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Dichloromethane

Dichloromethane Structure
CAS No.
75-09-2
Chemical Name:
Dichloromethane
Synonyms
DCM;METHYLENE CHLORIDE;CH2Cl2;Methylene dichloride;Dichlormethan;F30;Methylenchlorid;DichL;Metaclen;Dichlorome
CBNumber:
CB7740372
Molecular Formula:
CH2Cl2
Molecular Weight:
84.93
MOL File:
75-09-2.mol
MSDS File:
SDS
Modify Date:
2024/7/24 17:31:20

Dichloromethane Properties

Melting point -97 °C
Boiling point 39.8-40 °C mm Hg(lit.)
Density 1.325 g/mL at 25 °C(lit.)
vapor density 2.9 (vs air)
vapor pressure 24.45 psi ( 55 °C)
refractive index n20/D 1.424(lit.)
Flash point 39-40°C
storage temp. room temp
solubility Miscible in ethyl acetate, alcohol, hexanes, methanol, diethyl ether, n-octanol, acetone benzene, carbon tetrachloride, diethyl ether and chloroform.
form Liquid
Specific Gravity 1.329 (20/20℃)
color APHA: ≤10
Odor Odor threshold 160 to 230 ppm
Odor Threshold 160ppm
explosive limit 13-22%(V)
Water Solubility 20 g/L (20 ºC)
λmax λ: 235 nm Amax: 1.00
λ: 240 nm Amax: 0.20
λ: 250 nm Amax: 0.05
λ: 260 nm Amax: 0.02
λ: 340-400 nm Amax: 0.01
Merck 14,6063
BRN 1730800
Henry's Law Constant 2.49 at 30 °C (headspace-GC, Sanz et al., 1997)
Dielectric constant 9.1(20℃)
Exposure limits TLV-TWA 50 ppm (~175 mg/m3) (ACGIH); carcinogenicity: Suspected Human Carcinogen (ACGIH), Animal Sufficient Evidence, Human Inadequate Evidence (IARC).
Stability Volatile
LogP 1.250
CAS DataBase Reference 75-09-2(CAS DataBase Reference)
IARC 2A (Vol. Sup 7, 71, 110) 2017
NIST Chemistry Reference Methylene chloride(75-09-2)
EPA Substance Registry System Methylene chloride (75-09-2)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07,GHS08
Signal word  Warning
Hazard statements  H315-H319-H336-H351
Precautionary statements  P201-P202-P261-P302+P352-P305+P351+P338-P308+P313
Hazard Codes  Xn,T,F,N,C
Risk Statements  40-39/23/24/25-23/24/25-11-67-36/37/38-68/20/21/22-20/21/22-50-37-34
Safety Statements  23-24/25-36/37-45-16-7-26-61-36/37/39
RIDADR  UN 1593 6.1/PG 3
WGK Germany  2
RTECS  PA8050000
3-10
Autoignition Temperature 556 °C
Hazard Note  Harmful
TSCA  Yes
HS Code  2903 12 00
HazardClass  6.1
PackingGroup  III
Toxicity LD50 orally in young adult rats: 1.6 ml/kg (Kimura)
IDLA 2,300 ppm
NFPA 704
4
2 0

Dichloromethane price More Price(106)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) D65100 Dichloromethane contains 40-150?ppm amylene as stabilizer, ACS reagent, ≥99.5% 75-09-2 500ML ₹4167.63 2022-06-14 Buy
Sigma-Aldrich(India) D65100 Dichloromethane contains 40-150?ppm amylene as stabilizer, ACS reagent, ≥99.5% 75-09-2 1L ₹5693.95 2022-06-14 Buy
Sigma-Aldrich(India) PHR1557 Methylene Chloride Pharmaceutical Secondary Standard; Certified Reference Material 75-09-2 3X1.2ML ₹9103.83 2022-06-14 Buy
Sigma-Aldrich(India) D65100 Dichloromethane contains 40-150?ppm amylene as stabilizer, ACS reagent, ≥99.5% 75-09-2 2.5L ₹7469.25 2022-06-14 Buy
Sigma-Aldrich(India) L090000 Dichloromethane 75-09-2 2.5L ₹6040.35 2022-06-14 Buy
Product number Packaging Price Buy
D65100 500ML ₹4167.63 Buy
D65100 1L ₹5693.95 Buy
PHR1557 3X1.2ML ₹9103.83 Buy
D65100 2.5L ₹7469.25 Buy
L090000 2.5L ₹6040.35 Buy

Dichloromethane Chemical Properties,Uses,Production

Description

Dichloromethane is a colorless liquid with an ethereal, but penetrating odor. Its miscibility in alcohol and ether and slight solubility in water has made it an ideal solvent and otherwise extremely versatile chemical. It has been used industrially (solvent and paint remover), as a drug (inhalation anesthetic) and as an agricultural chemical (growth regulator and fertilizer). It is narcotic in high concentrations and carcinogenic. Inhalation exposure to this substance irritates the nose and throat and affects the central nervous system.

