General Description
A dark red fuming liquid with a pungent odor. Corrosive to tissue.
Reactivity Profile
CHROMIUM OXYCHLORIDE is a powerful and often violent oxidizing agent. Reacts readily with many inorganic and organic materials in the absence of a dilutent. Contact with hydrogen sulfide or phosphine can cause ignition. Contact with phosphorus tribromide, acetone, ethanol, ether, and turpentine causes ignition. Contact with moist phosphorus or with phosphorus trichloride leads to explosive reaction. Contact with ammonia causes incandescence. Reacts with sodium azide to form chromyl azide, which is explosive in the absence of a dilutent. Causes ignition of flowers of sulfur and of urea on contact. [Bretherick, 1979, p. 822-823].
Hazard
Corrosive to tissue. Strong oxidizing agent.
Skin and upper respiratory tract irritant. Probable
carcinogen.
Health Hazard
Inhalation causes severe irritation of upper respiratory system. Contact with eyes or skin causes irritation and burning. Ingestion causes burning of mouth and stomach.
Potential Exposure
Chromium oxychloride is used in making chromium complexes and dyes; and used in various organic oxidation and chlorination reactions
Fire Hazard
Behavior in Fire: Vapors are very irritating to eyes and mucous membranes. May increase severity of fire.
First aid
If this chemical gets into the eyes, remove any contact lenses at once and irrigate immediately for at least 30 minutes, occasionally lifting upper and lower lids. Seek medical attention immediately. If this chemical contacts the skin, remove contaminated clothing and wash immediately with soap and water. Seek medical attention immediately. If this chemical has been inhaled, remove from exposure, begin rescue breathing (using universal precautions, including resuscitation mask) if breathing has stopped and CPR if heart action has stopped. Transfer promptly to a Medical facility. When this chemical has been swallowed, get medical attention. If victim is conscious, administer water or milk. Do not induce vomiting
Shipping
UN1758 Chromium oxychloride, Hazard class: 8; Labels: 8-Corrosive material.
Incompatibilities
Contact with water is violent and forms hydrochloric and chromic acids, and chlorine gas. A powerful oxidizer. Reacts violently with acetone, alcohol, ammonia, ether, fuels, organic solvents, moist phosphorus, phosphorus trichloride; sodium azide; sulfur, reducing agents; turpentine. Contact with nonmetal halides, such as disulfur dichloride, phosphorus trichloride; and phosphorus tribromide; nonmetal hydrides, such as hydrogen sulfide; hydrogen phosphide, and urea, causes a danger fire and explosion hazard
Description
Chromyl chloride is a dark red fuming liquidwith a musty, burning odor. Molecular weight = 154.90;Specific gravity (H2O:1) =1.91 at 25℃; Boilingpoint =117℃; Freezing/Melting point =-96.5℃; Vaporpressure =20 mmHg at 25℃. Soluble in water(decomposes).
Chemical Properties
Chromyl chloride is a dark red fuming liquid with a musty, burning odor.
Chemical Properties
DEEP RED LIQUID
Physical properties
Dark red, fuming liquid; reddish yellow vapors; musty buring odor; density 1.91 g/mL; freezes at -96.5°C; boils at 117°C; reacts with water; soluble in chloroform, carbon tetrachloride, benzene, carbon disulfide and nitrobenzene.
Uses
Catalyst for polymerization of olefins; oxidation of hydrocarbons; in the Etard reaction for production of aldehydes and ketones; in the preparation of various coordination complexes of Cr.
Uses
Highly spin-polarized chromium dioxide (CrO2) thin films were deposited on 100 TiO2 substrates by chemical vapor deposition using chromyl chloride as a precursor. Chromyl chloride (Cr02C12) reacts with cyclohexane solvent at 75 OC to give a dark precipitate along with chlorocyclohexane and a small amount of cyclohexene (in 10.0 and ca. 0.3% yields based on chromium). Chromyl chloride, CrO2C12, oxidizes cyclooctane, isobutane, and toluene under mild conditions (25-60" C). The reactions give chlorinated products (chlorocyclooctane, tert- butyl chloride, and benzyl chloride) and a dark chromium-containing precipitate. Used for Organic oxidations and chlorination, chromium coordination complexes, catalyst for polymerization of olefins. Chromyl chloride in carbon tetrachloride solution reacts in the cold with cyclohexene, cyclopentene, and 1-hexene to give the various isomeric chlorohydrins as the major products.
Uses
In organic oxidations and chlorinations;
as a solvent for chromium oxide; in
making chromium complexes and dyes
Definition
A dark red covalent liquid
prepared either by distilling a dry mixture
of potassium dichromate and sodium chloride
with concentrated sulfuric acid or by
the action of concentrated sulfuric acid on
chromium(VI) oxide dissolved in concentrated
hydrochloric acid. Chromyl chloride
is hydrolyzed by water, and with solutions
of alkalis it undergoes immediate hydrolysis
to produce chromate ions. It is used as
an oxidizing agent in organic chemistry.
Chromyl chloride oxidizes methyl groups
at the ends of aromatic side chains to aldehyde
groupings (étard’s reaction).
Preparation
Chromyl chloride is prepared by reacting chromium(III) chloride with hydrochloric acid:
CrO3 + 2HCl → CrO2Cl2 + H2O
Also, it may be prepared by warming potassium dichromate with potassium chloride in concentrated sulfuric acid:
K2Cr2O7 + 4KCl + 3H2SO4 → 2Cr2O2Cl2 + 3K2SO4 + 3H2O.
storage
Color Code—White: Corrosive or ContactHazard; Store separately in a corrosion-resistant location.Prior to working with Chromium chloride you should betrained on its proper handling and storage. A regulated,marked area should be established where this chemical ishandled, used, or stored in compliance with OSHAStandard 1910.1045. Chromium chloride must be stored toavoid contact with water since violent reactions occur,releasing poisonous materials including chromic acid,hydrogen chloride, chromic chloride, and chlorine. Store intightly closed containers in a cool, well-ventilated areaaway from flammable and combustible materials, ammonia, alcohol and turpentine, and other incompatible materials listed above.
Purification Methods
Purify it by distillation under reduced pressure. It hydrolyses violently with H2O and is a powerful oxidant which explodes with P, and ignites in contact with S, NH3, EtOH and many organic compounds. TOXIC.
