Allyl bydrozid Acrolein (hydrocarbon) C cohol). (aldehyde). [Pg.301]

Acrolein 9- kro-le-9n [ISV acr- (fr. L acr, acer) - - L o/ere] (1857) (propenal, acrylic or allyl aldehyde) n. CH2=CHCHO. A liquid derived from the oxidation of allyl alcohol or propylene, used as an intermediate in the production of polyester resins and polyurethanes. It is an unsaturated liquid aldehyde with a bp of 52° C. It possesses a very pungent odor, and has strong lachrymatory properties. [Pg.19]

Allylmagnesium bromide, 41, 49 reaction with acrolein, 41, 49 5-Allyl-l,2,3,4,5-pentachlorocyclopen-tadiene, 43, 92 Allyltriphenyltin, 41, 31 reaction with phenyllithium, 41, 30 Aluminum chloride, as catalyst, for isomerization, 42, 9 for nuclear bromination and chlorination of aromatic aldehydes and ketones, 40, 9 as Friedel-Crafts catalyst, 41, 1 Amidation, of aniline with maleic anhydride, 41, 93... [Pg.106]

Several methods and reaction pathways have been reported for the conversion of glycerol in the literature, such as etherification, esterification [1], and oxidation [2], Via ionic dehydration acetol [3] and acrolein can be produced. The radical steps result in aldehydes, allyl alcohol, etc. [4], If the dehydration is followed by a hydrogenation step, propanediols (1,2- or 1,3-) can be obtained [5-6]. [Pg.437]

See other pages where Allyl aldehyde = acrolein is mentioned: [Pg.94]    [Pg.207]    [Pg.174]    [Pg.367]    [Pg.304]    [Pg.94]    [Pg.207]    [Pg.174]    [Pg.367]    [Pg.304]    [Pg.250]    [Pg.213]    [Pg.173]    [Pg.1169]    [Pg.1459]    [Pg.841]    [Pg.288]    [Pg.96]    [Pg.96]    [Pg.249]    [Pg.96]    [Pg.19]    [Pg.267]    [Pg.11]    [Pg.157]    [Pg.572]    [Pg.841]    [Pg.555]    [Pg.328]    [Pg.329]    [Pg.331]    [Pg.241]    [Pg.847]    [Pg.467]    [Pg.278]    [Pg.53]    [Pg.128]    [Pg.1530]   


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Acrolein

Acroleine

Aldehyde allylic

Aldehydes acrolein

Aldehydes allylation

Allyl aldehyde

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