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218995

N,N-Dimethyl-1-naphthylamine

Name: <I>N</I>,<I>N</I>-Dimethyl-1-naphthylamine
Brand: ALDRICH

99%

Synonym(s):

1-Dimethylaminonaphthalene

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About This Item

Linear Formula:

C₁₀H₇N(CH₃)₂

CAS Number:

86-56-6

Molecular Weight:

171.24

EC Number:

201-682-4

UNSPSC Code:

12171500

PubChem Substance ID:

329752218

Beilstein/REAXYS Number:

1424075

MDL number:

MFCD00003919

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Properties

assay

99%

refractive index

n20/D 1.622 (lit.)

bp

139-140 °C/13 mmHg (lit.)

density

1.042 g/mL at 25 °C (lit.)

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

Description

pictograms

GHS07,GHS09

signalword

Warning

hcodes

H302,H411

pcodes

P264 - P270 - P273 - P301 + P312 - P391 - P501

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Chronic 2

Storage Class

10 - Combustible liquids

wgk

WGK 2

flash_point_f

235.4 °F - closed cup

flash_point_c

113 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

Regulatory Information

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[Sensitivity of methods for determining nitrites].

P A Kal'tianis et al.

Laboratornoe delo, (3)(3), 27-28 (1982-01-01)

Detection of bacterial nitrate reductase activity by the use of a powdered reagent and rapid swab methods as compared to the conventional test.

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

Fluorescence study of domain structure and lipid interaction of human apolipoproteins E3 and E4.

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

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