Skip to Content
Merck
All Photos(1)

Key Documents

View All Documentation

N7000

Sigma-Aldrich

1-Naphthyl phosphate monosodium salt monohydrate

≥98% (titration), powder

Synonym(s):

α-Naphthyl phosphate monosodium salt monohydrate, Sodium 1-naphthyl phosphate monohydrate

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Linear Formula:
C10H7OP(O)(OH)(ONa) · H2O
CAS Number:
81012-89-7
Molecular Weight:
264.15
Beilstein:
1877764
MDL number:
MFCD00150615
UNSPSC Code:
12352202
PubChem Substance ID:
24897801
NACRES:
NA.77

Quality Level

200

Assay

≥98% (titration)

form

powder

color

white to off-white

solubility

H2O: 50 mg/mL

storage temp.

2-8°C

SMILES string

[Na+].[H]O[H].OP([O-])(=O)Oc1cccc2ccccc12

InChI

1S/C10H9O4P.Na.H2O/c11-15(12,13)14-10-7-3-5-8-4-1-2-6-9(8)10;;/h1-7H,(H2,11,12,13);;1H2/q;+1;/p-1

InChI key

NSWUDGODQXQNON-UHFFFAOYSA-M

Looking for similar products? Visit Product Comparison Guide

Application

1-Naphthyl phosphate monosodium salt monohydrate has been used as a non-specific phosphatase inhibitor in the splice correction assay in HeLa pLuc 705 cells.
Preferred substrate for bioanalytical determinations of acid phosphatases, such as prostatic acid phosphatase.

Biochem/physiol Actions

Non-specific phosphatase inhibitor. Inhibits acid, alkaline and protein phosphatases.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

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

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

NickFects, phosphorylated derivatives of transportan 10 for cellular delivery of oligonucleotides
Oskolkov N, et al.
International Journal of Peptide Research and Therapeutics, 17(2), 147-157 (2011)
Koli Taghizadeh et al.
Nature protocols, 3(8), 1287-1298 (2008-08-21)
The analysis of damage products as biomarkers of inflammation has been hampered by a poor understanding of the chemical biology of inflammation, the lack of sensitive analytical methods and a focus on single chemicals as surrogates for inflammation. To overcome
Keren B Turton et al.
PloS one, 10(5), e0127243-e0127243 (2015-05-20)
Signal transducer and activator of transcription 3 (STAT3) is a key mediator of leukocyte differentiation and proliferation. The 3' end of STAT3 transcripts is subject to two alternative splicing events. One results in either full-length STAT3α or in STAT3β, which
Manuela Piazzi et al.
FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 29(4), 1383-1394 (2015-01-01)
The phosphoinositide-dependent signal transduction pathway has been implicated in the control of a variety of biologic processes, such as the regulation of cellular metabolism and homeostasis, cell proliferation and differentiation, and apoptosis. One of the key players in the regulation
Luis Alberto Luévano-Martínez et al.
Biochimica et biophysica acta, 1847(6-7), 587-598 (2015-04-07)
Mitochondria play a key role in adaptation during stressing situations. Cardiolipin, the main anionic phospholipid in mitochondrial membranes, is expected to be a determinant in this adaptive mechanism since it modulates the activity of most membrane proteins. Here, we used
View All Related Papers

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service