EU/US Properties Organoleptics Cosmetics Suppliers Safety Safety in use Safety references References Other Blenders Uses Occurrence Synonyms Articles Notes
 

quinine bisulfate
cinchonan-9-ol, 6'-methoxy-, (8a,9R)-, sulfate (1:1) (salt)

Supplier Sponsors

Name:(5-ethenyl-1-azabicyclo[2.2.2]octan-7-yl)-(6-methoxyquinolin-4-yl)methanol; sulfuric acid
CAS Number: 549-56-4Picture of molecule3D/inchi
ECHA EINECS - REACH Pre-Reg:208-970-9
FDA UNII:M201HC068W
MDL:MFCD03939590
Molecular Weight:422.50142000
Formula:C20 H26 N2 O6 S
BioActivity Summary:listing
NMR Predictor:Predict (works with chrome or firefox)
Category:flavoring agents
 
US / EU / FDA / JECFA / FEMA / FLAVIS / Scholar / Patent Information:
Google Scholar:Search
Google Books:Search
Google Scholar: with word "volatile"Search
Google Scholar: with word "flavor"Search
Google Scholar: with word "odor"Search
Perfumer and Flavorist:Search
Google Patents:Search
US Patents:Search
EU Patents:Search
Pubchem Patents:Search
FEMA Number:2975 quinine bisulfate
FDA:No longer provide for the use of these seven synthetic flavoring substances
FDA Mainterm (SATF):549-56-4 ; QUININE BISULFATE
 
Physical Properties:
Appearance:pale yellow to brown crystals (est)
Food Chemicals Codex Listed: No
Boiling Point: 495.90 °C. @ 760.00 mm Hg (est)
Vapor Pressure:0.000000 mmHg @ 25.00 °C. (est)
Flash Point: 489.00 °F. TCC ( 253.70 °C. ) (est)
logP (o/w): 3.440 (est)
Shelf Life: 12.00 month(s) or longer if stored properly.
Storage:refrigerate in tightly sealed containers.
Soluble in:
 alcohol
 glycerin
 water, 1.782e+005 mg/L @ 25 °C (est)
 water, 1.08E+04 mg/L @ 25 °C (exp)
 
Organoleptic Properties:
Odor Strength:none
Odor Description:at 100.00 %. odorless
Odor and/or flavor descriptions from others (if found).
 
Cosmetic Information:
None found
 
Suppliers:
BOC Sciences
For experimental / research use only.
quinine hydrogen sulphate
Penta International
QUININE BISULFATE
Santa Cruz Biotechnology
For experimental / research use only.
Quinine Bisulfate
Sigma-Aldrich: Aldrich
For experimental / research use only.
Quinine bisulfate
 
Safety Information:
Preferred SDS: View
European information :
Most important hazard(s):
Xi - Irritant
R 36/37/38 - Irritating to eyes, respiratory system, and skin.
R 42/43 - May cause sensitization by inhalation and skin contact.
S 02 - Keep out of the reach of children.
S 22 - Do not breath dust.
S 26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S 36/37 - Wear suitable protective clothing and gloves.
S 45 - In case of accident or if you feel unwell seek medical advice immediately.
 
Hazards identification
 
Classification of the substance or mixture
GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)
None found.
GHS Label elements, including precautionary statements
 
Pictogram
 
Hazard statement(s)
None found.
Precautionary statement(s)
None found.
Oral/Parenteral Toxicity:
Not determined
Dermal Toxicity:
Not determined
Inhalation Toxicity:
Not determined
 
Safety in Use Information:
Category: flavoring agents
Recommendation for quinine bisulfate usage levels up to:
 not for fragrance use.
 
Use levels for FEMA GRAS flavoring substances on which the FEMA Expert Panel based its judgments that the substances are generally recognized as safe (GRAS).
The Expert Panel also publishes separate extensive reviews of scientific information on all FEMA GRAS flavoring substances and can be found at FEMA Flavor Ingredient Library
publication number: 3
 average usual ppmaverage maximum ppm
baked goods: --
beverages(nonalcoholic): 95.00000100.00000
beverages(alcoholic): --
breakfast cereal: --
cheese: --
chewing gum: --
condiments / relishes: --
confectionery froastings: --
egg products: --
fats / oils: --
fish products: --
frozen dairy: --
fruit ices: --
gelatins / puddings: --
granulated sugar: --
gravies: --
hard candy: --
imitation dairy: --
instant coffee / tea: --
jams / jellies: --
meat products: --
milk products: --
nut products: --
other grains: --
poultry: --
processed fruits: --
processed vegetables: --
reconstituted vegetables: --
seasonings / flavors: --
snack foods: --
soft candy: --
soups: --
sugar substitutes: --
sweet sauces: --
 
