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104043

Sigma-Aldrich

N-Phenyl-1-naphthylamin

reagent grade, 98%

Synonym(e):

1-(N-Phenylamino)-naphthalin, N-(1-Naphthyl)-anilin, NPN

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About This Item

Lineare Formel:
C10H7NHC6H5
CAS-Nummer:
90-30-2
Molekulargewicht:
219.28
Beilstein:
2211174
EG-Nummer:
201-983-0
MDL-Nummer:
MFCD00003878
UNSPSC-Code:
12352100
PubChem Substanz-ID:
57646802
NACRES:
NA.22

Qualität

reagent grade

Qualitätsniveau

100

Assay

98%

Form

solid

bp

226 °C/15 mmHg (lit.)

mp (Schmelzpunkt)

60-62 °C (lit.)

λmax

252 nm

SMILES String

N(c1ccccc1)c2cccc3ccccc23

InChI

1S/C16H13N/c1-2-9-14(10-3-1)17-16-12-6-8-13-7-4-5-11-15(13)16/h1-12,17H

InChIKey

XQVWYOYUZDUNRW-UHFFFAOYSA-N

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Anwendung

N-Phenyl-1-naphthylamine can be used as fluorescent probe for the determination of critical micelle concentration of surfactants. N-Phenyl-1-naphthylamine was used in a method for determination of the concentration of organolithium and organomagnesium reagents. N-Phenyl-1-naphthylamine was used as hydrophobic probe to study the phase transitions of membrane lipids in whole cells .

Biochem./physiol. Wirkung

N-Phenyl-1-naphthylamine turns fluorescent after binding to hydrophobic regions of cell membranes.

Signalwort

Warning

Gefahreneinstufungen

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Skin Sens. 1B - STOT RE 2

Zielorgane

Blood

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 2

Persönliche Schutzausrüstung

dust mask type N95 (US), Eyeshields, Gloves

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Analysenzertifikate (COA)

Lot/Batch Number
MKCQ9154
MKCQ0246
MKCM7486
MKCL9782
MKCJ1873

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1-Naphthylamin 97%

Sigma-Aldrich

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Gewirkte Schwingdrossel L × I.D. 20 m × 0.25 mm, volume 1.0 mL

57410-U

Gewirkte Schwingdrossel

o-Nitrophenyl-β-D-galactopyranosid A β-galactosidase substrate for colorimetric and EIA applications; counterpart of widely used pNPP/alkaline phosphatase substrate.

Sigma-Aldrich

48712-M

o-Nitrophenyl-β-D-galactopyranosid

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International journal of molecular sciences, 19(2) (2018-02-01)
Glucose oxidase (GOD, EC.1.1.3.4) specifically catalyzes the reaction of β-d-glucose to gluconic acid and hydrogen peroxide in the presence of oxygen, which has become widely used in the food industry, gluconic acid production and the feed industry. However, the poor
G M Halliday et al.
Journal of immunological methods, 28(3-4), 381-390 (1979-01-01)
N-phenyl-1-naphthylamine (NPN) becomes fluorescent after binding to hydrophobic regions of cell membranes. Rat and mouse lymphoid cell suspensions stained with NPN showed changes in fluorescence emission 30 min after stimulation with mitogen or antigen, detected by microfluorimetry. Incubation of NPN-labelled
Determination of the critical micelle concentration of surfactants using the fluorescent probe N-phenyl-1-naphthylamine.
Bergbreiter DE and Pendergrass E.
The Journal of Organic Chemistry, 46(1), 219-220 (1981)
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PLoS pathogens, 14(6), e1007084-e1007084 (2018-06-22)
With the antibiotic development pipeline running dry, many fear that we might soon run out of treatment options. High-density infections are particularly difficult to treat due to their adaptive multidrug-resistance and currently there are no therapies that adequately address this
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The Journal of antimicrobial chemotherapy, 64(6), 1203-1211 (2009-10-29)
The emergence of antibiotic resistance has seriously diminished antibiotic efficacy and an increasing number of infections are becoming difficult to treat. One approach to the restoration of antibiotic activity is to administer them in conjunction with non-antibiotic compounds that depress
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