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Key Documents

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B5524

Supelco

Benzydamine hydrochloride

analytical standard

Sinónimos:

1-Benzyl-3-(3-[dimethylamino]propoxy)-1H-indazole

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About This Item

Fórmula empírica (notación de Hill):
C19H23N3O · HCl
Número de CAS:
132-69-4
Peso molecular:
345.87
EC Number:
205-076-0
MDL number:
MFCD00078957
UNSPSC Code:
41116107
PubChem Substance ID:
329773263
NACRES:
NA.24

grade

analytical standard

Quality Level

200

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

forensics and toxicology
pharmaceutical (small molecule)
veterinary

format

neat

storage temp.

2-8°C

SMILES string

Cl.CN(C)CCCOc1nn(Cc2ccccc2)c3ccccc13

InChI

1S/C19H23N3O.ClH/c1-21(2)13-8-14-23-19-17-11-6-7-12-18(17)22(20-19)15-16-9-4-3-5-10-16;/h3-7,9-12H,8,13-15H2,1-2H3;1H

InChI key

HNNIWKQLJSNAEQ-UHFFFAOYSA-N

Gene Information

human ... PTGS1(5742) , PTGS2(5743)

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Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

pictograms

Exclamation mark
GHS07

signalword

Warning

hcodes

H302,H319

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

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Certificados de análisis (COA)

Lot/Batch Number
0000257025
0000254328
035K0816
124K1460
114K1229

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N R Patil et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 79(5), 1985-1991 (2011-07-01)
Fluorescence quenching of biologically active carboxamide namely (E)-2-(4-chlorobenzylideneamino)-N-(2-chlorophenyl)-4,5,6,7-tetrahydrobenzo[b]thiophene-3-carboxamide [ECNCTTC] by aniline and carbon tetrachloride (CCl4) quenchers in different solvents using steady state method and time resolved method using only one solvent has been carried out at room temperature to understand
S Y Karavana Hizarcioğlu et al.
International journal of oral and maxillofacial surgery, 40(9), 973-978 (2011-05-10)
The aim of this study was to investigate the effect of benzydamine hydrochloride bioadhesive gel on healing of oral mucosal ulceration in an animal model. For in vivo determination of the effects of the bioadhesive gel, 36 rabbits were separated
Yadira X Perez-Paramo et al.
Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 28(2), 311-320 (2018-11-02)
The major mode of metabolism of nicotine is by hydroxylation via cytochrome P450 (CYP) 2A6, but it can also undergo glucuronidation by UDP-glucuronosyltransferases and oxidation by flavin monooxygenases (FMO). The goal of this study was to examine the potential importance
Ali Fuat Erciyas et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 48(10), 2577-2580 (2010-07-06)
In this study, genotoxicity of two mouthwash products (chlorexidin, benzidamine-HCl) were investigated in the Drosophila Wing-Spot Test which makes use of the wing cell markers multiple wing hairs (mwh) and flare (flr) and detects both mitotic recombination and various types
Koray Soygun et al.
The journal of advanced prosthodontics, 9(3), 200-207 (2017-07-07)
In this study, three bioceramic materials, [IPS Empress CAD (Ivoclar), IPS e.max CAD (Ivoclar), and Lava Ultimate CAD (3M ESPE)] were treated with three commercial mouthrinses [Listerine, Tantum Verde, and Klorhex]; and changes in colour reflectance and surface roughness values
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