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CAS No 80663-95-2 , Guanidine,N-[(3-iodophenyl)methyl]-

  • Name: Guanidine,N-[(3-iodophenyl)methyl]-
  • Synonyms: m-Iodobenzylguanidine;Guanidine,N-[(3-iodophenyl)methyl]-; (3-Iodobenzyl)guanidine;meta-Iodobenzylguanidine;Guanidine,[(3-iodophenyl)methyl]- (9CI);
  • CAS Registry Number:
  • Flash Point: 184.9°C
  • Boiling Point: 382.1°Cat760mmHg
  • Density: 1.85g/cm3
  • Flash Point: 184.9°C
  • Molecular Weight: 275.0896
  • InChI: InChI=1/2C8H10IN3.H2O4S/c2*9-7-3-1-2-6(4-7)5-12-8(10)11;1-5(2,3)4/h2*1-4H,5H2,(H4,10,11,12);(H2,1,2,3,4)
  • Molecular Formula: C8H10 I N3
  • Molecular Structure:CAS No:80663-95-2 Guanidine,N-[(3-iodophenyl)methyl]-

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80663-95-2 SC-200865 M-IODOBENZYLGUANIDINE 1/2H2SO4

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80663-95-2; 103346-16-3 3-IODOBENZYL-GUANIDINEHEMISULFATE;M-IBG

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80663-95-2 M-IODOBENZYLGUANIDINE HEMISULFATE SALT

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References of Guanidine,N-[(3-iodophenyl)methyl]-
Title: Iobenguane
CAS Registry Number: 80663-95-2
CAS Name: [(3-Iodophenyl)methyl]guanidine
Synonyms: m-iodobenzylguanidine; MIBG
Molecular Formula: C8H10IN3
Molecular Weight: 275.09
Percent Composition: C 34.93%, H 3.66%, I 46.13%, N 15.28%
Literature References: Norepinephrine analog with specific affinity for tissues of sympathetic nervous system and related tumors; prepd as 123I and 131I labeled forms. Prepn and imaging studies: D. M. Wieland et al., J. Nucl. Med. 21, 349 (1980); eidem, US 4584187 (1986). Improved synthesis: P. A. P. M. van Doremalen, A. G. M. Janssen, J. Radioanal. Nucl. Chem. Lett. 96, 97 (1985). Metabolism in man: T. J. Mangner et al., J. Nucl. Med. 27, 37 (1986). HPLC determn in serum and urine: D. Schwabe et al., J. Chromatogr. 487, 177 (1989). Radiopharmacokinetics: S. Ertl et al., Nucl. Med. Commun. 8, 643 (1987). Clinical evaluation of myocardial imaging: D. Fagret et al., Eur. J. Nucl. Med. 15, 624 (1989). Diagnostic use in pheochromocytoma: B. Shapiro et al., J. Nucl. Med. 26, 576 (1985); therapeutic use: M. Krempf et al., J. Clin. Endocrinol. Metab. 72, 455 (1991). Symposia on therapeutic and diagnostic use in neuroblastoma: Advances in Neuroblastoma Research 2, A. E. Evans et al., Eds. (Alan R. Liss, Inc., New York, 1988) p 643-726; Med. Pediatr. Oncol. 15, 157-228 (1987). Review of pharmacology: J. C. Sisson, D. M. Weiland, Am. J. Physiol. Imaging 1, 96-103 (1986); of biodistribution and clinical studies: A. R. Wafelman et al., Eur. J. Nucl. Med. 21, 545-559 (1994); of therapeutic use in neural crest tumors: L. Troncone, V. Rufini, Anticancer Res. 17, 1823-1832 (1997).
 
Derivative Type: Sulfate
Molecular Formula: (C8H10IN3)2.H2SO4
Molecular Weight: 648.26
Percent Composition: C 29.64%, H 3.42%, I 39.15%, N 12.96%, S 4.95%, O 9.87%
Properties: Colorless crystals from water + ethanol, mp 166-167°.
Melting point: mp 166-167°
 
Therap-Cat: Radiolabeled forms as antineoplastic; diagnostic aid (radioactive imaging agent).