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33510

Sigma-Aldrich

1,10-Phenanthroline monohydrate

redox indicator, ACS reagent, puriss. p.a., ≥99.5% (calc. to the dried substance)

Synonyme(s) :

o-Phenanthroline monohydrate

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About This Item

Formule empirique (notation de Hill):
C12H8N2 · H2O
Numéro CAS:
5144-89-8
Poids moléculaire :
198.22
Numéro Beilstein :
4008096
Numéro CE :
200-629-2
Numéro MDL:
MFCD00149973
Code UNSPSC :
12352100
ID de substance PubChem :
57648856
Nomenclature NACRES :
NA.21

product name

1,10-Phenanthroline monohydrate, ACS reagent, puriss. p.a., ≥99.5% (calc. to the dried substance), for redox titration

Qualité

ACS reagent
puriss. p.a.

Niveau de qualité

200

Pureté

≥99.5% (calc. to the dried substance)
8.5-9.5% water basis

Technique(s)

titration: suitable

Impuretés

8.5-9.5% water

Résidus de calcination

≤0.05% (as SO4)

Pf

100-104 °C (lit.)
97-102 °C

Adéquation

passes test for iron detection
passes test for redox indicator

Chaîne SMILES 

O.c1cnc2c(c1)ccc3cccnc23

InChI

1S/C12H8N2.H2O/c1-3-9-5-6-10-4-2-8-14-12(10)11(9)13-7-1;/h1-8H;1H2

Clé InChI

PPQJCISYYXZCAE-UHFFFAOYSA-N

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Description générale

1,10-Phenanthroline monohydrate is the hydrated form of o-phenanthroline.

Application

1,10-Phenanthroline monohydrate (phen) may be used in the photochemical quantification of Fe3+ and total iron in mineral samples. It may be used as starting reagent for the preparation of 5-nitro-1,10-phenanthroline.
When complexed with copper, it possesses nuclease activity that has been used to study DNA-protein interactions.

Actions biochimiques/physiologiques

Metalloprotease inhibitor; chelates iron, zinc and other divalent metals. Effective concentration 1-10 mM.

Pictogrammes

Skull and crossbonesEnvironment
GHS06,GHS09

Mention d'avertissement

Danger

Mentions de danger

H301,H410

Classification des risques

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

Code de la classe de stockage

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

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

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

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Certificats d'analyse (COA)

Lot/Batch Number
BCCL5564
BCCL8757
BCCG1840
BCCC0594
BCBX4555

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Consulter la Bibliothèque de documents

The quantitative assay of minerals for Fe2+ and Fe3+ using 1, 10-phenanthroline: II. A photochemical method.
Stucki JW.
Soil Science Society of America Journal. Soil Science Society of America, 45(3), 638-641 (1981)
A luminescent tris (2-thenoyltrifluoroacetonato) europium (III) complex covalently linked to a 1, 10-phenanthroline-functionalised sol-gel glass.
Binnemans K, et al.
Journal of Materials Chemistry, 14(2), 191-195 (2004)
Kyle R Simonetta et al.
Nature communications, 10(1), 1402-1402 (2019-03-31)
Protein-protein interactions (PPIs) governing the recognition of substrates by E3 ubiquitin ligases are critical to cellular function. There is significant therapeutic potential in the development of small molecules that modulate these interactions; however, rational design of small molecule enhancers of
Unmesh Jadhav et al.
Molecular cell, 78(1), 141-151 (2020-02-07)
Polycomb repressive complex 2 (PRC2) places H3K27me3 at developmental genes and is causally implicated in keeping bivalent genes silent. It is unclear if that silence requires minimum H3K27me3 levels and how the mark transmits faithfully across mammalian somatic cell generations.
Doo Sin Jo et al.
Autophagy, 16(11), 1989-2003 (2020-01-23)
Quality control of peroxisomes is essential for cellular homeostasis. However, the mechanism underlying pexophagy is largely unknown. In this study, we identified HSPA9 as a novel pexophagy regulator. Downregulation of HSPA9 increased macroautophagy/autophagy but decreased the number of peroxisomes in
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