Safety References:
EPI System: View
NLM Developmental and Reproductive Toxicity:Search
EPA Substance Registry Services (TSCA):549-56-4
EPA ACToR:Toxicology Data
EPA Substance Registry Services (SRS):Registry
Laboratory Chemical Safety Summary :11069
National Institute of Allergy and Infectious Diseases:Data
WGK Germany:2
(5-ethenyl-1-azabicyclo[2.2.2]octan-7-yl)-(6-methoxyquinolin-4-yl)methanol; sulfuric acid
Chemidplus:0000549564
 
References:
 (5-ethenyl-1-azabicyclo[2.2.2]octan-7-yl)-(6-methoxyquinolin-4-yl)methanol; sulfuric acid
NIST Chemistry WebBook:Search Inchi
Canada Domestic Sub. List:549-56-4
Pubchem (cid):11069
Pubchem (sid):134978198
 
Other Information:
(IUPAC):Atomic Weights of the Elements 2009
(IUPAC):Atomic Weights of the Elements 2009 (pdf)
Videos:The Periodic Table of Videos
tgsc:Atomic Weights use for this web site
(IUPAC):Periodic Table of the Elements
FDA Substances Added to Food (formerly EAFUS):View
CHEMBL:View
HMDB (The Human Metabolome Database):HMDB40183
FooDB:FDB019895
ChemSpider:View
Wikipedia:View
RSC Learn Chemistry:View
Formulations/Preparations:
•quinidine sulfate contains 82% of quinidine base by weight . •quinidine sulfate available capsules, contain 100 mg of the drug; tablets of quinidine polygalacturonate contain 275 mg, equivalent to 200 mg of quinidine sulfate. prepn for slow absorption are also available as 300 mg extended release tablet of quinidine sulfate & a 324 mg tablet of gluconate. quinidine sulfate is also available as an injection in 1 ml ampule containing 200 mgml. the necessary dose is diluted to 800 mg50 ml in 5% glucose solution and is injected at the rate of 16 mgmin, with continuous observation of the patient & of the ecg. •oral tablets extended release 324 mg (equivalent to quinidine 202 mg), quinaglute dura-tabs, berlex, quinatime, cmc; 330 mg (equivalent to quinidine 206 mg), duraquine (with povidone), warner chilcott; parenteral injection, 80 mg (equivalent to quinidine 50 mg) per ml, quinidine gluconate injection (with edetate disodium and phenol). lilly quinidine gluconate •oral tablets 275 mg (equivalent to quinidine sulfate 200 mg), cardioquin (with povidone; scored), purdue frederick. quinidine polygalacturonate •oral tablets, 200 mg, 300 mg, quinora, key; tablets, extended-released, 300 mg, quinidex extentabs, robins quinidine sulfate •capsules and tablets 100, 200, and 300 mg. controlled release tablets, 300 mg. ampules, 200 mgml. •quinidine sulfate is available as tablets (100 to 300 mg) capsules 200, and 300 mg. 300 mg substained release tablets (quinidex) are available, as is an injection (200 mgml). preparations of the gluconate and polygalacturonate salts are also marketed.
 
Potential Blenders and core components note
None Found
 
Potential Uses:
None Found
 
Occurrence (nature, food, other):note
 not found in nature
 
Synonyms:
 cinchonan-9-ol, 6'-methoxy-, (8a,9R)-, sulfate (1:1) (salt)
 cinchonan-9-ol, 6'-methoxy-, sulfate (1:1) (salt)
(5-ethenyl-1-azabicyclo[2.2.2]octan-7-yl)-(6-methoxyquinolin-4-yl)methanol; sulfuric acid
(6-methoxy-quinolin-4-yl)-(5-vinyl-1-aza-bicyclo[2.2.2]oct-2-yl)-methanol
6'-methoxycinchonan-9-ol sulfate (1:1)
8alpha,9R-6'-methoxycinchonan-9-ol sulfate (1:1) salt
6'-methoxycinchonan-9-ol sulfate, (8a,9R)-, (1:1)
8a,9R-6'-methoxycinchonan-9-ol, sulfate (1:1) salt
 quinidine bisulfate
 quinidine, sulfate (2:1) (salt)
 quinine hydrogen sulfate
 quinine hydrogen sulphate
 quinine sulfate (1:1) salt
 quinine sulphate
 quinine, sulfate (1:1) (salt)
 

Articles:

 None found yet.
 
Notes:
Bitter flavouring Used in tonics and bitter drinks Quinine is a natural white crystalline alkaloid having antipyretic, antimalarial, analgesic, anti-inflammatory properties and a bitter taste. It is a stereoisomer of quinidine which, unlike quinine, is an anti-arrhythmic. Though it has been synthesized in the lab, the bark of the cinchona tree is the only known natural source of quinine. Quinine was the first effective treatment for malaria caused by Plasmodium falciparum, appearing in therapeutics in the 17th century. It remained the antimalarial drug of choice until the 1940s, when other drugs replaced it. (Wikipedia)
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