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Tretoquinol dl-form hydrochloride

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Name

Tretoquinol dl-form hydrochloride

EINECS N/A
CAS No. 18559-63-2 Density 1.235g/cm3
PSA 80.18000 LogP 2.88190
Solubility N/A Melting Point N/A
Formula C19H23 N O5 . Cl H Boiling Point 533.3°Cat760mmHg
Molecular Weight 381.856 Flash Point 276.3°C
Transport Information N/A Appearance N/A
Safety Poison by intravenous and intraperitoneal routes. An experimental teratogen. Experimental reproductive effects. When heated to decomposition it emits toxic fumes of NOx and HCl. An adrenergic beta-stimulant. See also INOLIN. Risk Codes N/A
Molecular Structure Molecular Structure of 18559-63-2 (Tretoquinol hydrochloride) Hazard Symbols N/A
Synonyms

6,7-Isoquinolinediol,1,2,3,4-tetrahydro-1-(3,4,5-trimethoxybenzyl)-, hydrochloride, (?à)- (8CI); 6,7-Isoquinolinediol,1,2,3,4-tetrahydro-1-[(3,4,5-trimethoxyphenyl)methyl]-, hydrochloride (9CI);6,7-Isoquinolinediol, 1,2,3,4-tetrahydro-1-[(3,4,5-trimethoxyphenyl)methyl]-,hydrochloride, (?à)-;(?à)-Trimetoquinol hydrochloride;1,2,3,4-Tetrahydro-1-(3,4,5-trimethoxybenzyl)-6,7-isoquinolinediolhydrochloride;1-(3,4,5-Trimethoxybenzyl)-6,7-dihydroxy-1,2,3,4-tetrahydroisoquinolinehydrochloride; AQ 110; AQ 110 (pharmaceutical);dl-1-(3,4,5-Trimethoxybenzyl)-6,7-dihydroxy-1,2,3,4-tetrahydroisoquinolinehydrochloride; dl-Trimetoquinol hydrochloride

 

Tretoquinol dl-form hydrochloride Chemical Properties

IUPAC Name: 1-[(3,4,5-Trimethoxyphenyl)methyl]-1,2,3,4-tetrahydroisoquinolin-
2-ium-6,7-diol chloride
The molecular formula of Tretoquinol hydrochloride (CAS NO.18559-63-2) is C19H24ClNO5.

                                
The molecular weight of Tretoquinol hydrochloride (CAS NO.18559-63-2) is 381.850560.
Synonyms of Tretoquinol hydrochloride (CAS NO.18559-63-2): 1,2,3,4-Tetrahydro-1-(3,4,5-trimethoxybenzyl)-6,7-isoquinolinediol ; Inolin ; Trimethoquinol
Index of Refraction: 1.593 
Density: 1.235 g/ml
Flash Point: 276.3 °C
Boiling Point: 533.3 °C

Tretoquinol dl-form hydrochloride Uses

  Tretoquinol hydrochloride (CAS NO.18559-63-2) is used as chemical reagent, organic synthesis, pharmaceutical intermediate.

Tretoquinol dl-form hydrochloride Toxicity Data With Reference

Organism Test Type Route Reported Dose (Normalized Dose) Effect Source
guinea pig LD50 intraperitoneal 660mg/kg (660mg/kg) BEHAVIORAL: CONVULSIONS OR EFFECT ON SEIZURE THRESHOLD

LUNGS, THORAX, OR RESPIRATION: RESPIRATORY DEPRESSION

LUNGS, THORAX, OR RESPIRATION: OTHER CHANGES
European Journal of Pharmacology. Vol. 5, Pg. 303, 1968.
guinea pig LD50 oral > 2gm/kg (2000mg/kg)   European Journal of Pharmacology. Vol. 5, Pg. 303, 1968.
mouse LD50 intraperitoneal 340mg/kg (340mg/kg) BEHAVIORAL: CONVULSIONS OR EFFECT ON SEIZURE THRESHOLD

LUNGS, THORAX, OR RESPIRATION: RESPIRATORY DEPRESSION

LUNGS, THORAX, OR RESPIRATION: OTHER CHANGES
European Journal of Pharmacology. Vol. 5, Pg. 303, 1968.
mouse LD50 intravenous 130mg/kg (130mg/kg) BEHAVIORAL: CONVULSIONS OR EFFECT ON SEIZURE THRESHOLD

LUNGS, THORAX, OR RESPIRATION: OTHER CHANGES

LUNGS, THORAX, OR RESPIRATION: RESPIRATORY DEPRESSION
European Journal of Pharmacology. Vol. 5, Pg. 303, 1968.
mouse LD50 oral > 2gm/kg (2000mg/kg)   European Journal of Pharmacology. Vol. 5, Pg. 303, 1968.
mouse LD50 subcutaneous 480mg/kg (480mg/kg)   Pharmaceutical Chemistry Journal Vol. 18, Pg. 262, 1984.
rat LD50 intraperitoneal 311mg/kg (311mg/kg) BEHAVIORAL: CONVULSIONS OR EFFECT ON SEIZURE THRESHOLD

LUNGS, THORAX, OR RESPIRATION: RESPIRATORY DEPRESSION

LUNGS, THORAX, OR RESPIRATION: OTHER CHANGES
European Journal of Pharmacology. Vol. 5, Pg. 303, 1968.
rat LD50 intravenous 174mg/kg (174mg/kg) BEHAVIORAL: CONVULSIONS OR EFFECT ON SEIZURE THRESHOLD

LUNGS, THORAX, OR RESPIRATION: OTHER CHANGES

LUNGS, THORAX, OR RESPIRATION: RESPIRATORY DEPRESSION
European Journal of Pharmacology. Vol. 5, Pg. 303, 1968.
rat LD50 oral > 2gm/kg (2000mg/kg)   European Journal of Pharmacology. Vol. 5, Pg. 303, 1968.
rat LD50 subcutaneous > 2gm/kg (2000mg/kg)   European Journal of Pharmacology. Vol. 5, Pg. 303, 1968.

Tretoquinol dl-form hydrochloride Safety Profile

Poison by intravenous and intraperitoneal routes. An experimental teratogen. Experimental reproductive effects. When heated to decomposition it emits toxic fumes of NOx and HCl. An adrenergic beta-stimulant. See also INOLIN.

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