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XANTHACRIDINE

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Name

XANTHACRIDINE

EINECS N/A
CAS No. 86-40-8 Density N/A
PSA 55.92000 LogP 0.14830
Solubility N/A Melting Point N/A
Formula C14H14 N3 . Cl Boiling Point N/A
Molecular Weight 259.738 Flash Point N/A
Transport Information N/A Appearance N/A
Safety A human poison by intravenous route. Poison experimentally by intraperitoneal, intravenous, and subcutaneous routes. Human mutation data reported. When heated to decomposition it emits very toxic fumes of NOx and Cl. Risk Codes N/A
Molecular Structure Molecular Structure of 86-40-8 (3,6-DIAMINO-10-METHYLACRIDINIUM CHLORIDE) Hazard Symbols N/A
Synonyms

3,6-Diamino-10-methylacridiniumchloride (7CI); Acridinium, 3,6-diamino-10-methyl-, chloride (8CI,9CI); 2,8-Diamino-10-methylacridiniumchloride; 3,6-Diamino-N-methylacridinium chloride; Avlon; Burnol; C.I. 46000;Chromoflavine

 

XANTHACRIDINE Chemical Properties

Product Name: Xanthacridine (CAS NO.86-40-8)


Molecular Formula: C14H14ClN3 
Molecular Weight: 259.7341g/mol
Mol File: 86-40-8.mol
Einecs: 201-668-8
H-Bond Donor: 2
H-Bond Acceptor: 3

XANTHACRIDINE Toxicity Data With Reference

Organism Test Type Route Reported Dose (Normalized Dose) Effect Source
bird - wild LD50 oral 56200ug/kg (56.2mg/kg)   Archives of Environmental Contamination and Toxicology. Vol. 12, Pg. 355, 1983.
cat LDLo intravenous 7353ug/kg (7.353mg/kg) SENSE ORGANS AND SPECIAL SENSES: OTHER CHANGES: OLFACTION

SENSE ORGANS AND SPECIAL SENSES: OTHER: EYE

LUNGS, THORAX, OR RESPIRATION: OTHER CHANGES
Lancet. Vol. 196, Pg. 838, 1919.
dog LDLo intravenous 25mg/kg (25mg/kg) BEHAVIORAL: CONVULSIONS OR EFFECT ON SEIZURE THRESHOLD

VASCULAR: BP LOWERING NOT CHARACTERIZED IN AUTONOMIC SECTION

LUNGS, THORAX, OR RESPIRATION: OTHER CHANGES
Journal of Pharmacology and Experimental Therapeutics. Vol. 38, Pg. 145, 1930.
frog LDLo subcutaneous 800mg/kg (800mg/kg) PERIPHERAL NERVE AND SENSATION: SPASTIC PARALYSIS WITH OR WITHOUT SENSORY CHANGE

CARDIAC: OTHER CHANGES

LUNGS, THORAX, OR RESPIRATION: OTHER CHANGES
Zeitschrift fuer die Gesamte Experimentelle Medizin. Vol. 12, Pg. 195, 1921.
guinea pig LDLo intraperitoneal 250mg/kg (250mg/kg)   "Abdernalden's Handbuch der Biologischen Arbeitsmethoden." Vol. 4, Pg. 1292, 1935.
guinea pig LDLo intravenous 40mg/kg (40mg/kg)   "Abdernalden's Handbuch der Biologischen Arbeitsmethoden." Vol. 4, Pg. 1292, 1935.
guinea pig LDLo subcutaneous 250mg/kg (250mg/kg)   "Abdernalden's Handbuch der Biologischen Arbeitsmethoden." Vol. 4, Pg. 1292, 1935.
human LDLo intravenous 1500ug/kg (1.5mg/kg)   Journal of Pharmacology and Experimental Therapeutics. Vol. 38, Pg. 145, 1930.
mammal (species unspecified) LD50 intraperitoneal 65mg/kg (65mg/kg)   Journal of Pharmacology and Experimental Therapeutics. Vol. 80, Pg. 217, 1944.
mouse LD50 intravenous 40mg/kg (40mg/kg)   British Journal of Experimental Pathology. Vol. 28, Pg. 1, 1947.
mouse LD50 subcutaneous 14mg/kg (14mg/kg)   British Journal of Experimental Pathology. Vol. 28, Pg. 1, 1947.
mouse LDLo intraperitoneal 11mg/kg (11mg/kg)   Toxicology and Applied Pharmacology. Vol. 23, Pg. 288, 1972.
quail LD50 oral > 100mg/kg (100mg/kg)   Ecotoxicology and Environmental Safety. Vol. 6, Pg. 149, 1982.
rabbit LDLo intravenous 25mg/kg (25mg/kg) BEHAVIORAL: CONVULSIONS OR EFFECT ON SEIZURE THRESHOLD

VASCULAR: BP LOWERING NOT CHARACTERIZED IN AUTONOMIC SECTION

LUNGS, THORAX, OR RESPIRATION: OTHER CHANGES
Journal of Pharmacology and Experimental Therapeutics. Vol. 38, Pg. 145, 1930.

XANTHACRIDINE Consensus Reports

Reported in EPA TSCA Inventory.

XANTHACRIDINE Safety Profile

A human poison by intravenous route. Poison experimentally by intraperitoneal, intravenous, and subcutaneous routes. Human mutation data reported. When heated to decomposition it emits very toxic fumes of NOx and Cl.

XANTHACRIDINE Specification

 Xanthacridine ,its CAS NO. is 86-40-8,the synonyms is Timtec-bb sbb003092 ; 2 8-Diamino-10-methylacridinium chloride hydrochloride ; 3,6-Diamino-10-methylacridinium chloride ; Labotest-bb lt00244810 ; 3,6-Diamino-10-methyl-acridiniuchloride ; Burnol ; Acridinium, 3,6-diamino-10-methyl-, chloride ; Chromoflavine .

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