Skip to Content
Merck
All Photos(2)

Documents

D21405

Sigma-Aldrich

1,8-Diaminonaphthalene

99%

Synonym(s):

1,8-Naphthalenediamine

Sign Into View Organizational & Contract Pricing
All Photos(2)

About This Item

Linear Formula:
C10H6(NH2)2
CAS Number:
479-27-6
Molecular Weight:
158.20
Beilstein:
742841
EC Number:
207-529-8
MDL number:
MFCD00004033
UNSPSC Code:
12352100
PubChem Substance ID:
24893638
NACRES:
NA.22

Quality Level

200

Assay

99%

form

crystals

bp

205 °C/12 mmHg (lit.)

mp

60-65 °C (lit.)

SMILES string

Nc1cccc2cccc(N)c12

InChI

1S/C10H10N2/c11-8-5-1-3-7-4-2-6-9(12)10(7)8/h1-6H,11-12H2

InChI key

YFOOEYJGMMJJLS-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Signal Word

Warning

Hazard Statements

H302,H317,H351,H410

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Carc. 2 - Skin Sens. 1

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

>392.0 °F - closed cup

Flash Point(C)

> 200 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Customers Also Viewed

Slide 1 of 3

1 of 3

8-AMINO-1-NAPHTHOL AldrichCPR

T285277

8-AMINO-1-NAPHTHOL

1,5-Diaminonaphthalene matrix substance for MALDI-MS, ≥99.0% (HPLC)

Supelco

56451

1,5-Diaminonaphthalene

1,8-DICHLORONAPHTHALENE AldrichCPR

T283169

1,8-DICHLORONAPHTHALENE

Guanzhao Wu et al.
Research (Washington, D.C.), 2019, 6717104-6717104 (2019-09-25)
3D chirality of sandwich type of organic molecules has been discovered. The key element of this chirality is characterized by three layers of structures that are arranged nearly in parallel fashion with one on top and one down from the
Kai Schickedanz et al.
Chemical communications (Cambridge, England), 51(87), 15808-15810 (2015-09-15)
The high-yield synthesis of a boron-doped [4]helicene was achieved through a Ni-mediated Yamamoto C-C-coupling reaction; the moderate distortion of the molecular scaffold confers excellent solubility to the air- and water-stable green luminophore.
Roman Papoušek et al.
Journal of separation science, 42(8), 1629-1633 (2019-02-15)
Masking derivatization was introduced for the determination of residual solvents in samples containing a volatile reactive matrix component(s). Isobutylboronic acid, used in the last step of Bortezomib synthesis, represents a compound passing to the gas phase and deteriorating a chromatographic
Liliana Martínez-Ávila et al.
Environmental pollution (Barking, Essex : 1987), 271, 116358-116358 (2021-01-02)
Polyaromatic phenanthrene (Phe) and benzo[a]pyrene (BaP) are highly toxic, mutagenic, and carcinogenic contaminants widely dispersed in nature, including saline environments. Polyextremotolerant Rhodotorula mucilaginosa EXF-1630, isolated from Arctic sea ice, was grown on a huge concentration range -10 to 500 ppm- of
Mohan N Patel et al.
Bioorganic & medicinal chemistry, 17(15), 5648-5655 (2009-07-08)
Here in we tried to increase an antibacterial activity of ciprofloxacin drug due to formation of mixed-ligand complexes. Synthesized compounds were found to be more potent compare to drugs, ligands and metal salt against selective gram((+ve)) and gram((-ve)) organisms. Interaction

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service