Aloglutamol

Aloglutamol
Clinical data
Other names	Tasto; trometamolgluconate aluminium
ATC code	A02AB06 (WHO) ;
Identifiers
	IUPAC name Dihydroxyaluminium gluconate; Tris(hydroxymethyl)aminomethane (1:1);
CAS Number	13755-41-4 ;
ChemSpider	28426726 ;
UNII	I670EI8M2N;
CompTox Dashboard (EPA)	DTXSID601027584 ;
Chemical and physical data
Formula	C10H24NO12
Molar mass	350.297 g·mol−1
3D model (JSmol)	Interactive image;
	SMILES C([C@H]([C@H]([C@@H]([C@H](C(=O)O[Al](O)O)O)O)O)O)O.C(C(CO)(CO)N)O;
	InChI InChI=1S/C6H12O7.C4H11NO3.Al.2H2O/c7-1-2(8)3(9)4(10)5(11)6(12)13;5-4(1-6,2-7)3-8;;;/h2-5,7-11H,1H2,(H,12,13);6-8H,1-3,5H2;;2*1H2/q;;+3;;/p-3/t2-,3-,4+,5-;;;;/m1..../s1 ; Key:GJJYZOBRHIMORS-GQOAHPRESA-K ;
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Aloglutamol is an antacid, an aluminium compound.^[1] It is a salt of aluminium, gluconic acid, and tris.^[2]^[3] It is usually given orally in doses of 0.5 to 1 g.^[4] Proprietary names include Altris, Pyreses, Tasto and Sabro.^[4]^[5]

References

^ Dikshith TS (1 November 2010). Handbook of Chemicals and Safety. Taylor & Francis US. p. 69. ISBN 978-1-4398-2060-5. Retrieved 29 April 2012.
^ Bonanno A, Tonini GM, de Marinis S (1978). "[Use of Aloglutamol in uremic patients on dialysis (author's transl]". Urologia Internationalis (in French). 33 (4): 213–221. doi:10.1159/000280201. PMID 705977.
^ Aloglutamol, Comparative Toxicogenomics Database
^ ^a ^b Martindale W (1993). The Extra Pharmacopoeia. Royal Pharmaceutical Society of Great Britain, Dept. of Pharmaceutical Sciences, Pharmaceutical Press. p. 869. ISBN 978-0-85369-300-0. Retrieved 29 April 2012.
^ Negwer M, Scharnow HG (2001). Organic-chemical drugs and their synonyms: (an international survey). Wiley-VCH. p. 157. ISBN 978-3-527-30247-5. Retrieved 29 April 2012.

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