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104043

Sigma-Aldrich

N-Phenyl-1-naphthylamine

reagent grade, 98%

Sinonimo/i:

1-(N-phenylamino)naphthalene, N-(1-Naphthyl)aniline, NPN

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About This Item

Formula condensata:
C10H7NHC6H5
Numero CAS:
90-30-2
Peso molecolare:
219.28
Beilstein:
2211174
Numero CE:
201-983-0
Numero MDL:
MFCD00003878
Codice UNSPSC:
12352100
ID PubChem:
57646802
NACRES:
NA.22

Grado

reagent grade

Livello qualitativo

100

Saggio

98%

Forma fisica

solid

P. eboll.

226 °C/15 mmHg (lit.)

Punto di fusione

60-62 °C (lit.)

λmax

252 nm

Stringa SMILE

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
XQVWYOYUZDUNRW-UHFFFAOYSA-N

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Applicazioni

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 .

Azioni biochim/fisiol

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

Avvertenze

Warning

Indicazioni di pericolo

H302,H317,H373,H410

Classi di pericolo

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

Organi bersaglio

Blood

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 2

Dispositivi di protezione individuale

dust mask type N95 (US), Eyeshields, Gloves

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Certificati d'analisi (COA)

Lot/Batch Number
MKCQ9154
MKCQ0246
MKCM7486
MKCL9782
MKCJ1873

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Sigma-Aldrich

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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.
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The Journal of Organic Chemistry, 46(1), 219-220 (1981)
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