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Key Documents

793833

Sigma-Aldrich

Methylammonium triiodoplumbate(II) precursor solution

greener alternative

40 wt. % in DMF

Synonyme(s) :

Methanamine, triiodoplumbate(1−), Methylamine triiodoplumbate(1−), Methylammonium triiodoplumbate(1−), Plumbate(1−), triiodo-, hydrogen, compound with methanamine (1:1)

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About This Item

Formule linéaire :
[CH3NH3]+[PbI3]-
Poids moléculaire :
619.98
Code UNSPSC :
12352302

Forme

solution

Caractéristiques du produit alternatif plus écologique

Design for Energy Efficiency
Learn more about the Principles of Green Chemistry.

sustainability

Greener Alternative Product

Concentration

40 wt. % in DMF

Indice de réfraction

n20/D 1.520

Densité

1.368 g/mL at 25 °C

λmax

321 nm

Autre catégorie plus écologique

, Enabling

Application

Methylammonium lead iodide is a well studied precursor for the deposition of perovskite active layers for advanced photovoltaics

Pictogrammes

Health hazardExclamation markEnvironment
GHS08,GHS07,GHS09

Mention d'avertissement

Danger

Classification des risques

Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Irrit. 2 - Repr. 1A - STOT RE 2

Code de la classe de stockage

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

141.0 °F

Point d'éclair (°C)

60.56 °C

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Certificats d'analyse (COA)

Lot/Batch Number
MKCJ2578
MKBS6438V

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Retrouvez la documentation relative aux produits que vous avez récemment achetés dans la Bibliothèque de documents.

Consulter la Bibliothèque de documents

Nam Joong Jeon et al.
Journal of the American Chemical Society, 135(51), 19087-19090 (2013-12-10)
A set of three N,N-di-p-methoxyphenylamine-substituted pyrene derivatives have successfully been synthesized and characterized by (1)H/(13)C NMR spectroscopy, mass spectrometry, and elemental analysis. The optical and electronic structures of the pyrene derivatives were adjusted by controlling the ratio of N,N-di-p-methoxyphenylamine to

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