Substance
ID:368900
Names and Identifiers
IUPAC name
1,10-phenanthroline hydrate
IUPAC Traditional name
phen hydrate
Synonyms
邻菲咯啉 一水合物1,10-菲咯啉 一水合物1,10-Phenanthroline monohydrateo-Phenanthroline monohydrate
Registration numbers
EC Number
CAS Number
MDL Number
Beilstein Number
PubChem SID
Properties
Safety Information
Hazard Class
6.1
Personal Protective Equipment
Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges
GHS Precautionary statements
P273-P301+P310-P501
Safety Statements
45-60-61
GHS Hazard statements
H301-H410
GHS Pictograms
Hazardous to the aquatic environment
Acute hazard, category1
Chronic hazard, categories 1,2
Acute toxicity (oral, dermal, inhalation), categories 1,2,3
Packing Group
3
German water hazard class
3
GHS Signal Word
Danger
RID/ADR
UN 2811 6.1/PG 3
Risk Statements
25-50/53
European Hazard Symbols
Nature polluting (N)
Toxic (T)MSDS Link
UN Number
2811
RTECS
SF8300000
Product Information
Grade
ACS reagent
puriss. p.a.
Empirical Formula (Hill Notation)
C12H8N2 · H2O
Purity
8.5-9.5% water basis
≥99.5% (calc. to the dried substance)
Ignition Residue
≤0.05% (as SO4)
Suitability
passes test for redox indicator
passes test for iron detection
Physical Property
Melting Point
117-120 °C (ex dried substance)
100-104 °C(lit.)
Molecule Details
Application
When complexed with copper, it possesses nuclease activity that has been used to study DNA-protein interactions.
Biochem/physiol Actions
Metalloprotease inhibitor; chelates iron, zinc and other divalent metals. Effective concentration 1-10 mM.
When complexed with copper, it possesses nuclease activity that has been used to study DNA-protein interactions.
Biochem/physiol Actions
Metalloprotease inhibitor; chelates iron, zinc and other divalent metals. Effective concentration 1-10 mM.
Molecular Spectra
No Data Available
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References
No Data Available
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