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  3. Riboflavin

Riboflavin  (Synonyms: Vitamin B2; E101)

Cat. No.: HY-B0456 Purity: 99.55%
COA Handling Instructions

Riboflavin, an orally active and easily absorbed micronutrient, is a precursor of flavin mononucleotide (FMN) and flavin adenine dinucleotide (FAD), which serve as coenzymes for numerous enzymatic reactions and perform key metabolic functions by mediating the transfer of electrons in biological oxidation-reduction reaction.

For research use only. We do not sell to patients.

Riboflavin Chemical Structure

Riboflavin Chemical Structure

CAS No. : 83-88-5

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10 mM * 1 mL in DMSO
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Customer Review

Based on 1 publication(s) in Google Scholar

Other Forms of Riboflavin:

Top Publications Citing Use of Products
  • Biological Activity

  • Purity & Documentation

  • References

  • Customer Review

Description

Riboflavin, an orally active and easily absorbed micronutrient, is a precursor of flavin mononucleotide (FMN) and flavin adenine dinucleotide (FAD), which serve as coenzymes for numerous enzymatic reactions and perform key metabolic functions by mediating the transfer of electrons in biological oxidation-reduction reaction[1].

IC50 & Target

Human Endogenous Metabolite

 

Microbial Metabolite

 

In Vitro

Riboflavin (5-50 µM, 24 h) has a strong cytotoxic effect on HL60 cells after UV irradiation that is mediated by apoptosis[2].
Riboflavin (0.76-48.76 nM, 96 h) increases cell viability and glutathione reductase activity and reduces apoptosis of HepG2 cells in a dose-dependent manner[3].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Cell Viability Assay[2]

Cell Line: HL60 cells
Concentration: 5-10 µM
Incubation Time: 24 h
Result: Didn't affect cell viability with no UV irradiation.

Western Blot Analysis[2]

Cell Line: HL60 cells
Concentration: 5-50 µM
Incubation Time: 24 h
Result: Increased the ratio Bax/Bcl2 and decreased the level of inhibitory apoptosis protein type 1 (IAP1).
Caused overexpression of Fas and FasL.
Decreased the expression of TNFR1 and TRADD at the concentration of 10-50 µM.
Inhibited the cell survival relevant kinases phospho-JNK, phospho-MEK, phospho-ERK.
Increased the expression of p21 and decreased the expression of PCNA, STATs 1 and STATs 2.
In Vivo

Riboflavin (10 mg/kg, p.o., daily) promotes the growth of swiss albino mice[4].
Riboflavin (1-600 mg/kg, p.o., one time) produces antinociceptive, antihyperalgesic, and anti-inflammatory effect in formalin, carrageenan-induced thermal hyperalgesia, and spinal nerve ligation rat models[5].
Riboflavin (3-100 mg/kg, i.p., one time) inhibits the nociceptive response in a dose-dependent manner in mice model of acetic acid-induced constriction[6].
Riboflavin (6-12 mg/kg, i.p., one time) decreases the second phase nociceptive response in mice model of formaldehyde-induced[6].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: Swiss albino mice[4]
Dosage: 10 mg/kg
Administration: Oral gavage (p.o.), daily
Result: Increased the growth rate of pregnant and newbron mice.
Increased the percent conception and average litter size of pregnant mices.
Improved the percent zinc absorption in male mices.
Increased the levels of zinc and iron in organs in male and female mices.
Increased the percent hemoglobin and the blood zinc value of female mices.
Animal Model: Female Wistar rats[5]
Dosage: 1-600 mg/kg
Administration: Oral gavage (p.o.), one time
Result: Reduced flinching behavior during phase 2 in formalin-injected mice by doses of 1-50 mg/kg.
Produced a significant antihyperalgesic effect in carrageenan-injected mice by doses of 6.25-150 mg/kg.
Reduced carrageenan-induced edema by doses of 50-150 mg/kg.
Didn’t reduce tactile allodynia in the spinal nerve ligation model by doses of 150-600 mg/kg.
Clinical Trial
Molecular Weight

376.36

Formula

C17H20N4O6

CAS No.
Appearance

Solid

Color

Yellow to orange

SMILES

O[C@H]([C@H](O)[C@H](O)CO)CN1C(C=C(C)C(C)=C2)=C2N=C(C(N3)=O)C1=NC3=O

Structure Classification
Initial Source
Shipping

Room temperature in continental US; may vary elsewhere.

Storage

4°C, protect from light

*In solvent : -80°C, 1 year; -20°C, 6 months (protect from light)

Solvent & Solubility
In Vitro: 

H2O : 14.29 mg/mL (37.97 mM; ultrasonic and adjust pH to 8 with NaOH)

DMSO : 5.56 mg/mL (14.77 mM; ultrasonic and warming and heat to 60°C; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO)

Preparing
Stock Solutions
Concentration Solvent Mass 1 mg 5 mg 10 mg
1 mM 2.6570 mL 13.2852 mL 26.5703 mL
5 mM 0.5314 mL 2.6570 mL 5.3141 mL
View the Complete Stock Solution Preparation Table

* Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 1 year; -20°C, 6 months (protect from light). When stored at -80°C, please use it within 1 year. When stored at -20°C, please use it within 6 months.

