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793833

Methylammonium triiodoplumbate(II) precursor solution

greener alternative

40 wt. % in DMF

Synonym(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

Linear Formula:
[CH3NH3]+[PbI3]-
Molecular Weight:
619.98
UNSPSC Code:
12352302
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solution

greener alternative product characteristics

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concentration

40 wt. % in DMF

refractive index

n20/D 1.520

density

1.368 g/mL at 25 °C

λmax

321 nm

greener alternative category

, Enabling

Application

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

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Danger

Hazard Classifications

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

Storage Class

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

wgk

WGK 3

flash_point_f

141.0 °F

flash_point_c

60.56 °C

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

Class I Designated Chemical Substances

prtr

Group 4: Flammable liquids + Type 2 petroleums + Hazardous rank III + Water insoluble liquid

fsl

Substances Subject to be Indicated Names

ishl_indicated

Substances Subject to be Notified Names

ishl_notified

793833-5ML:4548173914282 + 793833-VAR: + 793833-BULK:

jan

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Certificates of Analysis (COA)

Lot/Batch Number
MKCJ2578
MKBS6438V

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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