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L-Histidine monohydrocholoride

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Catalog No. TN8219 Copy Product Info
Purity: 99.88%
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L-Histidine monohydrocholoride is the essential amino acid. It is highly water-soluble and is commonly used in cell culture media, buffer systems, and biochemical research. Its imidazole side chain can participate in metal ion binding and acid-base buffering, playing a crucial role in protein structural stability and enzymatic catalysis.
L-Histidine monohydrocholoride
Cas No. 645-35-2
Pack SizePriceUSA StockGlobal StockQuantity
5 g$29-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:99.88%
Appearance:Solid
Color:White
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Product Introduction

Bioactivity
Description
L-Histidine monohydrocholoride is the essential amino acid. It is highly water-soluble and is commonly used in cell culture media, buffer systems, and biochemical research. Its imidazole side chain can participate in metal ion binding and acid-base buffering, playing a crucial role in protein structural stability and enzymatic catalysis.
In vitro
L-Histidine monohydrocholoride significantly reduced air-liquid biofilm formation and adhesion to polystyrene in Flor yeast, but did not affect the transcriptional levels of the FLO11 gene.
L-Histidine monohydrocholoride completely inhibited growth, and its effect on survival was inversely proportional to FLO11 expression.
L-Histidine monohydrocholoride did not affect the survival of the Δflo11 and S288c strains.
L-Histidine monohydrocholoride also altered the content of chitin and polysaccharides in the cell walls of Flor yeast.
In vivo
L-Histidine monohydrocholoride (100 mg/kg) completely inhibited cerebral edema in rats treated with thioacetamide.
In the L-Histidine monohydrocholoride diet group, histamine release in hypothalamic tissue induced by high potassium ions was only 60% of that in the control group; no significant changes were observed in the concentrations of other monoamines and their metabolites.
The open field test indicated that the L-Histidine monohydrocholoride-fed group spent less time in the central area.
In the light/dark box test, the L-Histidine monohydrocholoride-fed group also spent less time in the light compartment, suggesting that the L-Histidine monohydrocholoride diet may induce anxiety-like behavior.
Chemical Properties
Molecular Weight191.62
FormulaC6H10ClN3O2
Cas No.645-35-2
SmilesC([C@@H](C(O)=O)N)C1=CN=CN1.Cl
SequenceH-His-OH
Sequence ShortH
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
DMSO: 40 mg/mL (208.75 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM5.2187 mL26.0933 mL52.1866 mL260.9331 mL
5 mM1.0437 mL5.2187 mL10.4373 mL52.1866 mL
10 mM0.5219 mL2.6093 mL5.2187 mL26.0933 mL
20 mM0.2609 mL1.3047 mL2.6093 mL13.0467 mL
50 mM0.1044 mL0.5219 mL1.0437 mL5.2187 mL
100 mM0.0522 mL0.2609 mL0.5219 mL2.6093 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

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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: L-Histidine monohydrocholoride chemical structure | L-Histidine monohydrocholoride in vivo | L-Histidine monohydrocholoride in vitro | L-Histidine monohydrocholoride formula | L-Histidine monohydrocholoride molecular weight