552798
Gallium(III) chloride solution
0.5 M in pentane
Synonym(s):
Gallium chloride, Gallium trichloride, Trichlorogallium
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About This Item
Linear Formula:
GaCl3
CAS Number:
Molecular Weight:
176.08
MDL number:
UNSPSC Code:
12352302
PubChem Substance ID:
NACRES:
NA.23
Recommended Products
form
liquid
reaction suitability
reagent type: catalyst
core: gallium
concentration
0.5 M in pentane
bp
35 °C
density
0.688 g/mL at 25 °C
SMILES string
Cl[Ga](Cl)Cl
InChI
1S/3ClH.Ga/h3*1H;/q;;;+3/p-3
InChI key
UPWPDUACHOATKO-UHFFFAOYSA-K
signalword
Danger
hcodes
Hazard Classifications
Aquatic Chronic 2 - Asp. Tox. 1 - Eye Dam. 1 - Flam. Liq. 1 - Skin Corr. 1B - STOT SE 3
target_organs
Central nervous system
supp_hazards
Storage Class
3 - Flammable liquids
wgk_germany
WGK 3
flash_point_f
<-26.0 °F - closed cup
flash_point_c
< -32.2 °C - closed cup
ppe
Faceshields, Gloves, Goggles
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Acute and chronic effects of gallium chloride (GaCl3) on tilapia (Oreochromis mossambicus) larvae.
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Gallium is commonly used in the semiconductor industry and medical field. Biologically, gallium is able to interrupt iron metabolism. Exposure to gallium has been shown to affect the human immune system. The purpose of this study was to investigate the
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[(18)F]-FDG is a widely used tracer for the non-invasive evaluation of hypermetabolic processes like cancer and inflammation. However, [(18)F]-FDG is considered inaccurate for the diagnosis of urinary tract and genital infections because of its urinary excretion. Since the 1970s, Gallium
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Anti-cancer drugs, 10(5), 477-488 (1999-09-07)
Gallium chloride (GaCl3), an antitumor agent with antagonistic action on iron, magnesium and calcium, was tested for its ability to alter the polymerization of purified tubulin (2.2 mg/ml) in a cell-free system in vitro. GaCl3 (250 microM) does not mimic
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The Journal of organic chemistry, 72(3), 787-792 (2007-01-27)
The In(OAc)3-catalyzed reaction of bromo- and iodoalkanes with PhSiH3 in THF at 70 degrees C gave dehalogenated alkanes in good to high yields. In the presence of Et3B and air, the reduction proceeded smoothly at 30 degrees C. When 2,6-lutidine
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