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Derivative of acetone
Bromoacetone is an organic compound with the formula CH3COCH2Br. It is a colorless liquid although impure samples appear yellow or even brown. It is a
Bromoacetone
Chemical weapon
PAVA spray (nonivamide), CS gas, CR gas, CN gas (phenacyl chloride), bromoacetone, xylyl bromide, chloropicrin (PS gas) and Mace (a branded mixture). While
Tear_gas
Chemical compound
an alternative to bromoacetone, because acetone, the precursor to bromoacetone, was required for explosives production. Bromoacetone Chloroacetone Iodoacetone
Bromomethyl_ethyl_ketone
Chemical compound
triethylamine tris-hydrofluoride with bromoacetone. This is done through nucleophilic halogen exchange. The bromide in bromoacetone gets replaced by the fluorine
Fluoroacetone
Chemical compound
seconds. Thiobenzophenone, a thioketone that can be isolated as a solid Bromoacetone Chloroacetone Fluoroacetone Iodoacetone International Union of Pure and
Thioacetone
German WWI tear gas
chemical warfare agent consisting of one or more lachrymatory agents: bromoacetone (BA), bromobenzyl cyanide (Camite), bromomethyl ethyl ketone (homomartonite
White Cross (chemical warfare)
White_Cross_(chemical_warfare)
Chemical irritant/tear gas
different types of tear gas have been developed worldwide, e.g., adamsite or bromoacetone, CNB, and CNC. CS has become the most popular due to its strong effect
CS_gas
Organic reaction: addition of a halogen to the alpha carbon of a ketone
((CH3)2C=O), carried out under either acidic or basic conditions, to give bromoacetone: Acidic (in acetic acid): Basic (in aqueous NaOH): In acidic solution
Ketone_halogenation
Organic compound of the form >C(OH)O–
ketones Carbonyl compound alcohol solvent %hemiacetal acetaldehyde methanol 97 acetaldehyde ethanol 91 propionaldehyde methanol 95 bromoacetone methanol 47
Hemiacetal
Chemical compound
may be synthesized on a laboratory scale by a substitution reaction on bromoacetone. It undergoes rapid polymerization, including forming a hemiacetal cyclic
Hydroxyacetone
Chemical compound
hazard class 6.1 (Poison Inhalation Hazard). Its UN number is 1695. Bromoacetone Dichloroacetone Fluoroacetone Hexachloroacetone Use of poison gas in
Chloroacetone
Reaction sequence in organic chemistry
(Stork acylation); and benzylic, allylic/propargylic, α-carbonyl (e.g., bromoacetone), and α-alkoxy (e.g., methoxymethyl chloride) halides alkylate the enamine
Stork_enamine_alkylation
lachrymatory agent or lachrymator). Benzyl chloride Benzyl bromide Bromoacetone (BA) Bromobenzyl cyanide (CA) Bromomethyl ethyl ketone Capsaicin (OC)
List of chemical warfare agents
List_of_chemical_warfare_agents
Chemical compound
with respect to acetone and the acid catalyst: C3H6O + I2 → HI + C3H5IO Bromoacetone Chloroacetone Fluoroacetone Thioacetone "1-iodoacetone". chemsynthesis
Iodoacetone
Chemical compound
dehydrating agent: RCH(OH)CO2H + O=C(CF3)2 → RCH(O)CO2C(CF3)2 + (HO)2C(CF3)2 Bromoacetone Chloroacetone Fluoroacetone Trifluoroacetone Novec 1230 Hexafluorothioacetone
Hexafluoroacetone
asphyxiation Allies Ethyl iodoacetate 1916 Lachrymatory, toxic Allies Bromoacetone 1916 Lachrymatory, irritant Both Monobromomethyl ethyl ketone 1916 Lachrymatory
Chemical weapons in World War I
Chemical_weapons_in_World_War_I
Chemical compound (BrCN)
Austro-Hungarian forces, either as benzene solution or mixture with 25% bromoacetone and 50% benzene. The recommended method to deactivate cyanogen bromide
Cyanogen_bromide
Chemical reaction
biological systems, particularly in marine algae, where dibromoacetaldehyde, bromoacetone, 1, l,l -tribromoacetone, and other related compounds have been found
Carbonyl α-substitution reaction
Carbonyl_α-substitution_reaction
Numbers, classes, and proper shipping names allocated to dangerous goods
1 Beryllium, powder UN 1568 ? (UN No. no longer in use) UN 1569 6.1 Bromoacetone UN 1570 6.1 Brucine UN 1571 4.1 Barium azide, wetted with not less than
List of UN numbers 1501 to 1600
List_of_UN_numbers_1501_to_1600
October 27, 1914, German artillery fired 3,000 7.7 cm shells containing bromoacetone, a tear gas, at Neuve-Chapelle. The first large-scale toxic gas attack
French artillery during World War I
French_artillery_during_World_War_I
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