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D4011

N,N-Dimethyl-1-naphthylamine

≥98.0% purity (GC), liquid

Synonym(s):

1-Dimethylaminonaphthalene

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D4011-10ML

$88.40

D4011-25ML

$147.00

D4011-100ML

$525.00

D4011-500ML

$900.00

$88.40


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About This Item

Linear Formula:
C10H7N(CH3)2
CAS Number:
Molecular Weight:
171.24
Beilstein/REAXYS Number:
1424075
EC Number:
MDL number:
UNSPSC Code:
12171500
PubChem Substance ID:
NACRES:
NA.47

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Product Name

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

Quality Level

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

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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1 of 4

This Item
D172405235601D4139
technique(s)

titration: suitable

technique(s)

-

technique(s)

-

technique(s)

titration: suitable

color

faint yellow to dark yellow

color

-

color

-

color

white to light pink, and tan

form

liquid

form

powder or chunks

form

powder

form

powder

application(s)

diagnostic assay manufacturing
hematology
histology

application(s)

diagnostic assay manufacturing
hematology
histology

application(s)

diagnostic assay manufacturing
hematology
histology

application(s)

diagnostic assay manufacturing
hematology
histology

storage temp.

room temp

storage temp.

room temp

storage temp.

room temp

storage temp.

room temp

Quality Level

200

Quality Level

100

Quality Level

100

Quality Level

200

General description

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

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.[1]

pictograms

Exclamation markEnvironment

signalword

Warning

hcodes

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Chronic 2

Storage Class

10 - Combustible liquids

wgk_germany

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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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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