Dimetindene maleate - CAS 3614-69-5
Catalog number: B0084-343416
Category: Inhibitor
Please be kindly noted products are not for therapeutic use. We do not sell to patients.
Molecular Formula:
C24H28N2O4
Molecular Weight:
408.498
COA:
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Targets:
Histamine Receptor
Description:
Dimethindene is a histamine H1 antagonist of high potency used orally and locally as an antipruritic.
Ordering Information
Catalog Number Size Price Stock Quantity
B0084-343416 25 mg $299 In stock
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Brife Description:
histamine H1 antagonist
Purity:
≥98%
Appearance:
White solid
Synonyms:
Fenistil-retard; Forhistal maleate; U 6518; SU-6518; UNII-6LL60J9E0O; Dimethindene maleate; Dimethpyrindene maleate;Dimetindene maleate; EINECS 222-789-2; Fenistil; Fenistil-retard; Forhistal maleate; NSC 107677; N,N-Dimethyl-3-[1-(2-pyridinyl)ethyl]-1H-indene-2-ethanamine maleate; (Z)-but-2-enedioic acid; N,N-dimethyl-2-[3-(1-pyridin-2-ylethyl)-1H-inden-2-yl]ethanamine
Solubility:
Soluble in DMSO
Storage:
Store at -20 °C
MSDS:
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Application:
antipruritic
Shelf Life:
As supplied, 2 years from the QC date provided on the Certificate of Analysis, when stored properly.
Boiling Point:
416.3ºC at 760mmHg
InChIKey:
SWECWXGUJQLXJF-BTJKTKAUSA-N
InChI:
InChI=1S/C20H24N2.C4H4O4/c1-15(19-10-6-7-12-21-19)20-17(11-13-22(2)3)14-16-8-4-5-9-18(16)20;5-3(6)1-2-4(7)8/h4-10,12,15H,11,13-14H2,1-3H3;1-2H,(H,5,6)(H,7,8)/b;2-1-
Canonical SMILES:
CC(C1=CC=CC=N1)C2=C(CC3=CC=CC=C32)CCN(C)C.C(=CC(=O)O)C(=O)O
1.Prevention of postoperative adhesion formation by individual and combined administration of 4 per cent icodextrin and dimetindene maleate (Br J Surg 2009; 96: 1476-1483).
Watkins PE. Br J Surg. 2010 Mar;97(3):459; author reply 459. doi: 10.1002/bjs.7015.
2.Application of HILIC stationary phase to determination of dimethindene maleate in topical gel.
Matysová L1, Havlíková L, Hájková R, Krivda A, Solich P. J Pharm Biomed Anal. 2009 Aug 15;50(1):23-6. doi: 10.1016/j.jpba.2009.03.032. Epub 2009 Apr 5.
A novel high performance liquid chromatography method for the determination of dimethindene maleate in pharmaceutical gel using hydrophilic interaction liquid chromatography (HILIC) with UV detection was developed and validated. Following optimal conditions for the analysis of dimethindene maleate were used: analytical column SeQuant ZIC-HILIC (50mmx2.1mm, 5microm), and mobile phase consisted of a mixture of acetonitrile and aqueous solution of acetic acid (25mM) and ammonium acetate (2.5mM) (87.5:12.5, v:v). The analysis time was less than 3min at a flow rate of 0.3mlmin(-1). UV detection was performed at 258nm. The method was validated and system suitability parameters were evaluated. The method is suitable for application for routine determination of dimethindene maleate in topical pharmaceutical preparation.
3.Contact dermatitis and secondary systemic allergy to dimethindene maleate.
Leroy A1, Baeck M, Tennstedt D. Contact Dermatitis. 2011 Mar;64(3):170-1. doi: 10.1111/j.1600-0536.2010.01830.x.
4.Identification and determination of ketotifen hydrogen fumarate, azelastine hydrochloride, dimetindene maleate and promethazine hydrochloride by densitometric method.
Wyszomirska E1, Czerwińska K2, Kublin E2, Mazurek AP2. Acta Pol Pharm. 2013 Nov-Dec;70(6):951-9.
Conditions for determination of: ketotifen hydrogen fumarate, azelastine hydrochloride, dimetindene maleate and promethazine hydrochloride by densitometric method in substances and pharmaceuticals were provided. Maximum wavelenghts were: 228 nm for ketotifen hydrogen fumarate, 295 nm for azelastine hydrochloride, 265 nm for dimetindene maleate and 255 nm for promethazine hydrochloride. The limits of quantification were in the ranges of 0.2-5 microg/spot. The statistical data showed adequate accuracy and precision of developed methods.
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CAS 3614-69-5 Dimetindene maleate

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