600-25-9 Usage
Description
1-CHLORO-1-NITROPROPANE, also known as Chloronitropropane, is a colorless liquid with an unpleasant odor and lachrymatory properties, which means it can cause tears. It is a flammable substance and is used in various applications across different industries.
Uses
1. Used in Fungicide Applications:
1-CHLORO-1-NITROPROPANE is used as an active ingredient in fungicides for its ability to control and prevent fungal growth, thereby protecting crops and enhancing agricultural productivity.
2. Used in Chemical Synthesis:
1-CHLORO-1-NITROPROPANE is used as an intermediate in the synthesis of various chemicals, including pharmaceuticals and other industrial products, due to its unique chemical properties and reactivity.
3. Used in Industrial Processes:
1-CHLORO-1-NITROPROPANE is utilized in certain industrial processes, such as the production of solvents and other specialty chemicals, where its specific characteristics are advantageous for the desired outcomes.
4. Used in Research and Development:
1-CHLORO-1-NITROPROPANE serves as a valuable compound in research and development for its potential applications in various fields, including material science, pharmaceuticals, and environmental science, as it can be modified and used to create new compounds with specific properties.
Synthesis Reference(s)
The Journal of Organic Chemistry, 42, p. 3764, 1977 DOI: 10.1021/jo00443a034
Air & Water Reactions
Slightly soluble in water [Lawry's].
Reactivity Profile
1-CHLORO-1-NITROPROPANE is sensitive to heat (may be explosive). 1-CHLORO-1-NITROPROPANE is incompatible with oxidizers. 1-CHLORO-1-NITROPROPANE will attack some forms of plastics, rubber and coatings . Combustible: May produce toxic gases, including nitrogen oxides, hydrogen chloride, and carbon monoxide. Will attack some plastics, rubber, and coatings [USCG, 1999].
Fire Hazard
Combustible: May produce toxic gases, including nitrogen oxides, hydrogen chloride, and carbon monoxide. Will attack some plastics, rubber, and coatings.
Safety Profile
Poison by ingestion,
subcutaneous, and possibly other routes.
Moderately toxic by inhalation. Causes
injury to kidneys, liver, and cardiovascular
system. Mutation data reported. Flammable
liquid when exposed to heat, flame (sparks),
and oxidizers. Moderately explosive when
exposed to heat. To fight fire, use alcohol
foam, water, CO2, or dry chemical. When
heated to decomposition it emits toxic
fumes of Cland NOx. See also other
chloropropane entries and CHLORIDES.
Potential Exposure
This compound is used in the synthetic rubber industry; as a component in rubber cements;
and as a fungicide.
Shipping
UN2810 Toxic liquids, organic, n.o.s., Hazard
Class: 6.1; Labels: 6.1-Poisonous materials, Technical
Name Required.
Incompatibilities
May form explosive mixture with air.
Strong oxidizers may cause a fire and explosion hazard.
May explode when exposed to heat.
Waste Disposal
Incineration (816C, 0.5-second
minimum for primary combustion; 1204C, 1.0 second for
secondary combustion) after mixing with other fuel. The formation of elemental chlorine may be prevented by injection
of steam or using methane as a fuel in the process.
Alternatively it may be poured over soda ash, neutralized
and flushed into the sewer with large volumes of water.
Check Digit Verification of cas no
The CAS Registry Mumber 600-25-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,0 and 0 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 600-25:
(5*6)+(4*0)+(3*0)+(2*2)+(1*5)=39
39 % 10 = 9
So 600-25-9 is a valid CAS Registry Number.
InChI:InChI=1/C3H6ClNO2/c1-2-3(4)5(6)7/h3H,2H2,1H3/t3-/m0/s1
600-25-9Relevant articles and documents
Electrooxidative coupling of salts of nitro compounds with halide, nitrite, cyanide, and phenylsulfinate anions
Ilovaisky,Merkulova,Ogibin,Nikishin
, p. 1585 - 1592 (2007/10/03)
Electrolysis of salts of primary and secondary nitro compounds (nitroethane, 1- and 2-nitropropanes, nitrocyclohexane, and nitrocycloheptane) in the presence of excess halide, nitrite, cyanide, and phenylsulfinate anions under undivided and divided amperostatic electrolysis conditions in a two-phase medium (CH2Cl2/H2O) produces geminal nitrohalides (35-85% yields), dinitro compounds (15-51%), nitronitriles (6-27%), and nitrosulfones (50-70%). The salts of secondary nitro compounds form the products of oxidative coupling with halide and phenylsulfinate anions under the undivided electrolysis conditions. In all other cases, divided electrolysis is required.
