5-Nitro-1,10-phenanthroline

Modify Date: 2024-01-02 20:18:46

5-Nitro-1,10-phenanthroline Structure
5-Nitro-1,10-phenanthroline structure
Common Name 5-Nitro-1,10-phenanthroline
CAS Number 4199-88-6 Molecular Weight 225.203
Density 1.4±0.1 g/cm3 Boiling Point 444.0±30.0 °C at 760 mmHg
Molecular Formula C12H7N3O2 Melting Point 202-204 °C(lit.)
MSDS Chinese USA Flash Point 222.3±24.6 °C
Symbol GHS07
GHS07
Signal Word Warning

 Use of 5-Nitro-1,10-phenanthroline


5-Nitro-1,10-phenanthroline (5-NP), is a o-Phenanthroline (HY-W004544) derivative, as a mediator of glucose oxidase (GOX) with antituberculous activity. 5-Nitro-1,10-phenanthroline can be applied as redox mediators for oxidases and is suitable for the development of reagent-less biosensors and biofuel cells[1][1].

 Names

Name 5-Nitro-1,10-phenanthroline
Synonym More Synonyms

 5-Nitro-1,10-phenanthroline Biological Activity

Description 5-Nitro-1,10-phenanthroline (5-NP), is a o-Phenanthroline (HY-W004544) derivative, as a mediator of glucose oxidase (GOX) with antituberculous activity. 5-Nitro-1,10-phenanthroline can be applied as redox mediators for oxidases and is suitable for the development of reagent-less biosensors and biofuel cells[1][1].
Related Catalog
In Vitro 5-Nitro-1,10-phenanthroline (25 μM; 24 h) kills naturally resistant intracellular bacteria by inducing autophagy in THP-1 macrophages[2]. 5-Nitro-1,10-phenanthroline (1x, 5x, 20x or 50x MIC, MIC=0.78 μM; 1 h) also modulates the host machinery to kill intracellular pathogens by inhibiting mycolic acid biosynthesis of Mtb[2]. Cell Viability Assay[2] Cell Line: Mtb H37Rv, M. bovis BCG and M. bovis BCG-5NP resistant strain Concentration: 0-12.5 μM Incubation Time: 24 hours Result: Inhibited pathogens with MIC99 values of 0.78 μM (Mtb H37Rv), 0.78 μM (M. bovis BCG), and >12.5 μM (M. bovis BCG-5NP), respectively.

 Chemical & Physical Properties

Density 1.4±0.1 g/cm3
Boiling Point 444.0±30.0 °C at 760 mmHg
Melting Point 202-204 °C(lit.)
Molecular Formula C12H7N3O2
Molecular Weight 225.203
Flash Point 222.3±24.6 °C
Exact Mass 225.053833
PSA 71.60000
LogP 1.56
Vapour Pressure 0.0±1.0 mmHg at 25°C
Index of Refraction 1.768
Water Solubility insoluble

 Safety Information

Symbol GHS07
GHS07
Signal Word Warning
Hazard Statements H315-H319-H335
Precautionary Statements P261-P305 + P351 + P338
Personal Protective Equipment dust mask type N95 (US);Eyeshields;Gloves
Hazard Codes Xn: Harmful;Xi: Irritant;
Risk Phrases R36/37/38
Safety Phrases S26-S36-S24/25
RIDADR NONH for all modes of transport
WGK Germany 3
HS Code 2933990090

 Synthetic Route

~98%

5-Nitro-1,10-phenanthroline Structure

5-Nitro-1,10-ph...

CAS#:4199-88-6

Literature: Ji, Shaomin; Guo, Huimin; Yuan, Xiaolin; Li, Xiaohuan; Ding, Haidong; Gao, Peng; Zhao, Chunxia; Wu, Wenting; Wu, Wanhua; Zhao, Jianzhang Organic Letters, 2010 , vol. 12, # 12 p. 2876 - 2879

~42%

5-Nitro-1,10-phenanthroline Structure

5-Nitro-1,10-ph...

CAS#:4199-88-6

Literature: Nisshinbo Industries, Inc. Patent: US5856479 A1, 1999 ;

~0%

5-Nitro-1,10-phenanthroline Structure

5-Nitro-1,10-ph...

CAS#:4199-88-6

Literature: Amouyal, Edmond; Homsi, Abdulrazzak; Chambron, Jean-Claude; Sauvage, Jean-Pierre Journal of the Chemical Society, Dalton Transactions: Inorganic Chemistry (1972-1999), 1990 , # 6 p. 1841 - 1845

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5-Nitro-1,10-phenanthroline Structure

5-Nitro-1,10-ph...

CAS#:4199-88-6

Literature: Halcrow; Kermack Journal of the Chemical Society, 1946 , p. 155

~%

5-Nitro-1,10-phenanthroline Structure

5-Nitro-1,10-ph...

CAS#:4199-88-6

Literature: Halcrow; Kermack Journal of the Chemical Society, 1946 , p. 155

~%

Detail
Literature: Inglett; Smith Journal of the American Chemical Society, 1950 , vol. 72, p. 842

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Detail
Literature: Smith; Cagle Journal of Organic Chemistry, 1947 , vol. 12, p. 781,782

 Customs

HS Code 2933990090
Summary 2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

 Articles1

More Articles
The effect of ancillary ligand chirality and phenanthroline functional group substitution on the cytotoxicity of platinum(II)-based metallointercalators.

J. Inorg. Biochem. 101 , 1049-1058, (2007)

Fifteen platinum(II)-based metallointercalators have been synthesised that utilise substituted 1,10-phenanthroline (phen) ligands, including 5-chloro-1,10-phenanthroline (5-Cl-phen), 5-methyl-1,10-phe...

 Synonyms

5-nitro-1,10-phenenthroline
1,10-Phenanthroline, 5-nitro-
5-Nitro-1,10-phenanthroline
5-Nitro-1,10-diazaphenanthrene
EINECS 224-097-6
5-nitro-1,10-phenantroline
1,10-Phenanthroline,5-nitro
Nitroferroin
MFCD00004981