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Cat. No.: HY-78086R

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m-Tolualdehyde (Standard)

(Synonyms: 3-Methylbenzaldehyde (Standard))

m-Tolualdehyde (Standard) is the analytical standard of m-Tolualdehyde (HY-78086). This product is intended for research and analytical applications. m-Tolualdehyde (3-Methylbenzaldehyde) is an aldehyde metabolite produced by m-xylene metabolism, and it bidirectionally regulates the CYP 2B1, CYP 2E1, and CYP 4B1 isoenzymes in the respiratory tract of rats. m-Tolualdehyde serves as an oxidation substrate and carbon source for Pseudomonas Pxy, and it can be oxidized to m-toluic acid in an NAD⁺-dependent manner. m-Tolualdehyde exerts a dose-dependent inhibitory effect on CYP 2B1 and CYP 2E1 in the nasal mucosa and lungs of rats, and a dose-dependent activating effect on pulmonary CYP 4B1. m-Tolualdehyde can form aldehyde-heme adducts with the heme group of cytochrome P450. m-Tolualdehyde can be used in studies related to metabolic enzymes in the respiratory tract of rats.

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

CAS No.: 620-23-5
Formula: C₈H₈O
Molecular Weight:120.15

Storage:

Please store the product under the recommended conditions in the Certificate of Analysis.

m-Tolualdehyde (Standard) Chemical Structure

CAS No.: 620-23-5

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Product Information
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- Application
Chemical Information
Purity & Documentation
Calculators
Help & FAQs
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Product Information

Information

Application

The compound is the grade of analytical standard, which is the reference standard supplied assay. It is commonly used in qualitative, quantitative and methodological research experiments in HPLC, GC and MS.

Chemical Information

CAS No. 620-23-5
Molecular Weight 120.15
Formula C₈H₈O
SMILES

O=CC1=CC=CC(C)=C1
Synonyms

3-Methylbenzaldehyde (Standard)
Structure Classification
- Ketones, Aldehydes, Acids
Initial Source
- Plants
- Labiatae
Shipping

Room temperature in continental US; may vary elsewhere.
Storage

Please store the product under the recommended conditions in the Certificate of Analysis.

Purity & Documentation

Select Batch:

Purity: 99.98%

Assay: 99.98%

ee.: 99.98%

References

[1]. Vaidyanathan A, et al.. Inhibition of rat respiratory-tract cytochrome P-450 isozymes following inhalation of m-Xylene: possible role of metabolites. Journal of toxicology and environmental health. Part A. 2003 Jun 27;66(12):1133-43. [Content Brief]

[2]. Davey JF, et al.. Bacterial metabolism of para- and meta-xylene: oxidation of a methyl substituent. Journal of bacteriology. 1974 Sep;119(3):923-9. [Content Brief]

Calculators

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Help & FAQs

How should lyophilized recombinant proteins be reconstituted and stored?

1. Before opening the cap, centrifuge the vial at 13000 rpm for 20-30 seconds. This step will ensure that any lyophilized powder that may have adhered to the cap or walls is collected at the bottom of the vial, minimizing the risk of product loss.

100 mg

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