추천 제품
제품명
N,N-Dimethyl-1-naphthylamine, ≥98.0% (GC)
Quality Level
분석
≥98.0% (GC)
양식
liquid
기술
titration: suitable
색상
faint yellow to dark yellow
refractive index
n20/D 1.622 (lit.)
bp
139-140 °C/13 mmHg (lit.)
density
1.042 g/mL at 25 °C (lit.)
응용 분야
diagnostic assay manufacturing
hematology
histology
저장 온도
room temp
SMILES string
CN(C)c1cccc2ccccc12
InChI
1S/C12H13N/c1-13(2)12-9-5-7-10-6-3-4-8-11(10)12/h3-9H,1-2H3
InChI key
AJUXDFHPVZQOGF-UHFFFAOYSA-N
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일반 설명
N,N-Dimethyl-1-naphthylamine is an aromatic amine and a dye.
애플리케이션
N,N-Dimethyl-1-naphthylamine (1-Dimethylaminonaphthalene) is used to study nitrate reduction by organisms. Reduction of nitrate results in the formation of nitrite, which reacts with sulfanilic acid and 1-dimethylaminonaphthalene to form a red diazo dye.
생화학적/생리학적 작용
N,N-Dimethyl-1-naphthylamine (1-Dimethylaminonaphthalene) is used to study nitrate reduction by organisms. Reduction of nitrate results in the formation of nitrite, which reacts with sulfanilic acid and 1-dimethylaminonaphthalene to form a red diazo dye.
신호어
Warning
유해 및 위험 성명서
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Chronic 2
Storage Class Code
10 - Combustible liquids
WGK
WGK 2
Flash Point (°F)
235.4 °F - closed cup
Flash Point (°C)
113 °C - closed cup
개인 보호 장비
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
이미 열람한 고객
Washington JA
Laboratory Procedures in Clinical Microbiology (2012)
[Sensitivity of methods for determining nitrites].
P A Kal'tianis et al.
Laboratornoe delo, (3)(3), 27-28 (1982-01-01)
L Ingham et al.
Zentralblatt fur Bakteriologie : international journal of medical microbiology, 279(2), 225-230 (1993-06-01)
A rapid swab method using either a dry or moist swab soaked with potassium nitrate/benzalkonium chloride solution, and a method employing a single powdered reagent were assessed as possible alternatives to the conventional test for the detection of bacterial nitrate
Chiharu Mizuguchi et al.
Biochimica et biophysica acta, 1841(12), 1716-1724 (2014-10-05)
Human apolipoprotein E (apoE) isoforms exhibit different conformational stabilities and lipid-binding properties that give rise to altered cholesterol metabolism among the isoforms. Using Trp-substituted mutations and site- directed fluorescence labeling, we made a comprehensive comparison of the conformational organization of
Jonas Camillus Jeppesen et al.
Langmuir : the ACS journal of surfaces and colloids, 31(46), 12699-12707 (2015-10-27)
Gel domains in lipid bilayers are structurally more complex than fluid domains. Growth dynamics can lead to noncircular domains with a heterogeneous orientational texture. Most model membrane studies involving gel domain morphology and lateral organization assume the domains to be
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