1. Metabolic Enzyme/Protease
  2. Endogenous Metabolite
  3. Methoxyacetic acid

Methoxyacetic acid is a metabolite of ethylene glycol monomethyl ether. When the concentration of methoxyacetic acid reaches a certain level, it can inhibit the respiratory function of hepatic mitochondria and testicular mitochondria. Methoxyacetic acid is somewhat toxic.

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Methoxyacetic acid Chemical Structure

Methoxyacetic acid Chemical Structure

CAS No. : 625-45-6

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Liquid + Solvent (Highly Recommended)
10 mM * 1 mL in DMSO
ready for reconstitution
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Based on 1 publication(s) in Google Scholar

Other Forms of Methoxyacetic acid:

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Description

Methoxyacetic acid is a metabolite of ethylene glycol monomethyl ether. When the concentration of methoxyacetic acid reaches a certain level, it can inhibit the respiratory function of hepatic mitochondria and testicular mitochondria. Methoxyacetic acid is somewhat toxic[1][2].

In Vitro

Methoxyacetic acid (>5 mM) inhibits the state 3 succinate oxidation rate and the respiratory control ratio in hepatic mitochondria[1].
Methoxyacetic acid (>3 mM) inhibits the ascorbate/TMPD oxidation rate in testicular mitochondria[1].

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

In Vivo

Methoxyacetic acid (30-300 mg/kg; oral gavage; 8 times, dosed over 10 days) is somewhat toxic to male Fischer 344 rats[2].

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

Animal Model: Male Fischer 344 rats (6-8 weeks of age)[2]
Dosage: 30, 100 and 300 mg/kg
Administration: Oral gavage (i.g.); 5 consecutive days of the first week followed by 3 more consecutive daily doses after a weekend interruption.
Result: Led to a significant decrease in body weight compared to the control group. It also caused severe degeneration of testicular germinal epithelium, a marked reduction in the size of the thymus with depletion of thymic cortical lymphoid elements, and a reduction in bone marrow cellularity, resulting in lower red blood cell counts, hemoglobin concentration, packed cell volume, and white blood cell counts at dose of 300 mg/kg.
Had some similar but less pronounced effects, such as a significant decrease in the relative thymus weight and slight degenerative changes in testicular germinal epithelium in some rats at dose of 100 mg/kg.
Produced no apparent effects during the course of the study at dose of 30 mg/kg.
Molecular Weight

90.08

Formula

C3H6O3

CAS No.
Appearance

Liquid (Density: 1.174 g/cm3)

Color

Colorless to light yellow

SMILES

O=C(O)COC

Structure Classification
Initial Source
Shipping

Room temperature in continental US; may vary elsewhere.

Storage
Pure form -20°C 3 years
4°C 2 years
In solvent -80°C 6 months
-20°C 1 month
Solvent & Solubility
In Vitro: 

DMSO : 100 mg/mL (1110.12 mM; Need ultrasonic; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO)

H2O : 100 mg/mL (1110.12 mM; Need ultrasonic)

Preparing
Stock Solutions
Concentration Solvent Mass 1 mg 5 mg 10 mg
1 mM 11.1012 mL 55.5062 mL 111.0124 mL
5 mM 2.2202 mL 11.1012 mL 22.2025 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, 6 months; -20°C, 1 month. When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.

* 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
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Concentration
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Volume
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Molecular Weight *

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

This equation is commonly abbreviated as: C1V1 = C2V2

Concentration (start)

C1

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Volume (start)

V1

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Concentration (final)

C2

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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: ≥ 2.5 mg/mL (27.75 mM); Clear solution

    This protocol yields a clear solution of ≥ 2.5 mg/mL (saturation unknown).

    Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (25.0 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: ≥ 2.5 mg/mL (27.75 mM); Clear solution

    This protocol yields a clear solution of ≥ 2.5 mg/mL (saturation unknown).

    Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (25.0 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.
Calculation results:
Working solution concentration: mg/mL
This product has good water solubility, please refer to the measured solubility data in water/PBS/Saline for details.
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).
Purity & Documentation

Purity: 99.64%

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, 6 months; -20°C, 1 month. When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.

Optional Solvent Concentration Solvent Mass 1 mg 5 mg 10 mg 25 mg
DMSO / H2O 1 mM 11.1012 mL 55.5062 mL 111.0124 mL 277.5311 mL
5 mM 2.2202 mL 11.1012 mL 22.2025 mL 55.5062 mL
10 mM 1.1101 mL 5.5506 mL 11.1012 mL 27.7531 mL
15 mM 0.7401 mL 3.7004 mL 7.4008 mL 18.5021 mL
20 mM 0.5551 mL 2.7753 mL 5.5506 mL 13.8766 mL
25 mM 0.4440 mL 2.2202 mL 4.4405 mL 11.1012 mL
30 mM 0.3700 mL 1.8502 mL 3.7004 mL 9.2510 mL
40 mM 0.2775 mL 1.3877 mL 2.7753 mL 6.9383 mL
50 mM 0.2220 mL 1.1101 mL 2.2202 mL 5.5506 mL
60 mM 0.1850 mL 0.9251 mL 1.8502 mL 4.6255 mL
80 mM 0.1388 mL 0.6938 mL 1.3877 mL 3.4691 mL
100 mM 0.1110 mL 0.5551 mL 1.1101 mL 2.7753 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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Methoxyacetic acid
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HY-Y1009
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