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360910

Sigma-Aldrich

Methyl 3-(4-hydroxyphenyl)propionate

97%

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About This Item

Fórmula linear:
HOC6H4CH2CH2CO2CH3
Número CAS:
5597-50-2
Peso molecular:
180.20
Número MDL:
MFCD00071577
Código UNSPSC:
12352100
ID de substância PubChem:
24862009
NACRES:
NA.22

Ensaio

97%

pb

108 °C/11 mmHg (lit.)

pf

39-41 °C (lit.)

cadeia de caracteres SMILES

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

chave InChI

XRAMJHXWXCMGJM-UHFFFAOYSA-N

Descrição geral

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

Aplicação

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

Pictogramas

Exclamation mark
GHS07

Palavra indicadora

Warning

Frases de perigo

H315,H319,H335

Classificações de perigo

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

Órgãos-alvo

Respiratory system

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

235.4 °F - closed cup

Ponto de fulgor (°C)

113 °C - closed cup

Equipamento de proteção individual

dust mask type N95 (US), Eyeshields, Gloves

Certificados de análise (COA)

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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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