447862
Bis(butylcyclopentadienyl)zirconium(IV) dichloride
97%
Synonym(s):
Dibutylzirconocene dichloride
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About This Item
Empirical Formula (Hill Notation):
C18H26Cl2Zr
CAS Number:
Molecular Weight:
404.53
MDL number:
UNSPSC Code:
12161600
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
Quality Level
Assay
97%
form
solid
reaction suitability
core: zirconium
reagent type: catalyst
reaction type: Olefin Metathesis
mp
98.7-99.4 °C (lit.)
SMILES string
Cl[Zr]Cl.CCCC[C]1[CH][CH][CH][CH]1.CCCC[C]2[CH][CH][CH][CH]2
InChI
1S/2C9H13.2ClH.Zr/c2*1-2-3-6-9-7-4-5-8-9;;;/h2*4-5,7-8H,2-3,6H2,1H3;2*1H;/q;;;;+2/p-2
InChI key
KZUKCLOWAMFDDB-UHFFFAOYSA-L
Related Categories
Application
Catalyst for:
Metallocene supported catalyst
- Copolymerization of ethylene-alpha-olefin
- Ethylene polymerization
Metallocene supported catalyst
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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T C Tallant et al.
Journal of bacteriology, 179(22), 6902-6911 (1997-11-26)
During growth on acetate, Methanosarcina barkeri expresses catabolic enzymes for other methanogenic substrates such as monomethylamine. The range of substrates used by cells grown on acetate was further explored, and it was found that cells grown on acetate also converted
Determination of enantiomeric purity of 3-mercapto-2-methylpropionic acid.
D Wang-Iverson et al.
Journal of chromatography, 408, 365-371 (1987-11-06)
H G Brittain et al.
Pharmaceutical research, 7(10), 1082-1085 (1990-10-01)
The ultraviolet and circular dichroism spectra of authentic captopril have been obtained, since the reported literature data are inconsistent with those obtained on highly purified material. The UV absorption spectrum consists of a single band maximum at 200 nm, while
M R Smith et al.
Bioorganic & medicinal chemistry, 2(7), 589-593 (1994-07-01)
A bacterium (strain photoB) photoassimilated 3-mercapto-2-methylpropionate as sole source of sulphur with methacrylate accumulating in the medium. This was thought to be the product of a sulphur-lyase type enzyme attacking the 3-mercapto-2-methylpropionate. Detailed examination of the biochemistry of the utilization
Erinn C Howard et al.
Science (New York, N.Y.), 314(5799), 649-652 (2006-10-28)
Flux of dimethylsulfide (DMS) from ocean surface waters is the predominant natural source of sulfur to the atmosphere and influences climate by aerosol formation. Marine bacterioplankton regulate sulfur flux by converting the precursor dimethylsulfoniopropionate (DMSP) either to DMS or to
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