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296880

4-Methoxymandelic acid

98%

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About This Item

Linear Formula:
CH3OC6H4CH(OH)CO2H
CAS Number:
10502-44-0
Molecular Weight:
182.17
NACRES:
NA.22
PubChem Substance ID:
24857884
UNSPSC Code:
12352100
EC Number:
234-031-8
MDL number:
MFCD00004233
Assay:
98%
Form:
solid
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assay

98%

form

solid

mp

108-111 °C (lit.)

SMILES string

COc1ccc(cc1)C(O)C(O)=O

InChI

1S/C9H10O4/c1-13-7-4-2-6(3-5-7)8(10)9(11)12/h2-5,8,10H,1H3,(H,11,12)

InChI key

ITECRQOOEQWFPE-UHFFFAOYSA-N

General description

Chiral separation of the enantiomers of 4-methoxymandelic acid has been reported by a new liquid chromatographic method. The mechanism of veratryl alcohol-mediated oxidation of 4-methoxymandelic acid by lignin peroxidase has been studied by kinetic methods.

Storage Class

13 - Non Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
STBH7229
STBB3035V
STBB3035
S15015
05809KH

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Jie Zhou et al.
Journal of Zhejiang University. Science. B, 14(7), 615-620 (2013-07-05)
A new liquid chromatographic method has been developed for the chiral separation of the enantiomers of mandelic acid and their derivatives 2-chloromandelic acid, 4-hydroxymandelic acid, 4-methoxymandelic acid, and 3,4,5-trismethoxymandelic acid. The enantiomers were separated by a CHIRALPAK(®) IC (250 mm×4.6
Radical cation cofactors in lignin peroxidase catalysis.
P J Harvey et al.
Biochemical Society transactions, 23(2), 262-267 (1995-05-01)
P J Teunissen et al.
FEBS letters, 439(3), 219-223 (1998-12-09)
Poly R478, 4-methoxymandelic acid and oxalic acid were oxidized by lignin peroxidase (LiP) in the presence of the fungal metabolite 2-chloro-1,4-dimethoxybenzene (2Cl-14DMB), whereas no oxidation occurred in the absence of 2Cl-14DMB. These substrates clearly inhibited the consumption of 2Cl-14DMB and
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Global Trade Item Number

SKUGTIN
296880-5G04061831810431