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

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
  • C19H26ClN5O2
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  • 3-(4-fluorophenyl)-9-(2-methylpropyl)-9,10-dihydro-4H,8H-chromeno[8,7-e][1,3]oxazin-4-one
  • N-[(2Z)-5-(2-methylpropyl)-1,3,4-thiadiazol-2(3H)-ylidene]-3-phenyl-5,6-dihydro-1,4-oxathiine-2-carboxamide
  • 3-(3,4-dimethoxyphenyl)-9-(2-methoxyethyl)-2-methyl-9,10-dihydrochromeno[8,7-e][1,3]oxazin-4(8H)-one
  • N-[1-(3-methoxypropyl)-4,5-dimethyl-3-(phenylsulfonyl)-1H-pyrrol-2-yl]-3-methylbutanamide
  • 3-(1,3-Benzodioxol-5-yl)-6-(3-bromo-4-fluorophenyl)[1,2,4]triazolo[3,4-b][1,3,4]thiadiazole
  • N-{1-(2-methoxyethyl)-3-[(4-methoxyphenyl)sulfonyl]-4,5-dimethyl-1H-pyrrol-2-yl}butanamide
  • N-(4-fluorophenyl)-3-([1,2,4]triazolo[4,3-a]pyridin-3-yl)propanamide
  • C13H18N4O3S2
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