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Name |
TIQUIZIUM BROMIDE |
EINECS | 1312995-182-4 |
CAS No. | 71731-58-3 | Density | N/A |
PSA | 56.48000 | LogP | 2.36720 |
Solubility | N/A | Melting Point |
278-281° (dec) |
Formula | C19H24 N S2 . Br | Boiling Point | N/A |
Molecular Weight | 410.442 | Flash Point | N/A |
Transport Information | N/A | Appearance | N/A |
Safety | Poison by subcutaneous, intravenous and intraperitoneal routes. Moderately toxic by ingestion. An experimental teratogen. Experimental reproductive effects. When heated to decomposition it emits toxic fumes of Br−, NOx, and SOx. | Risk Codes | N/A |
Molecular Structure | Hazard Symbols | N/A | |
Synonyms |
2H-Quinolizinium,3-(di-2-thienylmethylene)octahydro-5-methyl-, bromide, (5R,9aR)-rel- (9CI);2H-Quinolizinium, 3-(di-2-thienylmethylene)octahydro-5-methyl-, bromide,trans-; HS 902; HSR 902; Thiaton; Tiquizium bromide |
Article Data | 1 |
IUPAC Name:(5R,9aR)-7-(dithiophen-2-ylmethylidene)-5-methyl-1,2,3,4,6,8,9,9a-
octahydroquinolizin-5-ium bromide(71731-58-3)
Synonyms: Tiquizium bromide ; (5R,9aR)-7-(dithiophen-2-ylmethylidene)-5-methyl-1,2,3,4,6,8,9,9a-octahydroquinolizin-5-ium bromide ; Tiquizium ; 2H-Quinolizinium, 3-(di-2-thienylmethylene)octahydro-5-methyl-, bromide, (5R,9aR)-rel- (9CI) ; 2H-Quinolizinium, 3-(di-2-thienylmethylene)octahydro-5-methyl-, bromide, trans- ; HS 902;HSR 902 ; Thiaton
CAS:71731-58-3
MF: C19H24BrNS2
MW: 410.43
Mol File: 71731-58-3.mol
Melting point :246 ~ 248 ℃
Appearance: Tiquizium bromide (71731-58-3) is prism crystals.
1.Tiquizium bromide (71731-58-3) is antispasmodic, which can be obtained from 2 - hydroxyethyl-pyridine of the raw material;
2.Tiquizium bromide (71731-58-3) have good effects on spasm, gastric secretion inhibition and anti-ulcer caused by anti-acetylcholine of parasympathetic nerve endings.
Organism | Test Type | Route | Reported Dose (Normalized Dose) | Effect | Source |
dog | ld50 | intraperitoneal | 56700ug/kg (56.7mg/kg) | sense organs and special senses: mydriasis (pupillary dilation): eye | oyo yakuri. pharmacometrics. vol. 23, pg. 1, 1982. |
dog | ld50 | intravenous | 14200ug/kg (14.2mg/kg) | sense organs and special senses: mydriasis (pupillary dilation): eye | oyo yakuri. pharmacometrics. vol. 23, pg. 1, 1982. |
dog | ld50 | oral | 662mg/kg (662mg/kg) | sense organs and special senses: mydriasis (pupillary dilation): eye | oyo yakuri. pharmacometrics. vol. 23, pg. 1, 1982. |
dog | ld50 | subcutaneous | 129mg/kg (129mg/kg) | sense organs and special senses: mydriasis (pupillary dilation): eye | oyo yakuri. pharmacometrics. vol. 23, pg. 1, 1982. |
mouse | ld50 | intraperitoneal | 83700ug/kg (83.7mg/kg) | sense organs and special senses: mydriasis (pupillary dilation): eye | oyo yakuri. pharmacometrics. vol. 23, pg. 1, 1982. |
mouse | ld50 | intravenous | 10300ug/kg (10.3mg/kg) | sense organs and special senses: mydriasis (pupillary dilation): eye | oyo yakuri. pharmacometrics. vol. 23, pg. 1, 1982. |
mouse | ld50 | oral | 578mg/kg (578mg/kg) | sense organs and special senses: mydriasis (pupillary dilation): eye | oyo yakuri. pharmacometrics. vol. 23, pg. 1, 1982. |
mouse | ld50 | subcutaneous | 82100ug/kg (82.1mg/kg) | sense organs and special senses: mydriasis (pupillary dilation): eye | oyo yakuri. pharmacometrics. vol. 23, pg. 1, 1982. |
rat | ld50 | intraperitoneal | 70500ug/kg (70.5mg/kg) | sense organs and special senses: mydriasis (pupillary dilation): eye | oyo yakuri. pharmacometrics. vol. 23, pg. 1, 1982. |
rat | ld50 | intravenous | 11400ug/kg (11.4mg/kg) | sense organs and special senses: mydriasis (pupillary dilation): eye | oyo yakuri. pharmacometrics. vol. 23, pg. 1, 1982. |
rat | ld50 | oral | 1177mg/kg (1177mg/kg) | sense organs and special senses: mydriasis (pupillary dilation): eye | oyo yakuri. pharmacometrics. vol. 23, pg. 1, 1982. |
rat | ld50 | subcutaneous | 169mg/kg (169mg/kg) | sense organs and special senses: mydriasis (pupillary dilation): eye | oyo yakuri. pharmacometrics. vol. 23, pg. 1, 1982. |
Poison by subcutaneous, intravenous and intraperitoneal routes. Moderately toxic by ingestion. An experimental teratogen. Experimental reproductive effects. When heated to decomposition it emits toxic fumes of Br−, NOx, and SOx.