Quinine hemisulfate hydrate

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Names

[ CAS No. ]:
207671-44-1

[ Name ]:
Quinine hemisulfate hydrate

[Synonym ]:
Quinine hemisulfate
Quinine sulfate

Chemical & Physical Properties

[ Molecular Formula ]:
C₂₀H₂₄N₂O_2.1/₂H₂O₄S_.H₂O

[ Molecular Weight ]:
782.94300

[ Exact Mass ]:
782.35600

[ PSA ]:
192.62000

[ LogP ]:
6.52160

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H315-H319-H335

[ Precautionary Statements ]:
P261-P305 + P351 + P338

[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves

[ Hazard Codes ]:
Xi

[ RIDADR ]:
NONH for all modes of transport

Articles

Interaction of quinine sulfate with anionic micelles of sodium dodecylsulfate: A time-resolved fluorescence spectroscopy at different pH.

Spectrochim. Acta. A. Mol. Biomol. Spectrosc. 148 , 49-59, (2015)

Photophysical behavior and rotational relaxation dynamics of quinine sulfate (QS) in anionic surfactant, sodium dodecylsulfate (SDS) at different pH have been studied using steady state and time resol...

The uptake of trehalose glycolipids by macrophages is independent of Mincle.

ChemBioChem. 16(4) , 683-93, (2015)

Trehalose glycolipids play an important role in the pathogenesis of Mycobacterium tuberculosis and are used as adjuvants for vaccines; however, much still remains unanswered about the mechanisms throu...

In vivo antimalarial activity and mechanisms of action of 4-nerolidylcatechol derivatives.

Antimicrob. Agents Chemother. 59 , 3271-80, (2015)

4-Nerolidylcatechol (1) is an abundant antiplasmodial metabolite that is isolated from Piper peltatum roots. O-Acylation or O-alkylation of compound 1 provides derivatives exhibiting improved stabilit...

4-phenylpiperazine-1-carboximidamide,sulfuric acid,hydrate
1-(diaminomethylidene)-2-dodecylguanidine,sulfuric acid
Quinine sulfate dihydrate
QUININE SULFATE SALT MONOHYDRATE
Quinine Hydrochloride Dihydrate
(5-ethenyl-1-azabicyclo[2.2.2]octan-2-yl)-(6-methoxyquinolin-4-yl)methanol,formic acid,2-hydroxypropanoic acid
4-{[4-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-1-methyl-1H-pyrazol-3-yl]formamido}butanoic acid
rac-1-[(1R,2S)-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)cyclopentanecarbonyl]azetidine-2-carboxylic acid
4-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-4-{[(3-methylpyrazin-2-yl)methyl]carbamoyl}butanoic acid
3-[benzyl(methyl)amino]-2-{[3-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-5-iodophenyl]formamido}propanoic acid
(2R)-1-{3-[({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)methyl]-4-methylpentanoyl}piperidine-2-carboxylic acid
2-[(4-Methylphenyl)sulfinyl]-1,3-dinitrobenzene
3-Methoxy-O,I+/--dimethyl-N-(phenylmethyl)tyrosine
1-[1-(oxetan-3-yl)-1H-1,2,3-triazol-4-yl]ethan-1-amine
3-[3-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-3-methylbutanamido]-2,2,4-trimethylpentanoic acid
3-[2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)pentanamido]-2,2,4-trimethylpentanoic acid

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