Cart
sales@molnova.com
Gadolinium(III) chloride hexahydrate
CAS No. 13450-84-5
Gadolinium(III) chloride hexahydrate( —— )
Catalog No. M35902 CAS No. 13450-84-5
Gadolinium(III) chloride hexahydrate is a contrast agent in magnetic resonance imaging and can be used in medicine, magnetic resonance imaging, liquid crystal displays and other fields.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 500MG | 40 | In Stock |
|
| 1G | 57 | In Stock |
|
Biological Information
-
Product NameGadolinium(III) chloride hexahydrate
-
NoteResearch use only, not for human use.
-
Brief DescriptionGadolinium(III) chloride hexahydrate is a contrast agent in magnetic resonance imaging and can be used in medicine, magnetic resonance imaging, liquid crystal displays and other fields.
-
DescriptionGadolinium(III) chloride hexahydrate is a contrast agent in magnetic resonance imaging and can be used in medicine, magnetic resonance imaging, liquid crystal displays and other fields. Gadolinium(III) chloride hexahydrate can be used to synthesize complexes and nanomaterials.
-
In Vitro——
-
In Vivo——
-
Synonyms——
-
PathwayOthers
-
TargetOther Targets
-
RecptorOthers
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number13450-84-5
-
Formula Weight371.7
-
Molecular FormulaCl3GdH12O6
-
Purity>98% (HPLC)
-
Solubility——
-
SMILESCl[Gd](Cl)Cl.O.O.O.O.O.O
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
molnova catalog
related products
-
Hippuric acid
Hippuric acid is an acyl glycine formed by the conjugation of benzoic acid with glycine. Hippuric acid is a normal component of urine and is typically increased with increased consumption of phenolic compounds (tea wine fruit juices).
-
ADAMTS-5 Inhibitor
ADAMTS-5 Inhibitor is a potent ADAMTS-5 (aggrecanase-2) inhibitor, with an IC50 of 1.1 μM. ADAMTS-5 Inhibitor shows >40-fold functional selectivity over ADAMTS-4 (aggrecanase-1).
-
CHR-6494 TFA
CHR-6494 TFA is a potent haspin inhibitor, with an?IC50?of 2 nM. It inhibits histone H3T3 phosphorylation. CHR-6494 TFA induces the?apoptosis?of cancer cells, including melanoma and breast cancer. CHR-6494 TFA can be used in the research of cancer.
