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Saccharic acid

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Catalog No. T201826 Copy Product Info
Purity: 99.89%
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Saccharic acid (also known as glucaric acid) is a dicarboxylic acid formed by the oxidation of glucose, and it is an important intermediate in the study of sugar metabolism and carbohydrate oxidation. It acts as a competitive inhibitor of β-glucuronidase, preventing the hydrolysis of glucuronides that have already bound to toxins, thereby blocking the regeneration of toxic complexes.
Saccharic acid
Cas No. 87-73-0
Pack SizePriceUSA StockGlobal StockQuantity
50 mg$31-In Stock
100 mg$52-In Stock
For In stock only · Estimated delivery: USA Stock (1-2 days) Global Stock (5-7 days)
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For research use only—not for human use. No sales to individuals. Use as intended only.
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Purity:99.89%
Appearance:Solid
Color:White
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Product Introduction

Bioactivity
Description
Saccharic acid (also known as glucaric acid) is a dicarboxylic acid formed by the oxidation of glucose, and it is an important intermediate in the study of sugar metabolism and carbohydrate oxidation. It acts as a competitive inhibitor of β-glucuronidase, preventing the hydrolysis of glucuronides that have already bound to toxins, thereby blocking the regeneration of toxic complexes.
In vitro
Saccharic acid (50 µM Fe(III)-saccharic acid + 90 min UV-C irradiation) enhances the photofenton degradation of methylene blue [1].
Saccharic acid (50–150 × 10^(−4) M; 1 h) potently, competitively, and reversibly inhibits β-glucuronidase activity in mouse liver and kidney [2].
Saccharic acid (1 × 10^(−3) M; 2 h) strongly inhibits the hydrolysis of o-aminophenyl-glucuronide by mouse liver β-glucuronidase preparations [2].
Saccharic acid (0.01 M; 90 min) reduces β-glucuronidase activity in intact mouse liver sections [2].
In vivo
Saccharic acid (5 g/kg; subcutaneous injection; administered daily; continued until day 8) does not alter the liver regeneration process following carbon tetrachloride-induced injury or partial hepatectomy [2].
Saccharic acid (2 g/kg; intraperitoneal injection; daily; 3 weeks) or (3%; dietary supplementation; ad libitum; 3 weeks) does not alter normal growth in young mice [2].
Chemical Properties
Molecular Weight210.139
FormulaC6H10O8
Cas No.87-73-0
SmilesOC([C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C(O)=O)=O
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year Shipping with blue ice/Shipping at ambient temperature.
Solubility Information
H2O: 200.00 mg/mL (951.75 mM), Sonication is recommended.
Solution Preparation Table
H2O
1mg5mg10mg50mg
1 mM4.7588 mL23.7938 mL47.5875 mL237.9377 mL
5 mM0.9518 mL4.7588 mL9.5175 mL47.5875 mL
10 mM0.4759 mL2.3794 mL4.7588 mL23.7938 mL
20 mM0.2379 mL1.1897 mL2.3794 mL11.8969 mL
50 mM0.0952 mL0.4759 mL0.9518 mL4.7588 mL
100 mM0.0476 mL0.2379 mL0.4759 mL2.3794 mL
Note : The dilution table applies only to solid products. For liquid products, please calculate the stock solution based on the stated concentration and/or density.

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In Vivo Formulation Calculator (Clear solution)

Please enter your animal experiment information in the following box and click Calculate to obtain the stock solution preparation method and in vivo formula preparation method:
TargetMol | Animal experiments For example, if the intended dosage is 10 mg/kg for animals weighing 20 g , with a dosing volume of 100 μL per animal, TargetMol | Animal experiments and a total of 10 animals are to be administered, using a formulation of TargetMol | reagent 10% DMSO+ 40% PEG300+ 5% Tween 80+ 45% Saline/PBS/ddH2O , the resulting working solution concentration would be 2 mg/mL.
Stock Solution Preparation:

Dissolve 2 mg of the compound in 100 μL DMSOTargetMol | reagent to obtain a stock solution at a concentration of 20 mg/mL . If the required concentration exceeds the compound's known solubility, please contact us for technical support before proceeding.

Preparation of the In Vivo Formulation:

1) Add 100 μL of the DMSOTargetMol | reagent stock solution to 400 µL PEG300TargetMol | reagent and mix thoroughly until the solution becomes clear.

2) Add 50 µL Tween 80 and mix well until fully clarified.

3) Add 450 µL Saline,PBS or ddH2OTargetMol | reagent and mix thoroughly until a homogeneous solution is obtained.

This example is provided solely to demonstrate the use of the In Vivo Formulation Calculator and does not constitute a recommended formulation for any specific compound. Please select an appropriate dissolution and formulation strategy based on your experimental model and route of administration.
All co-solvents required for this protocol, includingDMSO, PEG300/PEG400, Tween 80, SBE-β-CD, and Corn oil, are available for purchase on the TargetMol website.
1 Enter information below:
mg/kg
g
µL
2 Enter the in vivo formulation:
% DMSO
%
% Tween 80
% Saline/PBS/ddH2O

Dose Conversion

You can also refer to dose conversion for different animals. More Dose Conversion

Tech Support

Please see Inhibitor Handling Instructions for more frequently ask questions. Topics include: how to prepare stock solutions, how to store products, and cautions on cell-based assays & animal experiments, etc
Related Tags: Saccharic acid chemical structure | Saccharic acid in vivo | Saccharic acid in vitro | Saccharic acid formula | Saccharic acid molecular weight