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About This Item
Linear Formula:
FeCl3 · 6H2O
CAS Number:
Molecular Weight:
270.30
UNSPSC Code:
12352302
PubChem Substance ID:
EC Number:
231-729-4
MDL number:
Assay:
≥99.0%
Grade:
JIS special grade
Form:
solid
InChI key
NQXWGWZJXJUMQB-UHFFFAOYSA-K
InChI
1S/3ClH.Fe.6H2O/h3*1H;;6*1H2/q;;;+3;;;;;;/p-3
SMILES string
O.O.O.O.O.O.Cl[Fe](Cl)Cl
grade
JIS special grade
vapor pressure
1 mmHg ( 194 °C)
assay
≥99.0%
form
solid
reaction suitability
reagent type: catalyst
core: iron
availability
available only in Japan
bp
280-285 °C (lit.)
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signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Dam. 1 - Skin Irrit. 2
Storage Class
13 - Non Combustible Solids
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
Regulatory Information
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Sanjay Kashyap et al.
ACS nano, 8(9), 9097-9106 (2014-08-28)
Biomineralization proteins are widely used as templating agents in biomimetic synthesis of a variety of organic-inorganic nanostructures. However, the role of the protein in controlling the nucleation and growth of biomimetic particles is not well understood, because the mechanism of
D C Florian Wieland et al.
Colloids and surfaces. B, Biointerfaces, 109, 74-81 (2013-04-27)
The early stages of the formation of inorganic aggregates, composed of iron compounds at the solution-air interface, were investigated in situ. The properties of the solution-air interface were changed by using different Langmuir layers. In order to get insight into
Dattatraya H Dethe et al.
Organic letters, 15(3), 429-431 (2013-01-16)
A novel approach was developed for the synthesis of highly substituted indene derivatives, using an FeCl(3) catalyzed Prins-type cyclization reaction which was further applied in the total synthesis of jungianol and epi-jungianol.
Justin D Barr et al.
Blood, 121(18), 3733-3741 (2013-01-25)
Application of ferric chloride (FeCl(3)) to exposed blood vessels is widely used to initiate thrombosis in laboratory mice. Because the mechanisms by which FeCl(3) induces endothelial injury and subsequent thrombus formation are little understood, we used scanning electron and brightfield
Xiaoqing Li et al.
The Journal of organic chemistry, 78(18), 9499-9504 (2013-08-28)
Halosulfonylation of terminal alkynes was achieved with sulfonylhydrazides as the sulfonyl precursor and inexpensive iron halide as halide source in the presence of TBHP, allowing the regio- and stereoselective generation of (E)-β-chloro and bromo vinylsulfones.
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