Hafnium(IV) chloride

Names

[ Name ]:
Hafnium(IV) chloride

[Synonym ]:
Hafnium chloride(HfCl4)
Hafnium(IV) chloride,-80 mesh
HAFNIUMANDITSCOMPOUNDS
MFCD00011034
hafnium(IV) chloride
HfCl4
EINECS 236-826-5
HAFNIUM TETRACHLORIDE

Chemical & Physical Properties

[ Boiling Point ]:
319.0ºC (sublimes)

[ Melting Point ]:
319 °C

[ Molecular Formula ]:
Cl₄Hf

[ Molecular Weight ]:
320.30200

[ Exact Mass ]:
319.82200

[ LogP ]:
2.75800

[ Vapour Pressure ]:
1 mm Hg ( 190 °C)

MSDS

Safety Information

[ Symbol ]:

GHS05

[ Signal Word ]:
Danger

[ Hazard Statements ]:
H314

[ Precautionary Statements ]:
P280-P305 + P351 + P338-P310

[ Hazard Codes ]:
C: Corrosive;

[ Risk Phrases ]:
R34

[ Safety Phrases ]:
S26-S36/37/39-S45

[ RIDADR ]:
UN 3260 8/PG 2

[ WGK Germany ]:
3

[ Packaging Group ]:
II

[ Hazard Class ]:
8

Precursor & DownStream

Precursor

DownStream

hafnium(4+),methanidylbenzene
tetrakis(dimethylamino)hafnium
Butyl methacrylate
bis(pentamethylcyclopentadienyl)hafnium dichloride
Pentamethylcyclopentadienylhafnium trichloride
Chlorotrimethylsilane
Hafnocene Dichloride
hafnium iodide
hafnium bromide
hafnium fluoride

Articles

Production of 9-hydroxynonanoic Acid from methyl oleate and conversion into lactone monomers for the synthesis of biodegradable polylactones.

Biomacromolecules 9(3) , 949-53, (2008)

The feasibility of a previously established method based on ozonolysis and hydrogenation reactions for the production of 9-hydroxynonanoic acid from oleic acid has been demonstrated. Metal catalyzed l...

Hydroaminations of unactivated alkenes with basic alkylamines: group 4 metal halide catalysts and Brønsted-acid organocatalysts.

Org. Biomol. Chem. 5(12) , 1975-8, (2007)

Two distinct economical catalysts for intramolecular hydroaminations of electronically unactivated alkenes with basic amines are described, which are based on (a) group 4 metal halides under basic rea...

Visualization of the cytoskeletal elements in tissue culture cells by bloc-staining with hafnium chloride after rapid freezing and freeze-substitution fixation.

J. Electron Microsc. (Tokyo) 33(2) , 186-90, (1984)

2-[(2-Cyanoethyl)[(prop-2-en-1-yloxy)carbonyl]amino]-2-methylpropanoic acid
7-[(Prop-2-en-1-yloxy)carbonyl]-5,6,7,8-tetrahydro-2,7-naphthyridine-4-carboxylic acid
6-[(Prop-2-en-1-yloxy)carbonyl]-5,6,7,8-tetrahydro-1,6-naphthyridine-4-carboxylic acid
2-Methyl-1-[(prop-2-en-1-yloxy)carbonyl]-1,2,3,4-tetrahydroquinoline-4-carboxylic acid
1-methyl-6-[(prop-2-en-1-yloxy)carbonyl]-1H,4H,5H,6H,7H-pyrazolo[3,4-c]pyridine-3-carboxylic acid
5-Oxo-1-{1-[(prop-2-en-1-yloxy)carbonyl]piperidin-4-yl}pyrrolidine-3-carboxylic acid
5-Benzyloxycarbonyl-1,4,6,7-tetrahydropyrazolo[4,3-C]pyridine-3-carboxylic acid
1-Methyl-5-phenylmethoxycarbonyl-6,7-dihydro-4H-pyrazolo[4,3-c]pyridine-3-carboxylic acid
2-Methyl-5-phenylmethoxycarbonyl-6,7-dihydro-4H-pyrazolo[4,3-c]pyridine-3-carboxylic acid
2-{[(Benzyloxy)carbonyl]amino}-3-hydroxy-3-(4-methoxyphenyl)propanoic acid

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