514381
氯化钛(III)
≥99.995% trace metals basis
别名:
三氯化钛
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关于此项目
线性分子式:
TiCl3
化学文摘社编号:
分子量:
154.23
UNSPSC Code:
26111700
PubChem Substance ID:
EC Number:
231-728-9
MDL number:
InChI key
YONPGGFAJWQGJC-UHFFFAOYSA-K
InChI
1S/3ClH.Ti/h3*1H;/q;;;+3/p-3
SMILES string
Cl[Ti](Cl)Cl
assay
≥99.995% trace metals basis
form
crystalline
reaction suitability
reagent type: catalyst
core: titanium
mp
440 °C (dec.) (lit.)
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Application
用于气相形成具有超细粒度的金属间化合物。
signalword
Danger
hcodes
Hazard Classifications
Pyr. Sol. 1 - Skin Corr. 1B
supp_hazards
存储类别
4.2 - Pyrophoric and self-heating hazardous materials
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
法规信息
新产品
此项目有
Gnana S Siluvai et al.
Biochemistry, 48(51), 12133-12144 (2009-11-20)
Sco-like proteins contain copper bound by two cysteines and a histidine residue. Although their function is still incompletely understood, there is a clear involvement with the assembly of cytochrome oxidases that contain the Cu(A) center in subunit 2, possibly mediating
C Noubactep et al.
Journal of hazardous materials, 132(2-3), 202-212 (2005-11-08)
The effectiveness of elemental iron (Fe(0)) to remove uranium (U) from the aqueous phase has been demonstrated. While the mitigation effect is sure, discrepancies in the removal mechanism have been reported. The objective of this study was to investigate the
Catalytic oxidation of hydrazo derivatives promoted by a TiCl3/HBr system.
Eyal Drug et al.
Journal of the American Chemical Society, 129(45), 13784-13785 (2007-10-26)
D J Kushner et al.
Analytical biochemistry, 133(1), 116-119 (1983-08-01)
Hydroxamic acid siderophores were observed to be inactivated by exposure to titanium(III) chloride. To study the reaction, a series of eight model hydroxamic acids were prepared and reacted with titanium(III) chloride. The products were shown by ir and NMR comparisons
Yan Zhang et al.
Organic & biomolecular chemistry, 9(13), 4977-4982 (2011-05-21)
N-N bond cleavage in hydrazines is widely used in the preparation of amines and thus occupies a significant place in organic synthesis. In this paper, we report a new method for the reductive cleavage of N-N bonds in hydrazines by
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