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Merck
모든 사진(2)

주요 문서

104043

Sigma-Aldrich

N-Phenyl-1-naphthylamine

reagent grade, 98%

동의어(들):

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

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500 G
₩156,513

₩156,513


출고 가능일2025년 4월 10일세부사항


벌크 견적 요청

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500 G
₩156,513

About This Item

Linear Formula:
C10H7NHC6H5
CAS Number:
Molecular Weight:
219.28
Beilstein:
2211174
EC Number:
MDL number:
UNSPSC 코드:
12352100
PubChem Substance ID:
NACRES:
NA.22

₩156,513


출고 가능일2025년 4월 10일세부사항


벌크 견적 요청

Grade

reagent grade

Quality Level

분석

98%

양식

solid

bp

226 °C/15 mmHg (lit.)

mp

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

InChI key

XQVWYOYUZDUNRW-UHFFFAOYSA-N

유사한 제품을 찾으십니까? 방문 제품 비교 안내

애플리케이션

N-Phenyl-1-naphthylamine can be used as fluorescent probe for the determination of critical micelle concentration of surfactants[1]. N-Phenyl-1-naphthylamine was used in a method for determination of the concentration of organolithium and organomagnesium reagents[2]. N-Phenyl-1-naphthylamine was used as hydrophobic probe to study the phase transitions of membrane lipids in whole cells [3].

생화학적/생리학적 작용

N-Phenyl-1-naphthylamine turns fluorescent after binding to hydrophobic regions of cell membranes[4].

픽토그램

Health hazardExclamation markEnvironment

신호어

Warning

유해 및 위험 성명서

Hazard Classifications

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

표적 기관

Blood

Storage Class Code

11 - Combustible Solids

WGK

WGK 2

개인 보호 장비

dust mask type N95 (US), Eyeshields, Gloves


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R N Reusch et al.
Proceedings of the National Academy of Sciences of the United States of America, 85(12), 4176-4180 (1988-06-01)
A poly-beta-hydroxybutyrate complex extracted from the plasma membranes of genetically competent Escherichia coli contained polyhydroxybutyrate:polyphosphate:calcium in molar ratios approximating 1:1:0.5. The chain length of the polyhydroxybutyrate was estimated as 120-200 subunits, and that of the polyphosphate was estimated as 130-170
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

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