Identification | Back Directory | [Name]
LEUCOFORM | [CAS]
613-11-6 | [Synonyms]
LEUCOFORM Valnivudine leucomethylene blue Hydromethylthionine 3,7-Bis(dimethylamino)-10H-phenothiazine N,N,N',N'-Tetramethyl-10H-phenothiazine-3,7-diamine N3,N3,N7,N7-tetramethyl-10H-phenothiazine-3,7-diamine 10H-Phenothiazine-3,7-diamine, N3,N3,N7,N7-tetramethyl- | [Molecular Formula]
C16H19N3S | [MOL File]
613-11-6.mol | [Molecular Weight]
285.41 |
Chemical Properties | Back Directory | [Boiling point ]
491.7±45.0 °C(Predicted) | [density ]
1.201±0.06 g/cm3(Predicted) | [storage temp. ]
Amber Vial, -86°C Freezer, Under inert atmosphere | [pka]
6.62±0.20(Predicted) | [Stability:]
Very unstable to air, keep and handle under inert gas. |
Hazard Information | Back Directory | [Uses]
Leucomethylene blue is the reduced form of methylene blue, and has been used to determine the efficacy in tau aggregation inhibitor therapy for Alzheimer''s disease. | [Definition]
ChEBI: Leucomethylene blue is a member of the class of phenothiazines that is 10H-phenothiazine in which the ring hydrogens at positions 3 and 7 have been replaced by dimethylamino groups. It has a role as a fluorochrome, a bacterial xenobiotic metabolite, a rat metabolite and a mouse metabolite. It is a member of phenothiazines, an aromatic amine and a tertiary amino compound. |
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