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4,6-Dimethoxysalicylaldehyde
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Catalog No. TN9425Cas No. 708-76-9
Alias 2-Hydroxy-4,6-dimethoxybenzaldehyde
4,6-Dimethoxysalicylaldehyde inhibits hepatic gluconeogenesis in rat hepatocellular carcinoma cells H4-II-E-C3, which can be used to study type 2 diabetes.
4,6-Dimethoxysalicylaldehyde
😃Good
Purity: 99.81%
Catalog No. TN9425Alias 2-Hydroxy-4,6-dimethoxybenzaldehydeCas No. 708-76-9
4,6-Dimethoxysalicylaldehyde inhibits hepatic gluconeogenesis in rat hepatocellular carcinoma cells H4-II-E-C3, which can be used to study type 2 diabetes.
| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 50 mg | $35 | - | In Stock | |
| 100 mg | $50 | - | In Stock |
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
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Purity:99.81%
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Product Introduction
Bioactivity
Chemical Properties
| Description | 4,6-Dimethoxysalicylaldehyde inhibits hepatic gluconeogenesis in rat hepatocellular carcinoma cells H4-II-E-C3, which can be used to study type 2 diabetes. |
| In vitro | 4,6-Dimethoxysalicylaldehyde exhibits in vitro antibacterial activity against Campylobacter jejuni with a BA₅₀ value of 0.038[1]. |
| Synonyms | 2-Hydroxy-4,6-dimethoxybenzaldehyde |
| Molecular Weight | 182.17 |
| Formula | C9H10O4 |
| Cas No. | 708-76-9 |
| Smiles | O=CC=1C(O)=CC(OC)=CC1OC |
Storage & Solubility Information
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. |
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(mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.Preparation method for in vivo formula: Take 50 μL DMSO main solution, add 300 μLPEG300 mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLSaline/PBS/ddH2O mix well and clarify
main solution, add 300 μLPEG300 mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLSaline/PBS/ddH2O mix well and clarifyFor Reference Only. Please develop an appropriate dissolution method based on your laboratory animals and route of administration.
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