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Merck
CN

D4011

N,N-Dimethyl-1-naphthylamine

≥98.0% purity (GC), liquid

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
NACRES:
NA.47
PubChem Substance ID:
24893807
UNSPSC Code:
12171500
EC Number:
201-682-4
MDL number:
MFCD00003919
Beilstein/REAXYS Number:
1424075

Key Documents

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Product Name

N,N-Dimethyl-1-naphthylamine, ≥98.0% (GC)

InChI key

AJUXDFHPVZQOGF-UHFFFAOYSA-N

InChI

1S/C12H13N/c1-13(2)12-9-5-7-10-6-3-4-8-11(10)12/h3-9H,1-2H3

SMILES string

CN(C)c1cccc2ccccc12

assay

≥98.0% (GC)

form

liquid

technique(s)

titration: suitable

color

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.)

application(s)

diagnostic assay manufacturing
hematology
histology

storage temp.

room temp

Quality Level

200

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Application

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.

Biochem/physiol Actions

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.

General description

N,N-Dimethyl-1-naphthylamine is an aromatic amine and a dye.

pictograms

Exclamation markEnvironment
GHS07,GHS09

signalword

Warning

hcodes

H302,H411

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

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Certificates of Analysis (COA)

Lot/Batch Number
STBH3022
STBH1421
STBD7716V
STBB8424V
1428809

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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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