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Key Documents

N2752

Sigma-Aldrich

4-Nitrophenyl palmitate

lipase substrate, chromogenic, ≥98% (TLC), powder

Synonyme(s) :

p-Nitrophenyl palmitate, Hexadecanoic acid 4-nitrophenyl ester

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About This Item

Formule empirique (notation de Hill):
C22H35NO4
Numéro CAS:
Poids moléculaire :
377.52
Numéro Beilstein :
1891754
Numéro CE :
Numéro MDL:
Code UNSPSC :
12352204
ID de substance PubChem :
Nomenclature NACRES :
NA.83

product name

4-Nitrophenyl palmitate, lipase substrate

Niveau de qualité

Pureté

≥98% (TLC)

Forme

powder

Solubilité

chloroform: 100 mg/mL, clear, colorless to faintly yellow

Température de stockage

−20°C

Chaîne SMILES 

CCCCCCCCCCCCCCCC(=O)Oc1ccc(cc1)[N+]([O-])=O

InChI

1S/C22H35NO4/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-22(24)27-21-18-16-20(17-19-21)23(25)26/h16-19H,2-15H2,1H3

Clé InChI

LVZSQWIWCANHPF-UHFFFAOYSA-N

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Description générale

4-Nitrophenyl palmitate is a substrate for lipase enzyme activity. Lipase hydrolyzes 4-nitrophenyl palmitate and yields the yellow colored product 4-nitrophenol, which is measurable spectrophotometrically at 410 nm. This method is advantageous due to its short reaction time and facile spectrophotometric analyses. The cell-bound lipase has preference for 4-nitrophenyl palmitate as substrate than the extracellular lipase.

Application

4-nitrophenyl palmitate has been used as a substrate for lipase enzyme activity.

Pictogrammes

Exclamation mark

Mention d'avertissement

Warning

Mentions de danger

Conseils de prudence

Classification des risques

Skin Sens. 1

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

dust mask type N95 (US), Eyeshields, Faceshields, Gloves


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Consulter la Bibliothèque de documents

M M Maia et al.
Bioresource technology, 76(1), 23-27 (2001-04-24)
Lipase (Glycerol ester hydrolase EC 3.1.1.3.) from a Brazilian strain of Fusarium solani FSI has been investigated. The effect of different carbon sources and trace elements added to basal medium was observed with the aim of improving enzyme production. Lipase
Shamoon Asmat et al.
Materials science & engineering. C, Materials for biological applications, 99, 25-36 (2019-03-21)
Herein, as a promising support, a magnetic enzyme nanoformulation have been designed and fabricated by a poly-o-toluidine modification approach. Owing to the magnetic nature and the existence of amine functionalized groups, the as-synthesised poly(o-toluidine) functionalized magnetic nanocomposite (Fe3O4@POT) was employed
Seon-Woo Lee et al.
Applied microbiology and biotechnology, 65(6), 720-726 (2004-09-15)
The construction and screening of metagenomic libraries constitute a valuable resource for obtaining novel biocatalysts. In this work, we present the construction of a metagenomic library in Escherichia coli using fosmid and microbial DNA directly isolated from forest topsoil and
Lipase and biosurfactant from Ochrobactrum intermedium strain MZV101 isolated by washing powder for detergent application
Zarinviarsagh M, et al.
Lipids in Health and Disease, 16(1), 177-177 (2017)
Kai Yuan et al.
Journal of industrial microbiology & biotechnology, 46(8), 1091-1101 (2019-06-21)
Metabolic fluxes during lipase production by Bacillus subtilis CICC 20034 in synthetic medium were studied using metabolic flux analysis (MFA). The MFA showed that lipase production was dependent on, and coupled to the tributyrin uptake rate, formation of biomass, lactate

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