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109622

Sigma-Aldrich

2-Methoxybenzaldehyde

98%

Synonym(s):

o-Anisaldehyde, Salicylaldehyde methyl ether

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¥2,650
100 G
¥7,410
500 G
¥22,900

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Estimated to ship onApril 11, 2025

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2 G
¥2,650
100 G
¥7,410
500 G
¥22,900

About This Item

Linear Formula:
CH3OC6H4CHO
CAS Number:
135-02-4
Molecular Weight:
136.15
Beilstein:
606301
EC Number:
205-171-7
MDL number:
MFCD00003308
UNSPSC Code:
12352100
PubChem Substance ID:
24846928
NACRES:
NA.22

¥2,650

Estimated to ship onApril 11, 2025

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Quality Level

100

Assay

98%

form

solid

bp

238 °C (lit.)

mp

34-40 °C (lit.)

density

1.127 g/mL at 25 °C (lit.)

functional group

aldehyde

SMILES string

[H]C(=O)c1ccccc1OC

InChI

1S/C8H8O2/c1-10-8-5-3-2-4-7(8)6-9/h2-6H,1H3

InChI key

PKZJLOCLABXVMC-UHFFFAOYSA-N

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General description

2-Methoxybenzaldehyde is used as a starting material to synthesize corrosion-inhibiting Schiff bases. Also used as a flavor and fragrance ingredient. [1]

Application

2-Methoxybenzaldehyde has been used to examine the acaricidal activity of Periploca sepium oil and its active component against Tyrophagus putrescentiae[2].
2-Methoxybenzaldehyde has been used to obtain good enantioselectivities using Cu(OAc)(2)-bis(oxazolines) via hydrogen bonding in asymmetric Henry reaction[3].

Biochem/physiol Actions

Naturally-occurring aromatic aldehyde with acaricidal activity. May condense with L-tryptophan in foods to form the corresponding phenolic tetrahydro-β-carboline-3-carboxylic acid which is a potent antioxidant.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 2

Flash Point(F)

244.4 °F - closed cup

Flash Point(C)

118 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

109622-500G:
109622-100G:
109622-VAR:
109622-2G:
109622-BULK:

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Certificates of Analysis (COA)

Lot/Batch Number
WXBF2609V
WXBF0541V
STBK6969
STBK5276
STBK0322

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Synthesis, experimental and computational studies on the anti-corrosion performance of substituted Schiff bases of 2-methoxybenzaldehyde for mild steel in HCl medium
Collins I U et al.
Scientific Reports, 13, 3265-3265 (2023)
Eun-Young Jeong et al.
Journal of food protection, 75(1), 118-122 (2012-01-10)
The aim of this study was to examine the acaricidal activity of Periploca sepium oil and its active component against Tyrophagus putrescentiae. Based on its 50% lethal dose (LD(50) ) value, P. sepium oil (8.45 μg/cm(2)) was highly active against
Ninghua Yin et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 153, 1-5 (2015-08-19)
A facile fluorescence switch with Schiff base units was designed and achieved by nucleophilic addition and dehydration reaction. The fluorescence of the probe can be regulated by metal ions (Al(3+) and Cu(2+)). The whole process shows that the weak fluorescence
Olga V Kupriyanova et al.
Drug testing and analysis, 12(8), 1154-1170 (2020-05-18)
N-(2-Methoxybenzyl)-2,5-dimethoxyphenethylamines (NBOMes) are synthetic phenethylamine derivatives emerging on the global drug market and reported to be associated with untoward effects in people who use drugs. Its action involves agonism at serotonin 5-HT2A receptors, affecting cognitive and behavioral processes. However, certain
Zhi-Huai Li et al.
Chirality, 24(12), 1092-1095 (2012-09-25)
Immobilized Cu(OAc)(2)-bis(oxazolines) via hydrogen bonding by SBA-15 was applied to asymmetric Henry reaction, and good enantioselectivities were obtained (up to 83% ee) between 2-methoxybenzaldehyde and CH(3)NO(2) in isopropyl alcohol (iPrOH). The catalyst could be reused seven times without any obvious
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