Detail of > 695-53-4
- CAS Number:
- 695-53-4
- Name:
2,4-Oxazolidinedione,5,5-dimethyl-
- Superlist Name:
- Dimethadione
- Formula:
- C5H7NO3
- Molecular Structure:

- Synonyms:
- AC 1198;5,5-Dimethyloxazolidinedione;5,5-Dimethyl-2,4-oxazolidinedione;5,5-Dimethyl-1,3-oxazolidine-2,4-dione;Nortrimethadione;NSC 30152;Dimethadion;DMO;BAY 1400Z;BAX1400Z;Eupractone;
- Molecular Weight:
- 129.13
- EINECS:
- 211-781-4
- Density:
- 1.204 g/cm3
- Melting Point:
- 77-80 °C(lit.)
- Boiling Point:
- 137 °C / 6mmHg
- Appearance:
- white crystalline powder
- Hazard Symbols:
Xn,
Xi- Risk Codes:
- 20/21/22-40-33-36/37/38
- Safety:
- 22-36-24/25-23-36/37-26Details
- Deleted CAS:
- 60254-97-9
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Reference
- Simultaneous determination of dimethadione and trimethadione by infrared-spectrometry: application for mean intracellular pH measurement
- Simultaneous determination of dimethadione and trimethadione by infrared-spectrometry: application for mean intracellular pH measurement. Zweens, J.; Frankena, Henny (Dep. Physiol., Univ. Groningen, Groningen NL-9712 KZ, Neth.). J. Clin. Chem. Clin. Biochem., 22(10), 641-5 (English) 1984. CODEN: JCCBDT. ISSN: 0340-076X. DOCUMENT TYPE: Journal CA Section: 1 (Pharmacology) A simple IR-spectrometric method for the simultaneous detn. of dimethadione [695-53-4] and trimethadione [127-48-0] in plasma is described. The method is based on the absorption band of the carbonyl group for trimethadione at the wavenumber of 1740 cm-1 and for dimethadione at the wavenumber of 1770 cm-1. The accuracy and precision of the method are excellent; at a dimethadione and trimethadione concn. of 0.5 mmol×L-1 the coeff. of variation for the detn. of both compds. is <1%, which is better than that for the UV spectrometric or gas-liq. chromatog. methods. The method can be used for the detn. of the ratio trimethadione/dimethadione in the clin. setting as a sensitive check of the patient's adherence to therapy. It can also be used for the detn. of dimethadione as an indicator for the mean body intracellular pH.
- The protective effect of cysteine on chemical-induced liver injury in rats
- The protective effect of cysteine on chemical-induced liver injury in rats. Tanaka, Einosuke; Hagino, Sigenobu; Yoshida, Takemi; Kuroiwa, Yukio; Ohno, Hiromitsu; Numata, Hiroshi (Sch. Pharm. Sci., Showa Univ., Tokyo 142, Japan). J. Toxicol. Sci., 9(3), 245-51 (English) 1984. CODEN: JTSCDR. DOCUMENT TYPE: Journal CA Section: 4 (Toxicology) Section cross-reference(s): 1 The possible protective effect of cysteine [52-90-4] on chem.-induced liver injury was studied in rats in vivo and in vitro. There was no increase in the activity of serum glutamic-oxaloacetic transaminase (GOT) [9000-97-9] of rats pretreated with cysteine (1.2 g/kg, orally) followed by 0.25 mL/kg CCl4 [56-23-5], D-galactosamine (GalN) [7535-00-4], or a-naphthylisothiocyanate (ANIT) [551-06-4]. However, rats pretreated with cysteine followed by 0.5 mL/kg CCl4 were not protected. The content of cytochrome P 450 [9035-51-2], activity of aminopyrine N-demethylase [9037-69-8], or serum ratio of 5,5-dimethyl-2,4-oxazolidinedione (DMO) [695-53-4] to trimethadione (TMO) [127-48-0] (DMO/TMO ratio) after CCl4, GalN, or ANIT were not altered by pretreatment with cysteine. However, pretreatment with cysteine prevented changes in the content of cytochrome P 450, activity of aminopyrine N-demethylase, and DMO/TMO ratio in serum as well as the activities of serum GOT and GPT [9000-86-6] when the rats were treated with bromobenzene (BZ) [108-86-1]. The degree of lipid peroxidn. from CCl4 was markedly reduced by the presence of 10-4M cysteine. Thus, cysteine may have a protective effect on chem.-induced liver injury produced via epoxide metabolites.
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