Tolterodine tartrate

Modify Date: 2025-08-23 00:41:24

Tolterodine tartrate Structure
Tolterodine tartrate structure
 Common Name Tolterodine tartrate
CAS Number 124937-52-6 Molecular Weight 475.574
Density 1.003 g/cm3 Boiling Point 442.2ºC at 760 mmHg
Molecular Formula C26H37NO7 Melting Point 205-210ºC
MSDS Chinese USA Flash Point 192.1ºC
Symbol GHS06 GHS08
GHS06, GHS08		 Signal Word Danger

 Use of Tolterodine tartrate


Tolterodine Tartrate(PNU-200583E; Kabi-2234) is a potent muscarinic receptor antagonists that show selectivity for the urinary bladder over salivary glands in vivo. IC50 Value:Target: mAChRin vitro: Carbachol-induced contractions of isolated guinea pig bladder were effectively inhibited by tolterodine (IC50 14 nM) and 5-HM (IC50 5.7 nM). The IC50 values were in the microM range and the antimuscarinic potency of tolterodine was 27, 200 and 370-485 times higher, respectively, than its potency in blocking histamine receptors, alpha-adrenoceptors and calcium channels. The active metabolite, 5-HM, was >900 times less potent at these sites than at bladder muscarinic receptors [1].in vivo: Tolterodine was extensively metabolized in vivo [2]. In the passive-avoidance test, tolterodine at 1 or 3 mg/kg had no effect on memory; the latency to cross and percentage of animals crossing were comparable to controls. In contrast, scopolamine induced a memory deficit; the latency to cross was decreased, and the number of animals crossing was increased [3].

 Names

Name tolterodine tartrate
Synonym More Synonyms

 Tolterodine tartrate Biological Activity

Description Tolterodine Tartrate(PNU-200583E; Kabi-2234) is a potent muscarinic receptor antagonists that show selectivity for the urinary bladder over salivary glands in vivo. IC50 Value:Target: mAChRin vitro: Carbachol-induced contractions of isolated guinea pig bladder were effectively inhibited by tolterodine (IC50 14 nM) and 5-HM (IC50 5.7 nM). The IC50 values were in the microM range and the antimuscarinic potency of tolterodine was 27, 200 and 370-485 times higher, respectively, than its potency in blocking histamine receptors, alpha-adrenoceptors and calcium channels. The active metabolite, 5-HM, was >900 times less potent at these sites than at bladder muscarinic receptors [1].in vivo: Tolterodine was extensively metabolized in vivo [2]. In the passive-avoidance test, tolterodine at 1 or 3 mg/kg had no effect on memory; the latency to cross and percentage of animals crossing were comparable to controls. In contrast, scopolamine induced a memory deficit; the latency to cross was decreased, and the number of animals crossing was increased [3].
Related Catalog
References

[1]. Nilvebrant L. Tolterodine and its active 5-hydroxymethyl metabolite: pure muscarinic receptor antagonists. Pharmacol Toxicol. 2002 May;90(5):260-7.

[2]. Andersson SH, et al. Biotransformation of tolterodine, a new muscarinic receptor antagonist, in mice, rats, and dogs. Drug Metab Dispos. 1998 Jun;26(6):528-35.

[3]. Cappon GD, et al. Tolterodine does not affect memory assessed by passive-avoidance response test in mice. Eur J Pharmacol. 2008 Jan 28;579(1-3):225-8.

 Chemical & Physical Properties

Density 1.003 g/cm3
Boiling Point 442.2ºC at 760 mmHg
Melting Point 205-210ºC
Molecular Formula C26H37NO7
Molecular Weight 475.574
Flash Point 192.1ºC
Exact Mass 475.256989
PSA 138.53000
LogP 3.21880
Vapour Pressure 1.97E-08mmHg at 25°C
InChIKey TWHNMSJGYKMTRB-KXYUELECSA-N
SMILES Cc1ccc(O)c(C(CCN(C(C)C)C(C)C)c2ccccc2)c1.O=C(O)C(O)C(O)C(=O)O
Storage condition Store at +4°C

 Safety Information

Symbol GHS06 GHS08
GHS06, GHS08
Signal Word Danger
Hazard Statements H301-H361
Precautionary Statements Missing Phrase - N15.00950417-P280
Hazard Codes Xi: Irritant;
Risk Phrases R20/21/22
Safety Phrases S36/37
RIDADR NONH for all modes of transport
HS Code 2922299090

 Synthetic Route

 Customs

HS Code 2922299090
Summary 2922299090. other amino-naphthols and other amino-phenols, other than those containing more than one kind of oxygen function, their ethers and esters; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

 Synonyms

(R)-2-(3-(DIISOPROPYLAMINO)-1-PHENYLPROPYL)-4-METHYLPHENOL 2,3-DIHYDROXYSUCCINATE
(R)-2-(3-DIISOPROPYLAMINO-1-PHENYL-PROPYL)-4-METHYL-PHENOL L-TARTRATE
2-[(1R)-3-(dipropan-2-ylamino)-1-phenylpropyl]-4-methylphenol 2,3-dihydroxybutanedioate (1:1)
MFCD07771985
(R)-2-(3-(Diisopropylamino)-1-phenylpropyl)-4-methylphenol (2R,3R)-2,3-dihydroxysuccinate
(+/-)-TOLTERODINE-D14 TARTRATE
TOLTERODINE
(+)-R)-2-{ALPHA-[2-(DIISOPROPYLAMINO)ETHYL]BENZYL}-P-CRESOL TARTRATE
(+)-R)-2-{A-[2-(DIISOPROPYLAMINO)ETHYL]BENZYL}-P-CRESOL TARTRATE
RIFABUTENE
Tolterodine L-Tartrate
TOLERODINE TARTRATE
Tolterodine tartrate
Butanedioic acid, 2,3-dihydroxy-, (2R,3R)-, compd. with 2-[(1R)-3-[bis(1-methylethyl)amino]-1-phenylpropyl]-4-methylphenol (1:1)
TOLTERODINE TARTRATE, CERTIFIED REFERENCE MATERIAL
(2R,3R)-2,3-Dihydroxysuccinic acid - 2-[(1R)-3-(diisopropylamino)-1-phenylpropyl]-4-methylphenol (1:1)
(R)-2-(3-Diisopropylamino-1-phenyl-propyl)-p-cresol L-tartrate
Tolterodine (Tartrate)
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