14977-61-8 Usage
Chemical Properties
Different sources of media describe the Chemical Properties of 14977-61-8 differently. You can refer to the following data:
1. DEEP RED LIQUID
2. Chromyl chloride is a dark red fuming liquid with a musty, burning odor.
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
Different sources of media describe the Uses of 14977-61-8 differently. You can refer to the following data:
1. In organic oxidations and chlorinations;
as a solvent for chromium oxide; in
making chromium complexes and dyes
2. 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.
3. 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.
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.
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).
General Description
A dark red fuming liquid with a pungent odor. Corrosive to tissue.
Reactivity Profile
Chromyl chloride 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.
Fire Hazard
Behavior in Fire: Vapors are very irritating to eyes and mucous membranes. May increase severity of fire.
Safety Profile
Suspected carcinogen.
Probably a poison by various routes.
Mutation data reported. Corrosive. A strong
irritant. Hydrolyzes to form chromic and
hydrochloric acids. A strong oxidner and
chlorinating agent. Violent reaction with
water. Reacts violently with alcohol, ether,
acetone, turpentine. Ignites or explodes on
contact with nonmetal halides (e.g., disulfur
dichloride, phosphorus trichloride, and
phosphorus tribromide), nonmetal hydrides
(e.g., hydrogen sulfide and hydrogen
phosphide), flowers of sulfur, moist
phosphorus, sodium azide, and urea. During
preparation can violently explode.
Incompatible with ammonia, disulfur
dichloride, organic solvents, phosphorus,
phosphorus trichloride, sodium azide, and
sulfur. When heated to decomposition it
emits toxic fumes of Cl-. See also
CHROMIUM COMPOUNDS.
Potential Exposure
Chromium oxychloride is used in making chromium complexes and dyes; and used in various organic oxidation and chlorination reactions
Shipping
UN1758 Chromium oxychloride, Hazard class: 8; Labels: 8-Corrosive material.
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.
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
Check Digit Verification of cas no
The CAS Registry Mumber 14977-61-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,9,7 and 7 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 14977-61:
(7*1)+(6*4)+(5*9)+(4*7)+(3*7)+(2*6)+(1*1)=138
138 % 10 = 8
So 14977-61-8 is a valid CAS Registry Number.
InChI:InChI=1/2ClH.2Cr.5O/h2*1H;;;;;;;/q;;2*+1;;;;;/p-2/rCl2Cr2O5/c1-3(5,6)9-4(2,7)8
14977-61-8Relevant articles and documents
Thorpe, T. E.
, p. 514 - 515 (1868)
Seddon, Kenneth R.,Thomas, Valerie H.
, (1977)
Oxidation Kinetics of Chromium(III) Chloride
Sole, Kathryn C.,Moolman, Michael B.,Brown, Michael E.
, p. 525 - 530 (2007/10/02)
The kinetic behaviour of anhydrous chromium(III) chloride pellets in oxygen in the temperature range 350-630 deg C has been examined by isothermal and temperature-programmed thermogravimetry and scanning electron microscopy.The reaction starts at ca. 400 deg C under non-isothermal conditions and exhibits a deceleratory rate.Cr2O3 is usually the only solid product detected, although CrO2Cl2 or CrOCl may form under extreme experimental conditions.Isothermal thermogravimetric curves are fitted to a number of kinetic expressions, and statistical analyses are used to identify the rate equation that best describes the experimental data.The examination, by scanning electron microscopy, of cross-sections of partially reacted samples supports the conclusion that the reaction is under chemical control, and occurs at a linearly advancing interface between the reactant and product.The reaction kinetics can best be described by a contracting-geometry rate expression.
Characterisation of Chromium(VI) Oxide Tetrafluoride, CrOF4, and Caesium Pentafluoro-oxochromate(VI) Cs
Hope, Eric G.,Jones, Peter J.,Levason, William,Ogden, J. Steven,Tajik, Mahmoud,Turff, Jeremy W.
, p. 529 - 534 (2007/10/02)
The title compounds have been characterised by elemental analyses, i.r. and u.v. - visible spectroscopy, and some of their reactions are described.Matrix isolation studies on CrOF4 show characteristic i.r. absorptions at 1027.7 and 746.3, 741.6 cm-1 in nitrogen matrices, which are assigned as the A1 (Cr=O) and E(Cr-F) modes respectively of the C4v monomer.Chromium isotope fine structure and relative intensity estimates suggest a bond angle of ca. 106 deg for OCrF.The electronic spectrum of matrix-isolated CrOF4 shows prominent charge-transfer bands at 40000 and 27000 cm-1.
