2696-92-6

Yellow-red liquid or yellow gas.Decomposed by water; dissociates into nitric oxide and chlorine on heating; soluble in fuming sulfuric acid. Nonflammable.

A yellow to yellowish red gas. Liquefies at -5.5°C. Very toxic by inhalation. Noncombustible, but accelerates burning of combustible material. Decomposed by water to form corrosive hydrochloric acid. Vapors heavier than air. Prolonged exposure to fire or heat can cause containers to rupture violently and rocket .

Dissolves into and reacts with moisture in the air or with water to form hydrochloric acid and toxic red oxides of nitrogen.

Nitrosyl chloride is an oxidizing agent. Dissociates into nitric oxide and chlorine on heating. Gives an explosive reaction when sealed in a tube with a residue of acetone and in the presence of platinum catalyst [Chem. Eng. News 35(43):60. 1967]. May react vigorously or explosively if mixed with diisopropyl ether or other ethers in the presence of trace amounts of metal salts [J. Haz. Mat., 1981, 4, 291].

Gas is highly toxic. Inhalation causes severe irritation of respiratory tract and damage to mucous membranes. Delayed effects, which include severe pulmonary edema, may not be apparent for several hours.

Special Hazards of Combustion Products: Very toxic gases are generated when heated

Strong irritant, especially to lungs and mucous membranes.

A nitrocompound used as a reagent, catalyst, bleaching agent, and intermediate for making other chemicals.

First Aid: Move victim to fresh air. Call 911 or emergency medical service. Inhalation: remove victim to fresh air; call a doctor; enforce complete rest until doctor arrives; observe at least 24 hours for delayed effects. Skin or eyes: flush with water for at least 15 minutes. Immediately call a physician and be prepared to transport the victim to a hospital even if no symptoms (such as wheezing, coughing, shortness of breath, or burning in the mouth, throat, or chest) develop. Give artificial respiration if victim is not breathing. Do not use mouth-to-mouth method if victim ingested or inhaled the substance; give artificial respiration with the aid of a pocket mask equipped with a one-way valve or other proper respiratory medical device. Administer oxygen if breathing is difficult. Remove and isolate contaminated clothing and shoes. In case of contact with liquefied gas, thaw frosted parts with lukewarm water. In case of contact with substance, immediately flush skin or eyes with running water for at least 20 minutes. Keep victim warm and quiet. Keep victim under observation. Effects of contact or inhalation may be delayed. Ensure that medical personnel are aware of the material(s) involved and take precautions to protect themselves.

UN1069 Nitrosyl chloride, Hazard Class: 2.3; Labels 2.3-Poisonous gas, 8-Corrosive material; Inhalation Hazard Zone C

Dissolves into and reacts with moisture in the air or with water forming hydrochloric acid and toxic red oxides of nitrogen. Nitrosyl chloride is a strong oxidizer. Violent reaction with strong acids, alkalis (e.g., sodium hydroxide), ammonia, amines, reducing agents, other strong oxidizers. Elevated temperature may cause explosive decomposition. Dissociates into nitric oxide and chlorine on heating. Corrosive to most metals. Attacks some plastics, rubber, and coatings.

Return refillable compressed gas cylinders to supplier. Use a licensed professional waste disposal service to dispose of this material. Dissolve or mix the material with a combustible solvent and burn in a chemical incinerator equipped with an afterburner and scrubber. All federal, state, and local environmental regulations must be observed.

Yellow gas; heavier than air, density 2.3 (air=1); gas density 2.872 g/L; liquefies at -5.55°C; liquid density 1.273 g/mL; freezes at -59.4°C; critical temperature 167°C; reacts with water; soluble in fuming sulfuric acid.

Nitrosyl chloride can be prepared by the reaction of nitric oxide with chlorine: 2NO + Cl₂ → 2ClNO
Also, nitrosyl chloride is produced by the action of chlorine on sodium nitrate; or by the reaction of nitrosyl sulfuric acid with hydrochloric acid: NaNO₃ + Cl₂ → ClNO + NaClO₂ ONHSO₄ + HCl → ClNO + H₂ SO₄
Nitrosyl chloride also is obtained as a byproduct in the manufacture of potassium nitrate from potassium chloride and nitric acid:In the above preparative method, nitrosyl chloride must be separated from nitric acid; otherwise, in the presence of pure and excess nitric acid, it can decompose to nitrogen dioxide and chlorine:2ClNO + HNO₃ → 6NO₂ + Cl₂ +2H₂O
Also, nitrosyl chloride can be synthesized from its elements by heating nitrogen, oxygen and chlorine gas at 400°C: N₂ + O₂ + Cl₂ → 2ClNO
Faraday obtained nitrosyl chloride by dissolving palladium in a mixture of hydrochloric and nitric acids (Faraday, M. Trans. Roy. Soc. (London), Vol. 136, pp. 48, 1846): Pd + HNO₃ + 3HCl → PdCl₂ + ClNO + 2H₂O.

It is an orange gas with a suffocating odour. It has been fractionally distilled at atmospheric pressure in an all-glass, low-temperature still, taking the fraction boiling at -4o and storing it in sealed tubes. Alternatively the gas is dried by CaCl2 and passed through H2SO4 when Cl2 passes on, but NOCl is absorbed to form nitrososulfuric acid (NO.HSO4) which on warming with NaCl evolves pure NOCl [Tilden J Chem Soc 27 630 1874.] It is decomposed by H2O and alkali, and forms compounds with metal chlorides e.g. FeCl3.NOCl. [Coleman Inorg Synth I 55 1939.]