* Note: If you choose water as the stock solution, please dilute it to the working solution, then filter and sterilize it with a 0.22 μm filter before use.

  • Molarity Calculator

  • Dilution Calculator

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

Mass
=
Concentration
×
Volume
×
Molecular Weight *

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

Concentration (start)

C1

×
Volume (start)

V1

=
Concentration (final)

C2

×
Volume (final)

V2

In Vivo:

Select the appropriate dissolution method based on your experimental animal and administration route.

For the following dissolution methods, please ensure to first prepare a clear stock solution using an In Vitro approach and then sequentially add co-solvents:
To ensure reliable experimental results, the clarified stock solution can be appropriately stored based on storage conditions. As for the working solution for in vivo experiments, it is recommended to prepare freshly and use it on the same day.
The percentages shown for the solvents indicate their volumetric ratio in the final prepared solution. If precipitation or phase separation occurs during preparation, heat and/or sonication can be used to aid dissolution.

  • Protocol 1

    Add each solvent one by one:  10% DMSO    40% PEG300    5% Tween-80    45% Saline

    Solubility: ≥ 0.56 mg/mL (1.49 mM); Clear solution

    This protocol yields a clear solution of ≥ 0.56 mg/mL (saturation unknown).

    Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (5.6 mg/mL) to 400 μL PEG300, and mix evenly; then add 50 μL Tween-80 and mix evenly; then add 450 μL Saline to adjust the volume to 1 mL.

    Preparation of Saline: Dissolve 0.9 g sodium chloride in ddH₂O and dilute to 100 mL to obtain a clear Saline solution.
  • Protocol 2

    Add each solvent one by one:  10% DMSO    90% (20% SBE-β-CD in Saline)

    Solubility: ≥ 0.56 mg/mL (1.49 mM); Clear solution

    This protocol yields a clear solution of ≥ 0.56 mg/mL (saturation unknown).

    Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (5.6 mg/mL) to 900 μL 20% SBE-β-CD in Saline, and mix evenly.

    Preparation of 20% SBE-β-CD in Saline (4°C, storage for one week): 2 g SBE-β-CD powder is dissolved in 10 mL Saline, completely dissolve until clear.
In Vivo Dissolution Calculator
Please enter the basic information of animal experiments:

Dosage

mg/kg

Animal weight
(per animal)

g

Dosing volume
(per animal)

μL

Number of animals

Recommended: Prepare an additional quantity of animals to account for potential losses during experiments.
Please enter your animal formula composition:
%
DMSO +
+
%
Tween-80 +
%
Saline
Recommended: Keep the proportion of DMSO in working solution below 2% if your animal is weak.
The co-solvents required include: DMSO, . All of co-solvents are available by MedChemExpress (MCE). , Tween 80. All of co-solvents are available by MedChemExpress (MCE).
Calculation results:
Working solution concentration: mg/mL
Method for preparing stock solution: mg drug dissolved in μL  DMSO (Stock solution concentration: mg/mL).

*In solvent : -80°C, 1 year; -20°C, 6 months (protect from light)

The concentration of the stock solution you require exceeds the measured solubility. The following solution is for reference only. If necessary, please contact MedChemExpress (MCE).
Method for preparing in vivo working solution for animal experiments: Take μL DMSO stock solution, add μL . μL , mix evenly, next add μL Tween 80, mix evenly, then add μL Saline.
 If the continuous dosing period exceeds half a month, please choose this protocol carefully.
Please ensure that the stock solution in the first step is dissolved to a clear state, and add co-solvents in sequence. You can use ultrasonic heating (ultrasonic cleaner, recommended frequency 20-40 kHz), vortexing, etc. to assist dissolution.
Purity & Documentation

Purity: 99.55%

References

Complete Stock Solution Preparation Table

* Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 1 year; -20°C, 6 months (protect from light). When stored at -80°C, please use it within 1 year. When stored at -20°C, please use it within 6 months.

Optional Solvent Concentration Solvent Mass 1 mg 5 mg 10 mg 25 mg
DMSO / H2O 1 mM 2.6570 mL 13.2852 mL 26.5703 mL 66.4258 mL
5 mM 0.5314 mL 2.6570 mL 5.3141 mL 13.2852 mL
10 mM 0.2657 mL 1.3285 mL 2.6570 mL 6.6426 mL
H2O 15 mM 0.1771 mL 0.8857 mL 1.7714 mL 4.4284 mL
20 mM 0.1329 mL 0.6643 mL 1.3285 mL 3.3213 mL
25 mM 0.1063 mL 0.5314 mL 1.0628 mL 2.6570 mL
30 mM 0.0886 mL 0.4428 mL 0.8857 mL 2.2142 mL

* Note: If you choose water as the stock solution, please dilute it to the working solution, then filter and sterilize it with a 0.22 μm filter before use.

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Help & FAQs
  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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