Chemical Properties

Dichloromethane is a colorless liquid with a mild, sweet odor. It does not occur naturally in the environment. It is made from methane gas or wood alcohol. Industrial uses of dichloromethane are extensive, as a solvent in paint strippers, as a propellant in aerosols, and as a process solvent in the manufacturing of drugs. dichloromethane is also used as a metal cleaning and fi nishing solvent, and it is approved as an extraction solvent for spices and hops. Exposure to dichloromethane occurs in workplaces by breathing fumes from paint strippers that contain it (check the label), breathing fumes from aerosol cans that use it (check the label), and breathing contaminated air near waste sites.

Physical properties

Clear, colorless liquid with a sweet, penetrating, ethereal odor. Leonardos et al. (1969) determined an odor threshold concentration of 214.0 ppmv. The average least detectable odor threshold concentrations of technical grade methylene chloride in water at 60 °C and in air at 40 °C were 5.6 and 24 mg/L, respectively (Alexander et al., 1982).

Uses

Dichloromethane, also called methylene chloride, is widely used as a solvent, as a degreasing and cleaning reagent, in paint removers, and in extractions oforganic compounds from water for analyses.

Production Methods

Dichloromethane was first prepared by Regnault in 1840 by the chlorination of methyl chloride in sunlight. It became an industrial chemical of importance during the Second World War. Two commercial processes are currently used for the production of dichloromethane—hydrochlorination of methanol and direct chlorination of methane (Rossberg et al., 1986; Holbrook, 1993). The predominant method of manufacturing dichloromethane uses as a first step the reaction of hydrogen chloride and methanol to give methyl chloride. Excess methyl chloride is then mixed with chlorine and reacts to give dichloromethane, with chloroform and carbon tetrachloride as co-products. This reaction is usually carried out in the gas phase thermally but can also be performed catalytically or photolytically. At low temperature and high pressure, the liquid-phase process is capable of giving high selectivity for dichloromethane (Rossberg et al., 1986; Holbrook, 1993).

Reactions

Methylene chloride reacts violently in the presence of alkali or alkaline earth metals and will hydrolyze to formaldehyde in the presence of an aqueous base. Alkylation reactions occur at both functions, thus di-substitutions result.

General Description

Dichloromethane has been tested as a solvent medium for the dipyridine-chromium(VI) oxide. Solubility was reported to be 12.5g/100ml. Role of quantity of TiO2 loading on activated carbon support employed in the photodecomposition of dichloromethane has been investigated.

Air & Water Reactions

Methylene chloride is a colourless liquid with a mild, sweet odour. Somewhat water soluble. Subject to slow hydrolysis which is accelerated by light.

Reactivity Profile

Dichloromethane reacts vigorously with active metals such as lithium, sodium and potassium, and with strong bases such as potassium tert-butoxide. Dichloromethane is incompatible with strong oxidizers, strong caustics and chemically active metals such as aluminum or magnesium powders. The liquid will attack some forms of plastic, rubber and coatings. Dichloromethane reacts with sodium-potassium alloy, (potassium hydrogen + N-methyl-N-nitrosurea), nitrogen tetraoxide and liquid oxygen. Dichloromethane also reacts with titanium. On contact with water Dichloromethane corrodes iron, some stainless steels, copper and nickel. Dichloromethane is incompatible with alkali metals. Dichloromethane is incompatible with amines, zinc and alloys of aluminum, magnesium and zinc. Dichloromethane is liable to explode when mixed with dinitrogen pentaoxide or nitric acid. Mixtures of Dichloromethane in air with methanol vapor are flammable.

Hazard

Toxic. A narcotic. Central nervous systemimpairment and carboxyhemoglobinemia. Possiblecarcinogen.

Health Hazard

Dichloromethane is classified as only slightly toxic by the oral and inhalation routes. Exposure to high concentrations of dichloromethane vapor (>500 ppm for 8 h) can lead to lightheadedness, fatigue, weakness, and nausea. Contact of the compound with the eyes causes painful irritation and can lead to conjunctivitis and corneal injury if not promptly removed by washing. Dichloromethane is a mild skin irritant, and upon prolonged contact (e.g., under the cover of clothing or shoes) can cause burns after 30 to 60 min exposure. Dichloromethane is not teratogenic at levels up to 4500 ppm or embryotoxic in rats and mice at levels up to 1250 ppm.

