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360910

Methyl 3-(4-hydroxyphenyl)propionate

Name: Methyl 3-(4-hydroxyphenyl)propionate
Brand: ALDRICH

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About This Item

Linear Formula:

HOC₆H₄CH₂CH₂CO₂CH₃

CAS Number:

5597-50-2

Molecular Weight:

180.20

NACRES:

NA.22

PubChem Substance ID:

24862009

UNSPSC Code:

12352100

MDL number:

MFCD00071577

Assay:

97%

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Properties

Quality Level

200

assay

97%

bp

108 °C/11 mmHg (lit.)

mp

39-41 °C (lit.)

functional group

ester

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

InChI key

XRAMJHXWXCMGJM-UHFFFAOYSA-N

Description

General description

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

Application

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

pictograms

GHS07

signalword

Warning

hcodes

H315,H319,H335

pcodes

P261 - P264 - P271 - P280 - P302 + P352 - P305 + P351 + P338

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

235.4 °F - closed cup

flash_point_c

113 °C - closed cup

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Detection, isolation and characterization of a root-exuded compound, methyl 3-(4-hydroxyphenyl) propionate, responsible for biological nitrification inhibition by sorghum (Sorghum bicolor).

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

Proof of principle for the synthesis of hydroxy-aryl esters of glycosidic polyols and non-reducing oligosaccharides with subsequent enzymatic coupling to a tyrosine-containing tripeptide.

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

Biodegradable "Smart" Polyphosphazenes with Intrinsic Multifunctionality as Intracellular Protein Delivery Vehicles.

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

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Global Trade Item Number

SKU	GTIN
360910-5G	04061831810677