Weight | 172.276 g/mol |
---|---|
Formula | C8H20N4 |
Hydrogen Acceptors | 4 |
Hydrogen Donors | 4 |
Aromatic Rings | 0 |
Rotatable Bonds | 0 |
1,4,7,10-Tetraazacyclododecane (294-90-6)
Score:
#5290 in Chemistry
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- Thermodynamic study of lanthanide complexes of 1,4,7-triazacyclononane-N,N,N-triacetic acid and 1,4,7,10-tetraazacyclododecane-N,N,N,N-tetraacetic acid (Inorganic Chemistry, 1987)
- A Tris(ZnII1,4,7,10-tetraazacyclododecane) Complex as a New Receptor for Phosphate Dianions in Aqueous Solution (Journal of the American Chemical Society, 1997)
- A Novel Biomimetic Zinc(II)Fluorophore, DansylamidoethylPendant Macrocyclic Tetraamine 1,4,7,10-Tetraazacyclododecane (Cyclen) (Journal of the American Chemical Society, 1996)
- Crystal and molecular structure of sodium aqua(1,4,7,10-tetraazacyclododecane-1,4,7,10-tetraacetato)europate(III) tetrahydrate Na+(EuDOTA.H2O)-.4H2O, and its relevance to NMR studies of the conformational behavior of the lanthanide complexes formed by the macrocyclic ligand DOTA (Inorganic Chemistry, 1984)
- NOVEL MULTIPOINT MOLECULAR RECOGNITION OF NUCLEOBASES BY A NEW ZINC(II) COMPLEX OF ACRIDINE-PENDANT CYCLEN (CYCLEN = 1,4,7,10-TETRAAZACYCLODODECANE) (Journal of the American Chemical Society, 1994)
- The peptide way to macrocyclic bifunctional chelating agents: synthesis of 2-(p-nitrobenzyl)-1,4,7,10-tetraazacyclododecane-N,N',N",N'''-tetraacetic acid and study of its yttrium(III) complex. (Journal of the American Chemical Society, 1988)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - H302: Harmful if swallowed
Warning Acute toxicity, oral - Category 4 - H314: Causes severe skin burns and eye damage
Danger Skin corrosion/irritation - Category 1A, B, C - H410: Very toxic to aquatic life with long lasting effects
Warning Hazardous to the aquatic environment, long-term hazard - Category 1 -
SMILESC1CNCCNCCNCCN1
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InChIKeyQBPPRVHXOZRESW-UHFFFAOYSA-N
- Pubchem - 1,4,7,10-Tetraazacyclododecane
- Wikipedia - Cyclen
Cyclen or 1,4,7,10-tetraazacyclododecane is a macrocycle and the aza analogue of the crown ether 12-crown-4. Derivatives of cyclen are larger cyclic polyamines but the repeating unit (ethyleneimine, CH2CH2NH) is always the same. Like crown ethers, cyclen compounds are capable of selectively binding cations.
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