Isovanillin (Standard)
Isovanillin (Standard) is the analytical standard of Isovanillin. This product is intended for research and analytical applications. Isovanillin is an aldehyde oxidase inhibitor. Antispasmodic activities. Antidiarrheal activities.
Para uso exclusivo en investigación. No vendemos a pacientes.
- Pureza : 98%
- No. CAS: 621-59-0
- Fòrmula: C8H8O3
- Peso molecular:152.15
-
Almacenamiento:
Please store the product under the recommended conditions in the Certificate of Analysis.
To place orders, for customer services and technical support, please contact: MedChemExpress USA
Tel: 609-228-6898 E-mail: [email protected] [email protected]
-
Product Information
-
Chemical Information
- Pureza y Documentación
-
Help & FAQs
-
HY-I0637
IsovanillinAldehyde Oxidase Inhibitor -
HY-Y0740
4-MethoxybenzaldehydePhenol -
HY-76006
3-HydroxybenzaldehydeSubstrate For ALDH, Precursor Compound for Phenolic Compounds -
HY-N0098
VanillinPhenolic Aldehyde -
HY-N0295
ProtocatechualdehydePolyphenol Compound -
HY-Y0015
p-DimethylaminobenzaldehydeChromogenic Reagent -
HY-N1390
SyringaldehydeCOX-2 Inhibitor -
HY-Y0313
p-Hydroxybenzaldehyde -
HY-N1096
VeratraldehydeAromatic Compound -
HY-N0098R
Vanillin (Standard) -
HY-W017446
4-Formylbenzoic acidBiochemical Reagent -
HY-Y0313R
p-Hydroxybenzaldehyde (Standard)
Product Information
Information
Aplicación
The compound is the grade of analytical standard, which is the reference standard supplied assay. It is commonly used in qualitative, quantitative and methodological research experiments in HPLC, GC and MS.
Chemical Information
-
No. CAS 621-59-0
-
Appearance Solid
-
Peso molecular 152.15
-
Fòrmula C8H8O3
-
Color White to off-white
-
SMILES
O=CC1=CC=C(OC)C(O)=C1
-
Synonyms
3-Hydroxy-4-methoxybenzaldehyde (Standard)
-
Structure Classification
-
Initial Source
-
Envío
Room temperature in continental US; may vary elsewhere.
-
Almacenamiento
Please store the product under the recommended conditions in the Certificate of Analysis.
Pureza y Documentación
-
SDS (252 KB)
- Français - FR (252 KB)
- Deutsch - DE (252 KB)
- Norwegian - NO (252 KB)
- Español - ES (252 KB)
- Swedish - SV (252 KB)
- Italian - IT (252 KB)
- Korean - KR (252 KB)
- Portuguese - PT (252 KB)
-
Instrucciones de manejo (2659 KB)
Referencias
[1]. Panoutsopoulos GI, et al. Enzymatic oxidation of vanillin, isovanillin and protocatechuic aldehyde with freshly prepared Guinea pig liver slices. Cell Physiol Biochem. 2005;15(1-4):89-98. [Content Brief]
[2]. Sadraei H, et al. Antispasmodic activity of isovanillin and isoacetovanillon in comparison with Pycnocycla spinosa Decne.exBoiss extract on rat ileum. Res Pharm Sci. 2014 May-Jun;9(3):187-92. [Content Brief]
[3]. Sadraei H, et al. Antidiarrheal activities of isovanillin, iso-acetovanillon and Pycnocycla spinosa Decne ex.Boiss extract in mice. Res Pharm Sci. 2014 Mar-Apr;9(2):83-9. [Content Brief]
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
Isovanillin (Standard) Related Classifications
HY-I0637R Related Classifications
Powered by Bioz