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Merck

131377

1,10-Phenanthroline

≥99%

Synonyme(s) :

o-phenanthroline

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A propos de cet article

Formule empirique (notation de Hill) :
C12H8N2
Numéro CAS:
66-71-7
Poids moléculaire :
180.21
PubChem Substance ID:
24848008
eCl@ss:
39210124
UNSPSC Code:
12352100
NACRES:
NA.22
EC Number:
200-629-2
MDL number:
MFCD00011678
Assay:
≥99%
Form:
powder

Principaux documents

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Nom du produit

1,10-Phenanthroline, ≥99%

InChI key

DGEZNRSVGBDHLK-UHFFFAOYSA-N

InChI

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

SMILES string

c1cnc2c(c1)ccc3cccnc23

assay

≥99%

form

powder

mp

114-117 °C (lit.)

Quality Level

200

Gene Information

human ... FNTA(2339)

Catégories apparentées

Application

1,10-Phenanthroline can be used as:
  • A cathode buffer layer to improve the efficiency of organic solar cells.
  • A conventional chelator to study its efficacy in Fenton′s reaction-luminol chemiluminescence system.
  • A ligand in mild, copper (II)-catalyzed cross-coupling of organoboronic acids and sulfinate salts, leading to aryl- and alkenylsulfones.
  • A versatile ligand employed in the spectrophotometric determination of metals and photocatalytic reduction of carbon dioxide.
  • A building block for metallomacrocycles.

pictograms

Skull and crossbonesEnvironment
GHS06,GHS09

signalword

Danger

hcodes

H301,H410

Hazard Classifications

Acute Tox. 3 Oral - Aquatic Acute 1 - Aquatic Chronic 1

Classe de stockage

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges

Faites votre choix parmi les versions les plus récentes :

Certificats d'analyse (COA)

Lot/Batch Number
SDBB6364
MKCV9740
SDBB1067
MKCV3595
STBL1289

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  1. Which document(s) contains shelf-life or expiration date information for a given product?

    If available for a given product, the recommended re-test date or the expiration date can be found on the Certificate of Analysis.

  2. How do I get lot-specific information or a Certificate of Analysis?

    The lot specific COA document can be found by entering the lot number above under the "Documents" section.

  3. How do I find price and availability?

    There are several ways to find pricing and availability for our products. Once you log onto our website, you will find the price and availability displayed on the product detail page. You can contact any of our Customer Sales and Service offices to receive a quote.  USA customers:  1-800-325-3010 or view local office numbers.

  4. What is the Department of Transportation shipping information for this product?

    Transportation information can be found in Section 14 of the product's (M)SDS.To access the shipping information for this material, use the link on the product detail page for the product. 

  5. What is the difference between 1,10-Phenanthroline Products 131377 and 320056?

    Product 320056 is the monohydrate form and 131377 has no specification on water content. Both can make a copper complex, since they are the same ligand.

  6. Can Product 131377, 1,10-Phenanthroline, be used for cell culture?

    Sigma-Aldrich does not have any references for the use of 1,10-phenanthroline in cell culture.

  7. What is the solubility of Product 131377, 1,10-Phenanthroline?

    1,10-Phenanthroline is soluble in methanol at 500 micrograms per mL, or in water at 3 milligrams per mL. It is also soluble in benzene and acetone.

  8. My question is not addressed here, how can I contact Technical Service for assistance?

    Ask a Scientist here.

Aswan Sci. Technol. Bull., 13, 3-3 (1992)
Catalysis by Metal Complexes, 14, 217-217 (1993)
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Neville S Ng et al.
Dalton transactions (Cambridge, England : 2003), 42(9), 3196-3209 (2012-12-13)
Copper(II) (1(Cu)-21(Cu)) and previously established experimental anticancer platinum(II) metallointercalator complexes (1(Pt)-16(Pt)) have been prepared and investigated for their antimicrobial properties. These complexes are of the general structure [M(I(L))(A(L))](2+) where I(L) represents functionalised 1,10-phenanthrolines (1(IL)-10(IL)), and A(L) represents 1,2-diaminoethane, 1S,2S- or
Savo Lazic et al.
Photochemistry and photobiology, 93(5), 1248-1258 (2017-04-04)
Cancer remains a major global malaise requiring the advent of new, efficient and low-cost treatments. Photodynamic therapy, which combines a photosensitizer and photons to produce cytotoxic reactive oxygen species, has been established as an effective cancer treatment but has yet
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