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13552-44-8

13552-44-8 Structure

13552-44-8 Structure
IdentificationBack Directory
[Name]

4,4'-methylenedianilinium dichloride
[CAS]

13552-44-8
[Synonyms]

Methylenedianiline dihydrochloride.
44METHYLENEDIANILINEDIHYDROCHLORIDE
4,4'-methylenedianilinium dichloride
4,4'-Methylenebisaniline·dihydrochloride
4,4-Methylenedianiline Dihydrochloride Salt
4,4'-methylenebisbenzenamine dihydrochloride
4,4'-Methylenebisaniline·bishydrochloric acid
[EINECS(EC#)]

236-934-2
[Molecular Formula]

C13H16Cl2N2
[MDL Number]

MFCD01670228
[MOL File]

13552-44-8.mol
[Molecular Weight]

271.186
Chemical PropertiesBack Directory
[Appearance]

4,4’-Diaminodiphenylmethane is a pale yel- low crystalline solid (turns light brown on contact with air) with a faint amine-like odor.
[Melting point ]

288 °C
[EPA Substance Registry System]

4,4'-Methylenedianiline dihydrochloride (13552-44-8)
Hazard InformationBack Directory
[General Description]

Light beige fine powder.
[Air & Water Reactions]

May be sensitive to prolonged exposure to air and light. Water soluble.
[Reactivity Profile]

In aqueous solution behaves as an acid. Materials in this group are generally soluble in water. The resulting solutions contain moderate concentrations of hydrogen ions and have pH's of less than 7.0. They react as acids to neutralize bases. These neutralizations generate heat, but less or far less than is generated by neutralization of inorganic acids, inorganic oxoacids, and carboxylic acid. They usually do not react as either oxidizing agents or reducing agents but such behavior is not impossible. Many of these compounds catalyze organic reactions.
[Fire Hazard]

Flash point data for 4,4'-methylenedianilinium dichloride are not available; however, 4,4'-methylenedianilinium dichloride is probably combustible.
[Potential Exposure]

Used as an intermediate and as a curing agent. Approximately 99% of the DDM produced is con- sumed in its crude form (occasionally containing not more than 50% DDM and ply-DDM) at its production site by reac- tion with phosgene in the preparation of isocyanates and poly- isocyanates. These isocyanates and polyisocyanates are employed in the manufacture of rigid polyurethane foams which find application as thermal insulation. Polyisocyanates are also used in the preparation of the semiflexible polyure- thane foams used for automotive safety cushioning. DDM is also used as: an epoxy hardening agent; a raw material in the production of polyurethane elastomers; in the rubber industry as a curative for Neoprene and as an antifrosting agent (anti- oxidant) in footwear; a raw material in the production of Quana nylon; and a raw material in the preparation of poly (amide-imide) resins (used in magnet wire enamels).
[First aid]

If this chemical gets into the eyes, remove any contact lenses at once and irrigate immediately for at least 15 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, includ- ing 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. Give large quantities of water and induce vomiting. Do not make an unconscious person vomit.
[Shipping]

UN2651 4,40 -Diaminodiphenyl methane, Hazard Class: 6.1; Labels: 6.1-Poisonous materials.
[Incompatibilities]

Dust forms and explosive mixture with air. May polymerize in temperatures .125℃ . A weak base. Incompatible with strong oxidizers (chlorates, nitrates, peroxides, permanganates, perchlorates, chlorine, bromine, fluorine, etc.); contact may cause fires or explosions. Keep away from alkaline materials, strong acids. Flammable gas- eous hydrogen may be generated in combination with strong reducing agents, such as hydrides .
[Chemical Properties]

4,4’-Diaminodiphenylmethane is a pale yel- low crystalline solid (turns light brown on contact with air) with a faint amine-like odor.
[Waste Disposal]

Controlled incineration (oxides of nitrogen are removed from the effluent gas by scrubbers and/or thermal devices).
[Uses]

In 1987, about 600 million lb of MDA was produced in the United States captively as a chemical intermediate; additional amounts were also imported. Approximately 99% of theMDAand polymericMDAproduced in the United States, usually by the acid-catalyzed reaction of aniline with formaldehyde, is used as a chemical intermediate in the closedsystem production of methylene diisocyanate (MDI) and polymeric MDI, which are used extensively in the manufacture of rigid semiflexible polyurethane foams for automobile safety cushioning, and also in the production of wire coatings. MDA is also used as a hardener or curing agent for epoxy resins (providing cross-linkages), in the manufacture of various natural and synthetic rubbers as an antioxidant, in the production of polyurethane elastomers, as a curing agent for neoprene, as an antioxidant in rubber, in the preparation of polyamide–imide resins, as a metal deactivator fuel additive (neutralizes the catalytic effect of copper associated with fuel oxidation), and in the production of polymers for synthetic fibers in the textile industry.
Safety DataBack Directory
[Safety Profile]

Confirmed carcinogen with experimental carcinogenic and neoplastigenic data. Mutation data reported. When heated to decomposition it emits toxic fumes of NOx and HCl.
[Hazardous Substances Data]

13552-44-8(Hazardous Substances Data)
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