Key Documents

View All Documentation

301868

4,7-Phenanthroline

Name: 4,7-Phenanthroline
Brand: ALDRICH

98%

Select a Size

Change View

About This Item

Empirical Formula (Hill Notation):

C₁₂H₈N₂

CAS Number:

230-07-9

Molecular Weight:

180.21

NACRES:

NA.22

PubChem Substance ID:

24858214

UNSPSC Code:

12352100

MDL number:

MFCD00004987

Assay:

98%

Technical Service

Need help? Our team of experienced scientists is here for you.

Let Us Assist

Properties

assay

98%

mp

172-174 °C (lit.)

SMILES string

c1cnc2ccc3ncccc3c2c1

InChI

1S/C12H8N2/c1-3-9-10-4-2-8-14-12(10)6-5-11(9)13-7-1/h1-8H

InChI key

DATYUTWESAKQQM-UHFFFAOYSA-N

Description

General description

4,7-Phenanthroline reacts with ruthenium carbonyl to yield cyclometalated derivatives.

Application

4,7-Phenanthroline was used in preparation of:

cyclic tetranuclear half-sandwich ruthenium(II) complexes
positively charged homochiral cyclic trinuclear metallacalix[3]arene species

pictograms

GHS05,GHS07

signalword

Danger

hcodes

H302,H318

pcodes

P264 - P270 - P280 - P301 + P312 - P305 + P351 + P338 - P501

Hazard Classifications

Acute Tox. 4 Oral - Eye Dam. 1

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Reactions of phthalazine, quinazoline, 4,7-phenanthroline and 2,3'-bipyridine with ruthenium carbonyl.

Javier A Cabeza et al.

Dalton transactions (Cambridge, England : 2003), 41(24), 7249-7257 (2012-05-10)

The reactions of [Ru(3)(CO)(12)] with four aromatic diazines have been studied in THF at reflux temperature. With phthalazine (L(1)), the compound [Ru(3)(μ-κ(2)N(2)N(3)-L(1))(μ-CO)(3)(CO)(7)] (1), which contains an intact phthalazine ligand in an axial position bridging an Ru-Ru edge through both N

Regulation of glucose transport in the NIH 3T3 L1 preadipocyte cell line by TCDD.

H Olsen et al.

Environmental health perspectives, 102(5), 454-458 (1994-05-01)

This study examined the changes in cellular glucose uptake induced by 2,3,7,8 tetrachlorodibenzo-p-dioxin (TCDD) as measured by quantification of intracellular radioactivity in the NIH 3T3 L1 preadipocyte cell line after a 30-minute incubation with the non-metabolizable radioactive analogue of glucose

2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) modulates function of human luteinizing granulosa cells via cAMP signaling and early reduction of glucose transporting activity.

E Enan et al.

Reproductive toxicology (Elmsford, N.Y.), 10(3), 191-198 (1996-05-01)

This study examined the changes in cellular glucose uptake, cAMP-dependent protein kinase (PKA), and progesterone production induced by 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) in human luteinizing granulosa cells (LGCs) in culture. The role of Ah receptor on TCDD-mediated toxicity in human LGCs was

View All Related Papers

Global Trade Item Number

SKU	GTIN
301868-1G	04061826238943