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Safety Information

516325

Sigma-Aldrich

4-Methoxy-2-methylbenzaldehyde

95%

Synonym(s):

2-Methyl-p-anisaldehyde

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About This Item

Linear Formula:
CH3C6H3(OCH3)CHO
CAS Number:
52289-54-0
Molecular Weight:
150.17
MDL number:
MFCD02261771
UNSPSC Code:
12352100
PubChem Substance ID:
24873879
NACRES:
NA.22

Assay

95%

refractive index

n20/D 1.571 (lit.)

bp

262-267 °C (lit.)

density

1.107 g/mL at 25 °C (lit.)

SMILES string

[H]C(=O)c1ccc(OC)cc1C

InChI

1S/C9H10O2/c1-7-5-9(11-2)4-3-8(7)6-10/h3-6H,1-2H3

InChI key

WICYVKGMEJSDAO-UHFFFAOYSA-N

Storage Class Code

12 - Non Combustible Liquids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

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

516325-5G:
516325-BULK:
516325-VAR:

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Certificates of Analysis (COA)

Lot/Batch Number
MKBG0955V
10930DH
07318ME
05928HE
07822KD

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Compounds of potential interest for the chemotherapy of leprosy.
Buu-Hoi NP, et al.
The Journal of Organic Chemistry, 21(4), 415-418 (1956)
Estrogenic Biphenyls. III. 2-Alkyl-4-methoxybiphenyl-4'-carboxylic Acids.
Sato T and Oki M.
Bulletin of the Chemical Society of Japan, 30(8), 859-862 (1957)
Tamer Awad et al.
Journal of chromatographic science, 45(8), 458-465 (2007-11-21)
The methoxy methyl phenylacetones share an isobaric relationship (equivalent mass but different elemental composition) to the controlled precursor substance 3,4-methylenedioxyphenylacetone. The 10 methoxy methyl phenylacetones as well as the methylenedioxyphenylacetones show essentially equivalent mass spectra with major fragment ions at
Jong H Kim et al.
Annals of clinical microbiology and antimicrobials, 10, 23-23 (2011-06-02)
Disruption of cellular antioxidation systems should be an effective method for control of fungal pathogens. Such disruption can be achieved with redox-active compounds. Natural phenolic compounds can serve as potent redox cyclers that inhibit microbial growth through destabilization of cellular

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