D21200

1,5-Diaminonaphthalene

Name: 1,5-Diaminonaphthalene
Brand: ALDRICH

97%

Synonym(s):

1,5-DAN, 1,5-Naphthalenediamine, NSC 401110

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All Photos(3)

About This Item

Linear Formula:

C₁₀H₆(NH₂)₂

CAS Number:

2243-62-1

Molecular Weight:

158.20

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

24893631

EC Number:

218-817-8

Beilstein/REAXYS Number:

907947

MDL number:

MFCD00004029

Product Name

1,5-Diaminonaphthalene, 97%

InChI

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

InChI key

KQSABULTKYLFEV-UHFFFAOYSA-N

SMILES string

Nc1cccc2c(N)cccc12

assay

97%

form

powder

mp

185-187 °C (lit.)

fluorescence

λ_ex 330 nm (H2O:MeOH (1:4))

Quality Level

100

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Related Categories

Organic Building Blocks

pictograms

GHS08,GHS07,GHS09

signalword

Warning

hcodes

H302,H317,H351,H410

pcodes

P202 - P273 - P280 - P301 + P312 - P302 + P352 - P308 + P313

Hazard Classifications

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

Storage Class

11 - Combustible Solids

wgk

WGK 2

flash_point_f

438.8 °F - DIN 51758

flash_point_c

226 °C - DIN 51758

ppe

dust mask type N95 (US), Eyeshields, Gloves

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MALDI-ISD Mass Spectrometry Analysis of Hemoglobin Variants: a Top-Down Approach to the Characterization of Hemoglobinopathies.

Roger Théberge et al.

Journal of the American Society for Mass Spectrometry, 26(8), 1299-1310 (2015-05-24)

Hemoglobinopathies are the most common inherited disorders in humans and are thus the target of screening programs worldwide. Over the past decade, mass spectrometry (MS) has gained a more important role as a clinical means to diagnose variants, and a

1,5-Naphthalenediamine.

IARC monographs on the evaluation of the carcinogenic risk of chemicals to humans, 27, 127-132 (1982-04-01)

Performance of Fe-N/C Oxygen Reduction Electrocatalysts toward NO2-, NO, and NH2OH Electroreduction: From Fundamental Insights into the Active Center to a New Method for Environmental Nitrite Destruction.

Daniel Malko et al.

Journal of the American Chemical Society, 138(49), 16056-16068 (2016-12-15)

Although major progress has recently been achieved through ex situ methods, there is still a lack of understanding of the behavior of the active center in non-precious metal Fe-N/C catalysts under operating conditions. Utilizing nitrite, nitric oxide, and hydroxylamine as

Antifungal Activity of an Original Amino-Isocyanonaphthalene (ICAN) Compound Family: Promising Broad Spectrum Antifungals.

Miklós Nagy et al.

Molecules (Basel, Switzerland), 25(4) (2020-02-23)

: Multiple drug resistant fungi pose a serious threat to human health, therefore the development of completely new antimycotics is of paramount importance. The in vitro antifungal activity of the original, 1-amino-5-isocyanonaphthalenes (ICANs) was evaluated against reference strains of clinically

Amorphous Porous Organic Polymers Based on Schiff-Base Chemistry for Highly Efficient Iodine Capture.

Zongxia Guo et al.

Chemistry, an Asian journal (2018-06-07)

Porous organic polymers (POPs) have been considered as prominent adsorbents for volatile iodine. So far, both crystalline and amorphous POPs have accomplished excellent iodine capture capability. Considering the difficulty and challenges in preparing perfect crystalline POPs, more explorations into developing

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