Fire Hazard

Special Hazards of Combustion Products: Dissociation products generated in a fire may be irritating or toxic.

Flammability and Explosibility

Noncombustible. Dichloromethane vapor concentrated in a confined or poorly ventilated area can be ignited with a high-energy spark, flame, or high-intensity heat source.

Chemical Reactivity

Reactivity with Water No reaction; Reactivity with Common Materials: No reaction; Stability During Transport: Stable; Neutralizing Agents for Acids and Caustics: Not pertinent; Polymerization: Not pertinent; Inhibitor of Polymerization: Not pertinent.

Safety Profile

Confirmed carcinogen with experimental carcinogenic and tumorigenic data. Poison by intravenous route. Moderately toxic by ingestion, subcutaneous, and intraperitoneal routes. Mildly toxic by inhalation. Human systemic effects by ingestion and inhalation: paresthesia, somnolence, altered sleep time, convulsions, euphoria, and change in cardlac rate. An experimental teratogen. Experimental reproductive effects. An eye and severe skin irritant. Human mutation data reported. It is flammable in the range of 12-19% in air but ignition is difficult. It will not form explosive mixtures with air at ordinary temperatures. Mixtures in air with methanol vapor are flammable. It will form explosive mixtures with an atmosphere having a high oxygen content, in liquid O2, N2O4, K, Na, NaK. Explosive in the form of vapor when exposed to heat or flame. Reacts violently with Li, NaK, potassiumtert- butoxide, (KOH + N-methyl-Nnitrosourea). It can be decomposed by contact with hot surfaces and open flame, and then yield toxic fumes that are irritating and give warning of their presence. When heated to decomposition it emits highly toxic fumes of phosgene and Cl-.

Potential Exposure

Methylene chloride is used mainly as a low-temperature extractant of substances which are adversely affected by high temperature. It can be used as a solvent for oil, fats, waxes, bitumen, cellulose acetate; and esters. It is also used as a paint remover; as a degreaser; and in aerosol propellants

Carcinogenicity

Dichloromethane is reasonably anticipated to be a human carcinogen based on sufficient evidence of carcinogenicity from studies in experimental animals.

Shipping

UN1593Dichloromethane, Hazard Class: 6.1; Labels: 6.1-Poisonous materials

Purification Methods

Shake it with portions of conc H2SO4 until the acid layer remains colourless, then wash with water, aqueous 5% Na2CO3, NaHCO3 or NaOH, then water again. Pre-dry with CaCl2, and distil it from CaSO4, CaH2 or P2O5. Store it away from bright light in a brown bottle with Linde type 4A molecular sieves, in an atmosphere of dry N2. Other purification steps include washing with aqueous Na2S2O3, passage through a column of silica gel, and removal of carbonyl-containing impurities as described under Chloroform. It has also been purified by treatment with basic alumina, distillation, and stored over molecular sieves under nitrogen [Puchot et al. J Am Chem Soc 108 2353 1986]. Dichloromethane from Japanese sources contained MeOH as stabiliser which is not removed by distillation. It can, however, be removed by standing over activated 3A Molecular Sieves (note that 4A Sieves cause the development of pressure in bottles), passed through activated Al2O3 and distilled [Gao et al. J Am Chem Soc 109 5771 1987]. It has been fractionated through a platinum spinning band column, degassed, and distilled onto degassed molecular sieves Linde 4A (heated under high vacuum at over 450o until the pressure readings reached the low values of 10-6 mm, ~1-2hours ). Stabilise it with 0.02% of 2,6-di-tert-butyl-p-cresol [Mohammad & Kosower J Am Chem Soc 93 2713 1971]. [Beilstein 1 IV 35.] Rapid purification: Reflux over CaH2 (5% w/v) and distil it. Store it over 4A molecular sieves.

Incompatibilities

Incompatible with strong oxidizers, caustics; chemically active metals, such as aluminum, magnesium powders; potassium, lithium, and sodium; concentrated nitric acid causing fire and explosion hazard. Contact with hot surfaces or flames causes decomposition producing fumes of hydrogen chloride and phosgene gas. Attacks some forms of plastics, rubber and coatings. Attacks metals in the presence of moisture.

Waste Disposal

Consult with environmental regulatory agencies for guidance on acceptable disposal practices. Generators of waste containing this contaminant (≥100 kg/mo) must conform to EPA regulations governing storage, transportation, treatment, and waste disposal. Incineration, preferably after mixing with another combustible fuel; care must be exercised to assure complete combustion to prevent the formation of phosgene; an acid scrubber is necessary to remove the halo acids produced.

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