lead selenide

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Names

[ CAS No. ]:
12069-00-0

[ Name ]:
lead selenide

[Synonym ]:
MFCD00016273
EINECS 235-109-4

Chemical & Physical Properties

[ Density]:
8.1 g/cm3

[ Melting Point ]:
1065ºC

[ Molecular Formula ]:
HPbSe

[ Molecular Weight ]:
287.16800

[ Exact Mass ]:
288.90100

MSDS

Click to get detail MSDS

Safety Information

[ Symbol ]:

GHS06, GHS08, GHS09

[ Signal Word ]:
Danger

[ Hazard Statements ]:
H301 + H331-H302 + H332-H360Df-H373-H410

[ Precautionary Statements ]:
Missing Phrase - N15.00950417-P201-P260-P280-P304 + P340 + P312-P308 + P313

[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves

[ Hazard Codes ]:
Xn

[ Risk Phrases ]:
20/22-33

[ Safety Phrases ]:
22-26-28-36/37/39-45

[ RIDADR ]:
UN 3288

[ Packaging Group ]:
II

[ Hazard Class ]:
6.1(a)

Articles

Optical fiber amplifiers based on PbS/CdS QDs modified by polymers.

Opt. Express 21(7) , 8214-9, (2013)

Optical fiber amplifiers based on PbS/CdS semiconductor quantum dots (QDs) modified by an amphiphilic polymer were demonstrated. Well-defined QDs and an amphiphilic copolymer were first prepared and t...

Triplet exciton dissociation in singlet exciton fission photovoltaics.

Adv. Mater. 24(46) , 6169-74, (2012)

Triplet exciton dissociation in singlet exciton fission devices with three classes of acceptors are characterized: fullerenes, perylene diimides, and PbS and PbSe colloidal nanocrystals. Using photocu...

Infrared colloidal lead chalcogenide nanocrystals: synthesis, properties, and photovoltaic applications.

Nanoscale 4(7) , 2187-201, (2012)

Simple solution phase, catalyst-free synthetic approaches that offer monodispersed, well passivated, and non-aggregated colloidal semiconductor nanocrystals have presented many research opportunities ...


More Articles

Related Compounds

  • Lead selenide
  • lead selenide,99.9
  • lead selenide telluride
  • lead(ii) tartrate
  • lead benzoate
  • lead germanate
  • (2S,4R)-4-hydroxy-1-[(2S)-2-[[2-[2-(2-hydroxyethoxy)ethoxy]acetyl]amino]-3,3-dimethyl-butanoyl]-N-[[4-(4-methylthiazol-5-yl)phenyl]methyl]pyrrolidine-2-carboxamide
  • (E)-4-[2-[2-[2-[2-[2-[2-(2,6-dioxo-3-piperidyl)-1,3-dioxo-isoindolin-4-yl]oxyethoxy]ethoxy]ethoxy]ethoxy]ethoxy]but-2-enoic acid
  • 7-[2-[2-[2-[2-[2-(2,6-Dioxo-3-piperidyl)-1,3-dioxo-isoindolin-4-yl]oxyethoxy]ethoxy]ethoxy]ethoxy]heptanoic acid
  • (2S,4R)-1-[(2S)-2-[[2-(4-chlorobutoxy)acetyl]amino]-3,3-dimethyl-butanoyl]-4-hydroxy-N-[[4-(4-methylthiazol-5-yl)phenyl]methyl]pyrrolidine-2-carboxamide
  • (2S,4R)-1-[(2S)-2-(4-bromobutanoylamino)-3,3-dimethyl-butanoyl]-4-hydroxy-N-[[4-(4-methylthiazol-5-yl)phenyl]methyl]pyrrolidine-2-carboxamide
  • 4-[2-[3-[3-(3-Benzyloxypropoxy)propoxy]propoxy]ethylamino]-2-(2,6-dioxo-3-piperidyl)isoindoline-1,3-dione
  • N-[2-(2,6-dioxo-3-piperidyl)-1,3-dioxo-isoindolin-4-yl]-6-[2-(2-oct-7-ynoxyethoxy)ethoxy]hexanamide
  • 4-[2-[2-[2-[2-(2-Benzyloxyethoxy)ethoxy]ethoxy]ethoxy]ethoxy]-2-(2,6-dioxo-3-piperidyl)isoindoline-1,3-dione
  • (2S,4R)-1-[(2S)-3,3-dimethyl-2-(4-piperazin-1-ylbutanoylamino)butanoyl]-4-hydroxy-N-[[4-(4-methylthiazol-5-yl)phenyl]methyl]pyrrolidine-2-carboxamide
  • tert-butyl N-[3-(4-azidobutoxy)propyl]-N-[3-[[2-(2,6-dioxo-3-piperidyl)-1-oxo-isoindolin-4-yl]amino]-3-oxo-propyl]carbamate
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