C26H20N2
360.4 g/mol
Research ReagentWarning
Bathocuproine
CAS4733-39-5EC225-240-5
Category
Research Reagent
Compound Class
Heterocycle
Primary Use
Research Compound
Bathocuproine is a research reagent primarily used as a copper chelation agent. It is a nitrogen-containing heterocyclic compound with a highly aromatic structure, suitable for laboratory applications involving copper ion binding.
copper chelation reagentreagent for copper detection and analysis
Content scope: Information here supports chemical identification and industrial supply, research, and manufacturing contexts. It is not a therapeutic claim, medical advice, or drug-use instructions.
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Related Compounds
StrongSame Parent
(T-4)-Dichloro(2,9-dimethyl-4,7-diphenyl-1,10-phenanthroline-N1,N10)-Nickel
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StrongSame Parent
(Bathocuproine)NiBr2
CAS326822-02-0
research compound
ReferenceSame Category
Selenoxanthen-9-one
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research compound
ReferenceSame Category
Methyl 1H-indazole-5-carboxylate
CAS473416-12-5
research compound
ReferenceSame Category
3,5-Dibromo-2-fluoropyridine
CAS473596-07-5
research compound
ReferenceSame Category
Ethyltriphenylphosphonium iodide
CAS4736-60-1
research compound
Referencesame scaffold
Bathophenanthroline
CAS1662-01-7
Solar energy materials
Safety Reference
Warning
H302Harmful if swallowed
H413May cause long lasting harmful effects to aquatic life
Customs Tariff Classification
The international HS code for Bathocuproine (CAS 4733-39-5) is 2933.99.
HS code (international, 6-digit)
2933.99
EU CN code (8-digit)
2933 99 80
Classification per the EU customs inventory ECICS (2026-07 snapshot, HS 2022). National tariff lines and product form can affect the final classification.
Identifiers
IUPAC Name
2,9-dimethyl-4,7-diphenyl-1,10-phenanthroline
InChIKey
STTGYIUESPWXOW-UHFFFAOYSA-N
SMILES
CC1=CC(=C2C=CC3=C(C=C(N=C3C2=N1)C)C4=CC=CC=C4)C5=CC=CC=C5
Synonyms (15)
- 1, 2,9-dimethyl-4,7-diphenyl-
- Bathocuproin
- Bathocuproine
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