1,3-Dichloro-5,5-dimethylhydantoin CAS 118-52-5

Introduction:Basic information about 1,3-Dichloro-5,5-dimethylhydantoin CAS 118-52-5, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.

1,3-Dichloro-5,5-dimethylhydantoin Basic information

Product Name:1,3-Dichloro-5,5-dimethylhydantoin
Synonyms:DCDMH;DANTOIN;DACTIN;DICHLORO-DIMETHYL-HYDANTOINE;1,3-DICHLORO-5,5-DIMETHYL-2,4-IMIDAZOLIDINEDIONE;1,3-DICHLORO-5,5-DIMETHYLHYDANTOIN;1,3-DICHLORO-5,5-DIMETHYLHYDANTOINE;1,3-dichloro-5,5’-methylhydantoin
CAS:118-52-5
MF:C5H6Cl2N2O2
MW:197.02
EINECS:204-258-7
Product Categories:Water Ttreatment Chemicals;Imidazolines/ImidazolidinesBuilding Blocks;Halogenated Heterocycles;Heterocyclic Building Blocks;Imidazolines/Imidazolidines;Water treatment chemicals;Miscellaneous;Pyridines;water treatment
Mol File:118-52-5.mol

1,3-Dichloro-5,5-dimethylhydantoin Chemical Properties

Melting point 132-134 °C (lit.)
Boiling point 214.7±23.0 °C(Predicted)
density 1,5 g/cm3
vapor pressure 0.003Pa
refractive index 1.5720 (estimate)
Fp 171 °C
storage temp. Keep in dark place,Sealed in dry,Room Temperature
solubility water: soluble0.21% at 25°C(lit.)
form Crystalline Powder
pka-3.44±0.40(Predicted)
color White
PH4.4 (H2O)(HSDB)
Water Solubility 0.21 g/100 mL (25 ºC)
Sensitive Moisture Sensitive
Sublimation 100 ºC
Merck 14,3065
BRN 146013
Exposure limitsNIOSH REL: TWA 0.2, STEL 0.4, IDLH 5; OSHA PEL: TWA 0.2,STEL/C 0.4 (adopted).
Stability:Stable, but a strong oxidizer - contact with combustible material may lead to fire. Incompatible with reducing agents, acids, strong bases. Moisture sensitive.
InChI1S/C5H6Cl2N2O2/c1-5(2)3(10)8(6)4(11)9(5)7/h1-2H3
InChIKeyKEQGZUUPPQEDPF-UHFFFAOYSA-N
SMILESCC1(C)N(Cl)C(=O)N(Cl)C1=O
LogP-0.94
CAS DataBase Reference118-52-5(CAS DataBase Reference)
EPA Substance Registry System1,3-Dichloro-5,5-dimethylhydantoin (118-52-5)

Safety Information

Hazard Codes Xn,C,O,N
Risk Statements 22-36/37/38-34-8-50-43-31-20/21/22
Safety Statements 26-36-45-36/37/39-17-61
RIDADR UN 1479 5.1/PG 2
OEBC
OELTWA: 0.2 mg/m3, STEL: 0.4 mg/m3
WGK Germany 3
RTECS MU0700000
TSCA TSCA listed
HazardClass 5.1
PackingGroup II
HS Code 29332100
Storage Class5.1B - Oxidizing hazardous materials
Hazard ClassificationsAcute Tox. 4 Oral
Aquatic Acute 1
Aquatic Chronic 1
Ox. Sol. 2
Skin Irrit. 2
Skin Sens. 1
Hazardous Substances Data118-52-5(Hazardous Substances Data)
ToxicityLD50 oral in rabbit: 1520mg/kg
IDLA5 mg/m3

