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461-72-3

461-72-3 Structure

461-72-3 Structure
IdentificationMore
[Name]

Hydantoin
[CAS]

461-72-3
[Synonyms]

2,4-(3H,5H)-IMIDAZOLEDIONE
2,4-IMIDAZOLIDINEDIONE
2,4-IMIDAZOLINEDIONE
GLYCOLYLUREA
HYDANTOIN
Imidazolidine-2,4-dione
2-hydroxy-2-imidazolin-4(or5)-on
2-Imidazolin-4(or 5)-one, 2-hydroxy-
Imidazole-2,4(3H,5H)-dione
Hydantoin,99%
NSC 922
glycollylurea
2,4-Imidazolidinedione ,2-hydroxy-2-imidazolin-4(or 5)-on ,glycolylurea ,hydantoin
NSC 9226
2,5-Imidazolidinedione
Imidazolidine-2,5-dione
[EINECS(EC#)]

207-313-3
[Molecular Formula]

C3H4N2O2
[MDL Number]

MFCD00005259
[Molecular Weight]

100.08
[MOL File]

461-72-3.mol
Chemical PropertiesBack Directory
[Appearance]

White Solid
[Melting point ]

218-220 °C (lit.)
[Boiling point ]

187.47°C (rough estimate)
[density ]

1.4457 (rough estimate)
[vapor pressure ]

0Pa at 25℃
[refractive index ]

1.5110 (estimate)
[storage temp. ]

Store below +30°C.
[solubility ]

SLIGHTLY SOLUBLE
[form ]

Fine Powder
[pka]

pKa 9.1 (Uncertain)
[color ]

White to light yellow
[Water Solubility ]

SLIGHTLY SOLUBLE
[Merck ]

14,4761
[BRN ]

110598
[InChI]

1S/C3H4N2O2/c6-2-1-4-3(7)5-2/h1H2,(H2,4,5,6,7)
[InChIKey]

WJRBRSLFGCUECM-UHFFFAOYSA-N
[SMILES]

O=C1CNC(=O)N1
[LogP]

-1.69
[CAS DataBase Reference]

461-72-3(CAS DataBase Reference)
[NIST Chemistry Reference]

2,4-Imidazolidinedione(461-72-3)
[EPA Substance Registry System]

461-72-3(EPA Substance)
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P264-P280-P302+P352-P321-P332+P313-P362-P264-P280-P305+P351+P338-P337+P313P
[Hazard Codes ]

Xi
[Risk Statements ]

R36/37/38:Irritating to eyes, respiratory system and skin .
[Safety Statements ]

S24/25:Avoid contact with skin and eyes .
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection .
S27:Take off immediately all contaminated clothing .
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
[WGK Germany ]

3
[RTECS ]

MT8210000
[TSCA ]

Yes
[REACH Registrations]

Inactive
[HS Code ]

29332100
[Storage Class]

11 - Combustible Solids
Raw materials And Preparation ProductsBack Directory
[Raw materials]

Orotic acid-->SYNTHETIC RESIN-->N,N'-Diethylthiourea-->Hydantoic acid-->Isopropyl alcohol-->Benzil
[Preparation Products]

Glycine-->L-Valine-->BANISTERINE MONOHYDRATE-->5-Methoxy-DL-tryptophan-->(S)-2-Amino-3-(6-methoxy-1H-indol-3-yl)-propionic acid-->S-α-cyano-3-phenoxy benzyl alcohol-->Orotic acid monohydrate-->Parabanic acid-->2-(4-Fluorobenzoyl)acetic acid-->4-Chlorobenzalhydantoin-->4-[(2,5-Dioxoimidazolidin-1-yl)methyl]benzonitrile-->1,3-dibromoimidazolidine-2,4-dione-->(5E)-5-[(3-hydroxyphenyl)methylidene]imidazolidine-2,4-dione
Material Safety Data Sheet(MSDS)Back Directory
[msds information]

2,4-Imidazolinedione(461-72-3).msds
Hazard InformationBack Directory
[Description]

Hydantoin is a fundamental structural unit of organic compounds, serving as a building block for the preparation of hydantoin drugs. Hydantoin drugs are a class of anticonvulsants. Compounds such as phenytoin or fosphenytoin incorporate the hydantoin structure and are employed in the treatment of epilepsy.
[Chemical Properties]

White Solid
[Uses]

Reactant for synthesis of: N-benzyl aplysinopsin analogs as anticancer agents1 D-glutamic acid based inhibitors2 Antidiabetic chromonyl-2,4-thiazolidinediones3 GSK-3β inhibitors with brain permeability4 Thiazolidinedione derivatives as 15-PGDH inhibitors5 Radio-sensitizing agents6
[Definition]

ChEBI: Hydantoin is an imidazolidine-2,4-dione.
[Pharmaceutical Applications]

Control of generalized convulsive status epilepticus; prevention and treatment of seizures during neurosurgery; short-term substitute for oral phenytoin.
[Mechanism of action]

Hydantoins are a class of drugs mainly used to treat seizures (anticonvulsant or antiepileptic drugs). Hydantoins reduce seizures by targeting the sodium channel present throughout the nerves. Activation of sodium channels results in the conduction of electrical impulses and the release of neurotransmitters. It could stabilise neuronal membranes by decreasing sodium and calcium ion influx into the neurons. Also decreases post-tetanic potentiation and repetitive discharge.
[Pharmacokinetics]

Completely absorbed after IM administration. Protein binding: 95%–99%. Rapidly and completely hydrolyzed to phenytoin after IM or IV administration. Time of complete conversion to phenytoin: 4 hr after IM injection; 2 hr after IV infusion. Half-life: 8–15 min (for conversion to phenytoin).
Spectrum DetailBack Directory
[Spectrum Detail]

Hydantoin(461-72-3)MS
Hydantoin(461-72-3)1HNMR
Hydantoin(461-72-3)13CNMR
Hydantoin(461-72-3)IR1
Hydantoin(461-72-3)IR2
Hydantoin(461-72-3)Raman
Well-known Reagent Company Product InformationBack Directory
[Acros Organics]

Hydantoin, 99%(461-72-3)
[Alfa Aesar]

Hydantoin, 99%(461-72-3)
[Sigma Aldrich]

461-72-3(sigmaaldrich)
[TCI AMERICA]

Hydantoin,>99.0%(T)(461-72-3)
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