N,N,N′,N′-Tetrakis(2-pyridylmethyl)ethylenediamine
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N,N,N′,N′-Tetrakis(2-pyridylmethyl)ethylenediamine
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CAS No:
16858-02-9
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Formula:
C26H28N6
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Chemical Name:
N,N,N′,N′-Tetrakis(2-pyridylmethyl)ethylenediamine
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Synonyms:
1,2-Ethanediamine,N,N,N′,N′-tetrakis(2-pyridinylmethyl)-;Pyridine,2,2′,2′′,2′′′-[ethylenebis(nitrilodimethylene)]tetra-;N,N,N′,N′-Tetrakis(2-pyridinylmethyl)-1,2-ethanediamine;N,N,N′,N′-Tetrakis(2-pyridylmethyl)-1,2-ethanediamine;TPEN;N,N,N′,N′-Tetrakis(2-pyridylmethyl)ethylenediamine;N,N,N′,N′-Tetrakis(pyridin-2-yl-methyl)ethylenediamine;TPEDA;N,N,N′,N′-Tetra[(2-pyridyl)methyl] ethylenediamine;166984-59-4
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CAS No:
Description
Colourless CrystalsChEBI: An N-substituted diamine that is ethylenediamine in which the four amino hydrogens are replaced by 2-pyridylmethyl groups.
N,N,N',N'-tetrakis(2-pyridylmethyl)ethylenediamine is an N-substituted diamine that is ethylenediamine in which the four amino hydrogens are replaced by 2-pyridylmethyl groups. It has a role as a chelator, an apoptosis inducer and a copper chelator. It is a member of pyridines, a tertiary amino compound and a N-substituted diamine. It derives from an ethylenediamine.
N,N,N′,N′-Tetrakis(2-pyridylmethyl)ethylenediamine Basic Attributes
424.54
424.54
R9PTU1U29I
DTXSID50168583
29333990
Characteristics
58
2.1
White crystalline powder
1.3893 (rough estimate)
110.50-111.00 °C @ Solvent: Ethyl acetate, Hexane
530.56°C (rough estimate)
281.7±28.7 °C
1.4570 (estimate)
Refrigerator
8.14E-12mmHg at 25°C
Safety Information
NONH for all modes of transport
3
36/37/38
26-36
Xi
P261-P305 + P351 + P338
H315-H319-H335
|Warning|H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]|P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, and P501|Aggregated GHS information provided by 195 companies from 3 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
Drug Information
Chemicals that bind to and remove ions from solutions. Many chelating agents function through the formation of COORDINATION COMPLEXES with METALS. (See all compounds classified as Chelating Agents.)|Drugs that inhibit cholinesterases. The neurotransmitter ACETYLCHOLINE is rapidly hydrolyzed, and thereby inactivated, by cholinesterases. When cholinesterases are inhibited, the action of endogenously released acetylcholine at cholinergic synapses is potentiated. Cholinesterase inhibitors are widely used clinically for their potentiation of cholinergic inputs to the gastrointestinal tract and urinary bladder, the eye, and skeletal muscles; they are also used for their effects on the heart and the central nervous system. (See all compounds classified as Cholinesterase Inhibitors.)
N,N,N',N'-tetrakis(2-pyridylmethyl)ethylenediamine
N,N,N′,N′-Tetrakis(2-pyridylmethyl)ethylenediamine Use and Manufacturing
Membrane-permeable zinc chelator; decreased the intracellular level of zinc and induced apoptosis
Computed Properties
Molecular Weight:424.5
XLogP3:2.1
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:11
Exact Mass:424.23754492
Monoisotopic Mass:424.23754492
Topological Polar Surface Area:58
Heavy Atom Count:32
Complexity:419
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes
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N,N,N′,N′-Tetrakis(2-pyridylmethyl)ethylenediamine
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