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360910

Sigma-Aldrich

Methyl-3-(4-hydroxyphenyl)propionat

97%

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About This Item

Lineare Formel:
HOC6H4CH2CH2CO2CH3
CAS-Nummer:
5597-50-2
Molekulargewicht:
180.20
MDL-Nummer:
MFCD00071577
UNSPSC-Code:
12352100
PubChem Substanz-ID:
24862009
NACRES:
NA.22

Assay

97%

bp

108 °C/11 mmHg (lit.)

mp (Schmelzpunkt)

39-41 °C (lit.)

SMILES String

COC(=O)CCc1ccc(O)cc1

InChI

1S/C10H12O3/c1-13-10(12)7-4-8-2-5-9(11)6-3-8/h2-3,5-6,11H,4,7H2,1H3

InChIKey

XRAMJHXWXCMGJM-UHFFFAOYSA-N

Allgemeine Beschreibung

Methyl 3-(4-hydroxyphenyl)propionate is reported to be responsible for biological nitrification inhibition in sorghum (Sorghum bicolor).

Anwendung

Methyl 3-(4-hydroxyphenyl)propionate may be used in the enzymatic coupling of saccharides to protein.

Piktogramme

Exclamation mark
GHS07

Signalwort

Warning

Gefahreneinstufungen

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

Zielorgane

Respiratory system

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

235.4 °F - closed cup

Flammpunkt (°C)

113 °C - closed cup

Persönliche Schutzausrüstung

dust mask type N95 (US), Eyeshields, Gloves

Analysenzertifikate (COA)

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4-Hydroxy-phenylbrenztraubensäure 98%

Sigma-Aldrich

114286

4-Hydroxy-phenylbrenztraubensäure

N-Allylthioharnstoff 98%

Sigma-Aldrich

108804

N-Allylthioharnstoff

Dicyandiamid 99%

Sigma-Aldrich

D76609

Dicyandiamid

Methyllinoleat ≥98% (GC)

Sigma-Aldrich

L1876

Methyllinoleat

Ruud ter Haar et al.
Carbohydrate research, 346(8), 1005-1012 (2011-04-14)
To enable enzymatic coupling of saccharides to proteins, several di- and trisaccharides were hydroxy-arylated using anhydrous transesterification with methyl 3-(4-hydroxyphenyl)propionate, catalyzed by potassium carbonate. This transesterification resulted in the attachment of up to 3 hydroxy-aryl units per oligosaccharide molecule, with
Hossain A K M Zakir et al.
The New phytologist, 180(2), 442-451 (2008-07-29)
Nitrification results in poor nitrogen (N) recovery and negative environmental impacts in most agricultural systems. Some plant species release secondary metabolites from their roots that inhibit nitrification, a phenomenon known as biological nitrification inhibition (BNI). Here, we attempt to characterize
Andre P Martinez et al.
Biomacromolecules, 18(6), 2000-2011 (2017-05-20)
A series of biodegradable drug delivery polymers with intrinsic multifunctionality have been designed and synthesized utilizing a polyphosphazene macromolecular engineering approach. Novel water-soluble polymers, which contain carboxylic acid and pyrrolidone moieties attached to an inorganic phosphorus-nitrogen backbone, were characterized by
Alexander K Andrianov et al.
Biomacromolecules, 19(8), 3467-3478 (2018-06-29)
Novel oppositely charged polyphosphazene polyelectrolytes containing grafted poly(ethylene glycol) (PEG) chains were synthesized as modular components for the assembly of biodegradable PEGylated protein delivery vehicles. These macromolecular counterparts, which contained either carboxylic acid or tertiary amino groups, were then formulated

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