552798
三氯化镓 溶液
0.5 M in pentane
别名:
Gallium chloride, Gallium trichloride, Trichlorogallium
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关于此项目
线性分子式:
GaCl3
化学文摘社编号:
分子量:
176.08
NACRES:
NA.23
PubChem Substance ID:
UNSPSC Code:
12352302
MDL number:
InChI
1S/3ClH.Ga/h3*1H;/q;;;+3/p-3
SMILES string
Cl[Ga](Cl)Cl
InChI key
UPWPDUACHOATKO-UHFFFAOYSA-K
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
signalword
Danger
target_organs
Central nervous system
supp_hazards
存储类别
3 - Flammable liquids
wgk
WGK 3
flash_point_f
<-26.0 °F - closed cup
flash_point_c
< -32.2 °C - closed cup
ppe
Faceshields, Gloves, Goggles
Hazard Classifications
Aquatic Chronic 2 - Asp. Tox. 1 - Eye Dam. 1 - Flam. Liq. 1 - Met. Corr. 1 - Skin Corr. 1B - STOT SE 3
法规信息
危险化学品
此项目有
Acute and chronic effects of gallium chloride (GaCl3) on tilapia (Oreochromis mossambicus) larvae.
H C Lin et al.
Bulletin of environmental contamination and toxicology, 60(6), 931-935 (1998-06-12)
Cristina Nanni et al.
Clinical physiology and functional imaging, 29(3), 187-192 (2009-03-27)
[(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
E M Perchellet et al.
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
Kee-Lung Chang et al.
Toxicology and applied pharmacology, 193(2), 209-217 (2003-12-03)
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
Katsukiyo Miura et al.
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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