1,3-Dichloro-5,5-dimethylhydantoin Usage And Synthesis

DescriptionDCDMH is a combustible, white powder witha chlorine-like odor. Molecular weight=197.03; Freezing/Melting point=130℃; Flash point=175℃. HazardIdentification (based on NFPA-704 M Rating System):Health 3, Flammability 1, Reactivity 0 Oxidizer, . Waterreactive; slightly soluble; solubility=0.2%.
Chemical PropertiesDCDMH is a combustible, white powder.Chlorine-like odor.
Physical propertiesWhite powder or four-sided crystals from chloroform with a chlorine-like odor. Aqueous solutionsare acidic.
UsesChlorinating agent; disinfectant;laundry bleach; in water treatment; intermediatefor drugs; insecticides; polymerizationcatalyst
UsesDantoin(R) DCDMH is an industrial bleaching agent based on dimethyl hydantoin. This product finds application wherever solid bleach is desired.
UsesDantoin(R) DCDMH LD (low dust) is an industrial bleaching agent based on dimethyl hydantoin. This product finds application wherever solid bleach is desired.
DefinitionMethionine hydroxy analog c. 90%.
General DescriptionWhite powder with a weak chlorine odor. Conflagrates at 414°F (turns brown). Chlorine gas evolves > 410°F.
Air & Water ReactionsSensitive to exposure to light, air, and moisture. Reacts with water or steam to produce toxic and corrosive fumes.
Reactivity Profile1,3-Dichloro-5,5-dimethylhydantoin reacts violently with xylene. 1,3-Dichloro-5,5-dimethylhydantoin is incompatible with strong acids, easily oxidized materials, ammonia salts and sulfides. 1,3-Dichloro-5,5-dimethylhydantoin will react with water or steam to produce toxic and corrosive fumes. At a pH of 9, 1,3-Dichloro-5,5-dimethylhydantoin decomposes completely.
Health Hazard1,3-Dichloro-5,5-dimethylhydantoinpowder in contact with water yieldshypochlorous acid, which is an irritant of theeyes and mucous membranes.
Fire HazardFlash point data for 1,3-Dichloro-5,5-dimethylhydantoin are not available. 1,3-Dichloro-5,5-dimethylhydantoin is probably combustible.
Safety ProfileModerately toxic by ingestion. Mildly toxic by inhalation. A severe slun irritant. Mutation data reported. Avoid excessive contact because of effects of active chlorine on skin. Some of the hydantoins are central nervous system depressants. Mixtures with xylene may explode. Wdl react with water or steam to produce toxic and corrosive fumes. When heated to decomposition it emits toxic fumes of Cl and NOx. See also CHLORIDES.
Synthesis

77-71-4

118-52-5

General procedure for the synthesis of 1,3-dichloro-5,5-dimethylimidazoline-2,4-dione from 5,5-dimethylhydantoin: Preparation of ethyl acetate, tetrahydrofuran and liquid chlorine in the ratio of 1:1:0.7 by volume, as well as 5,5-dimethylglycolide urea, anhydrous sodium carbonate and lanthanum-modified nanoscale Ga/Al composite solid bases in the ratio of 1:1.2:0.15 by mass. The specific dosage was as follows 30 mL of ethyl acetate, 30 mL of tetrahydrofuran, 21 mL of liquid chlorine, 7 g of 5,5-dimethylglycolide, 8.4 g of anhydrous sodium carbonate and 1.05 g of lanthanum-modified nanoscale Ga/Al composite solid base. (1) 7 g of 5,5-dimethylglycolide urea and 8.4 g of anhydrous sodium carbonate were added to a reaction vessel equipped with a spherical condenser tube, magnetically stirred, and reacted for 6 h at room temperature; (2) 1.05 g of lanthanum-modified nanoscale Ga/Al composite solid bases, 30 mL of ethyl acetate, and 30 mL of tetrahydrofuran were added sequentially to the mixture of step (1). Then 21 mL of liquid chlorine was added dropwise at a rate of 60 drops per minute, magnetic stirring was turned on, and the reaction was heated at 100 °C for 2 h. (3) The heated mixture from step (2) was transferred to a microwave reactor for 5 h. The mixture was then heated for 2 h. The mixture was then heated for 2 h. The reaction was then transferred to a microwave reactor for 5 h. After the reaction was completed, the mixture was cooled, filtration was performed, and the filter cake was washed with tetrahydrofuran. The filtrate was rotary evaporated to recover part of ethyl acetate, tetrahydrofuran and lanthanum-modified nanoscale Ga/Al composite solid bases; (4) the residual filtrate from step (3) was poured into pure water under continuous stirring to precipitate the product sufficiently, and pumped and filtered to obtain the crude product. The crude product was successively recrystallized with ethanol and pure water, and then recrystallized with toluene for the second time, and the target product 1,3-dichloro-5,5-dimethylimidazoline-2,4-dione was finally obtained.

