Detail of > 42540-40-9
- MSDS Download

- CAS Number:
- 42540-40-9
- Name:
5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylicacid,7-[[(2R)-2-(formyloxy)-2-phenylacetyl]amino]-3-[[(1-methyl-1H-tetrazol-5-yl)thio]methyl]-8-oxo-,sodium salt (1:1), (6R,7R)-
- Superlist Name:
- Cemandil sodium salt
- Formula:
- C19H18N6O6S2. Na
- Molecular Structure:
![Molecular Structure of 42540-40-9 (5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylicacid,7-[[(2R)-2-(formyloxy)-2-phenylacetyl]amino]-3-[[(1-methyl-1H-tetrazol-5-yl)thio]methyl]-8-oxo-,sodium salt (1:1), (6R,7R)-)](http://www.lookchem.com/300w/2010/0621/42540-40-9.jpg)
- Synonyms:
- 5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylicacid,7-[[(2R)-(formyloxy)phenylacetyl]amino]-3-[[(1-methyl-1H-tetrazol-5-yl)thio]methyl]-8-oxo-,monosodium salt, (6R,7R)- (9CI);5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid,7-[[(formyloxy)phenylacetyl]amino]-3-[[(1-methyl-1H-tetrazol-5-yl)thio]methyl]-8-oxo-,monosodium salt, [6R-[6a,7b(R*)]]-;Bergacef;Cedol;Cefam;Cefamandole formate sodium;Cefamandole nafate;Cefiran;Cemado;Cemandil;Fado;Kefadol;Kefandol;Lampomandol;Mandokef;Mandolsan;O-Formylcefamandole sodium;Sodium7-(D-2-formyloxy-2-phenylacetamido)-3-(1-methyl-1H-tetrazol-5-ylthiomethyl)-3-cephem-4-carboxylate;Sodium O-formylcefamandole;
- Molecular Weight:
- 513.54
- EINECS:
- 255-877-4
- Melting Point:
- 190-193 °C
- Appearance:
- White solid
- Hazard Symbols:
Xn- Risk Codes:
- 36/37/38-42/43
- Safety:
- 26-36Details
Related products
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Reference
- Application of a modified method to the determination of cephalosporins in pharmaceutical formulations by hydroxamic acid formation
- Application of a modified method to the determination of cephalosporins in pharmaceutical formulations by hydroxamic acid formation. Fedai, Inci; Sengun, F. Inci (Eczacilik Fak., Univ. Istanbul, Istanbul, Turk.). Istanbul Univ. Eczacilik Fak. Mecm., 20, 123-30 (English) 1984. CODEN: IEFMA9. ISSN: 0367-7524. DOCUMENT TYPE: Journal CA Section: 64 (Pharmaceutical Analysis) Optimum conditions were evaluated for the reaction of cephalosporins with Ni(II)-hydroxylamine and Fe reagents, and the results were applied to detn. of cephacetrile (I) [10206-21-0], cefamandole [34444-01-4], cefamandole nafate [42540-40-9], cefoperazone [62893-19-0],and ceftizoxime [68401-81-0]. Absorbance was measured at 440-480 nm depending on the cephalosporin. Beer's law was valid in the range 50-250 mg/mL. Relative std. deviations ranged 0.51-1.22% compared to 0.57-26.7% for an official method.
- Determining antibiotics in biological liquids by colorimetry
- Determining antibiotics in biological liquids by colorimetry. Klein, Hilton J. (Dynasciences Corp., USA). Eur. Pat. Appl. EP 134078 A2 13 Mar 1985, 21 pp. DESIGNATED STATES: R: DE, FR, IT, NL. (English). (European Patent Organization). CODEN: EPXXDW. CLASS: ICM: C12Q001-34. APPLICATION: EP 84-303966 12 Jun 1984. PRIORITY: US 83-521857 10 Aug 1983. DOCUMENT TYPE: Patent CA Section: 1 (Pharmacology) A colorimetric method for the detn. of b-lactam ring-contg. antibiotics (cephalosporins and(or) penicillins) in biol. fluids. is described. The method (considered simple, quick, reliable, and inexpensive) involves mixing the test liq. with a b-lactam ring-contg. chromogenic compd. and penicillinase [9001-74-5] (type II) for a predetd. time, measuring (by sight, colorimeter, or spectrophotometer) the amt. of color developed in the test liq., and comparing the color with a color std. Thus, mixing nitrocefin [41906-86-9] as the chromogenic cephalosporin substrate with type II penicillinase resulted in an uninhibited max. reaction (i.e. breaking of the lactam ring and producing of a red color); the addn. of cephalothin [153-61-7], cefazolin [25953-19-9], cephapirin [21593-23-7], cefamandole nafate [42540-40-9], or oxacillin [66-79-5] inhibited the reaction and formation of the red color.
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