antimony(iii) iodide

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Names

[ CAS No. ]:
7790-44-5

[ Name ]:
antimony(iii) iodide

[Synonym ]:
EINECS 232-205-8
MFCD00016322

Chemical & Physical Properties

[ Density]:
4.92 g/mL at 25ºC(lit.)

[ Boiling Point ]:
401ºC(lit.)

[ Melting Point ]:
170ºC(lit.)

[ Molecular Formula ]:
I3Sb

[ Molecular Weight ]:
502.47300

[ Flash Point ]:
420ºC

[ Exact Mass ]:
501.61700

[ LogP ]:
2.65710

MSDS

Click to get detail MSDS

Safety Information

[ Symbol ]:

GHS07, GHS09

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H302 + H332-H317-H411

[ Precautionary Statements ]:
P261-P280-P301 + P312 + P330

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

[ Hazard Codes ]:
Xn,N

[ Risk Phrases ]:
R20/22

[ Safety Phrases ]:
S61

[ RIDADR ]:
UN 3260 8/PG 2

[ WGK Germany ]:
2

[ Packaging Group ]:
II

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

  • Antimony
  • Antimony trichloride
  • Antimonous hydride
  • molecular iodine
  • ethyldiiodostibine
  • 1,2-diiodotetrafluorobenzene
  • tri-(2-thienyl)-stibine
  • Antimony tribromide
  • perfluoropropyl iodide
  • Bis(heptafluor-n-propyl)-jodphosphan

DownStream

  • Antimony
  • Potassium iodide
  • molecular iodine
  • Phosphorus trichloride
  • Iodine monobromide
  • Antimony tribromide
  • Iodotrifluoromethane
  • tris(trifluoromethyl)stibane
  • Bis(trifluormethyl)-jodstiban

Articles

New antimony(III) halide complexes with dithiocarbamate ligands derived from thiuram degradation: The effect of the molecule's close contacts on in vitro cytotoxic activity.

Mater. Sci. Eng. C. Mater. Biol. Appl. 58 , 396-408, (2015)

Antimony(III) halide complexes of the formulae {[SbBr(Me2DTC)2]n} (1), {[SbI(Me2DTC)2]n} (2) and {[(Me2DTC)2Sb(μ2-I)Sb(Me2DTC)2](+).I3(-)} (3) (Me2DTC = dimethyldithiocarbomate) were synthesized from ...


More Articles

Related Compounds

  • antimony(III)trichloride(TpClBHH)
  • antimony(iii) acetate
  • antimony(III)Br3(TpClBHH)
  • antimony(iii) methoxide
  • Antimony (III) telluride
  • antimony (III) tris(O,O-di-i-butyl phosphorodithioate)
  • (1-(6-(1H-pyrazol-1-yl)pyrimidin-4-yl)azetidin-3-yl)(4-(pyrimidin-2-yl)piperazin-1-yl)methanone
  • 1-(6-(1H-pyrazol-1-yl)pyrimidin-4-yl)-N-(5-methyl-1,3,4-thiadiazol-2-yl)azetidine-3-carboxamide
  • 4-[2-(4-Chlorophenyl)-5-methylpyrazol-3-yl]piperidine
  • 1-(6-(1H-pyrazol-1-yl)pyrimidin-4-yl)-N-(4-(furan-2-yl)thiazol-2-yl)azetidine-3-carboxamide
  • N-(3-methanesulfonamidophenyl)-1-[6-(1H-pyrazol-1-yl)pyrimidin-4-yl]azetidine-3-carboxamide
  • 1-(6-(1H-pyrazol-1-yl)pyrimidin-4-yl)-N-(2-(3,5-dimethyl-1H-pyrazol-1-yl)ethyl)azetidine-3-carboxamide
  • 1-(6-(1H-pyrazol-1-yl)pyrimidin-4-yl)-N-(quinolin-8-yl)azetidine-3-carboxamide
  • 1-(6-(1H-pyrazol-1-yl)pyrimidin-4-yl)-N-(3-(methylthio)phenyl)azetidine-3-carboxamide
  • 1-(4-(4-(1-(6-(1H-pyrazol-1-yl)pyrimidin-4-yl)azetidine-3-carbonyl)piperazin-1-yl)phenyl)ethanone
  • 1-(6-(1H-pyrazol-1-yl)pyrimidin-4-yl)-N-(2-(4-acetamidobenzamido)ethyl)azetidine-3-carboxamide
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