Potential ExposureIt is used as a chlorinating agent,disinfectant, biocide, and laundry bleach. It is also used asa polymerization catalyst in making vinyl chloride; andin drug and pesticide synthesis.
First aidIf this chemical gets into the eyes, remove anycontact lenses at once and irrigate immediately for at least15 min, occasionally lifting upper and lower lids. Seek medical attention immediately. If this chemical contacts the skin,remove contaminated clothing and wash immediately withsoap and water. Seek medical attention immediately. If thischemical has been inhaled, remove from exposure, beginrescue breathing (using universal precautions, includingresuscitation mask) if breathing has stopped and CPR if heartaction 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. Donot make an unconscious person vomit. Medical observationis recommended for 24-48 h after breathing overexposure,as pulmonary edema may be delayed. As first aid for pulmonary edema, a doctor or authorized paramedic may consideradministering a corticosteroid spray.
Environmental fateChemical/Physical. Reacts with water (pH 7.0) releasing hypochlorous acid. At pH 9, nitrogenchloride is formed (Windholz et al., 1983).
storage(1) Color Code—Yellow: Reactive Hazard; Storein a location separate from other materials, especially flammables and combustibles. (2) Color Code—White:Corrosive or Contact Hazard; Store separately in a corrosion-resistant location. Prior to working with this chemicalyou should be trained on its proper handling and storage.1,3-Dichloro-5,5-dimethyl-hydantoin must be stored toavoid contact with strong acids (such as sulfuric acid, nitricacid, or hydrochloric acid) and easily oxidized materials(such as ammonium salts and sulfides) since violent reactions occur and poisonous gases can be produced. Store intightly closed containers in a cool, well-ventilated area awayfrom water or steam. 1,3-Dichloro-5,5-dimethyl-hydantoindecomposes with formation of poisonous gases at201-210℃. If 1,3-dichloro-5,5-dimethyl-hydantoin contacts water or steam, it decomposes at lower temperaturesand produces poisonous gases, including chlorine. Sourcesof ignition, such as smoking and open flames, are prohibitedwhere 1,3-dichloro-5,5-dimethyl-hydantoin is used, handled,or stored in a manner that could create a potential fire orexplosion hazard.
ShippingUN1479 Oxidizing solid, n.o.s., Hazard Class:5.1; Labels: 5.1-Oxidizer, Technical Name Required
Purification MethodsPurify it by dissolving in conc H2SO4 and diluting with ice H2O, collect the solid, dry it in a vacuum and recrystallise it from CHCl3. It sublimes at 100o in a vacuum. It exhibits time-dependent hydrolysis at pH 9. [Petterson & Grzeskowiak J Org Chem 24 1414 1959, Beilstein 24 III/IV 1100.]
IncompatibilitiesA strong oxidizer. Contact with waterforms poisonous and corrosive gases. Mixtures with xylenemay explode. Not compatible with moisture (especially hotwater, steam), strong acids; easily oxidized materials (suchas ammonia salts; sulfides, etc.); reducing agents; strongbases; ammonium salts; sulfides. Compounds of thecarboxyl group react with all bases, both inorganic andorganic (i.e., amines) releasing substantial heat, water anda salt that may be harmful. Incompatible with arsenic compounds (releases hydrogen cyanide gas), diazo compounds,dithiocarbamates, isocyanates, mercaptans, nitrides, andsulfides (releasing heat, toxic and possibly flammablegases), thiosulfates and dithionites (releasing hydrogensulfate and oxides of sulfur)
Toxics Screening LevelThe initial threshold screening level (ITSL) for the following bromo- and chloro dimethylhydantoins is 2 μg/m3, based on an 8-hour averaging time.
Waste DisposalIncineration (815.5C/816C,0.5 second for primary combustion; 104.4C/220F, 1.0 second for secondary combustion). The formation of elementalchlorine can be prevented by injection of steam or methaneinto the combustion process. Any nitrogen oxides may beabated by the use of thermal or catalytic devices
References[1] Patent: CN108484506, 2018, A. Location in patent: Paragraph 0016; 0018-0036
[2] Tetrahedron Letters, 2009, vol. 50, # 6, p. 656 - 658
[3] Journal fuer Praktische Chemie (Leipzig), 1926, vol. <2>113, p. 263 Anm.4

1,3-Dichloro-5,5-dimethylhydantoin Preparation Products And Raw materials

Raw materialsHydrochloric acid-->Sodium hypochlorite-->5,5-Dimethylhydantoin-->Ethyl acetate-->Tetrahydrofuran-->Chlorine
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