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Merck

202096

Sigma-Aldrich

Neues Methylenblau N Hemi-(zinkchlorid) (Salz)

Dye content 90 %

Synonym(e):

Methylenblau N Hemi-(zinkchlorid) (Salz), Rhodulinreinblau 24

Anmeldenzur Ansicht organisationsspezifischer und vertraglich vereinbarter Preise


About This Item

Empirische Formel (Hill-System):
C18H22ClN3S · 0.5ZnCl2
CAS-Nummer:
Molekulargewicht:
416.05
Farbindexnummer:
52030
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
12171500
PubChem Substanz-ID:
NACRES:
NA.47

Form

powder

Zusammensetzung

Dye content, 90%

mp (Schmelzpunkt)

>240 °C (dec.) (lit.)

λmax

591 nm
630 nm (2nd)

ε (Extinktionskoeffizient)

≥16000 at 242-248 nm in H2O
≥28000 at 284-290 nm in H2O
≥36000 at 588-594 nm in H2O
≥44000 at 629-635 nm in H2O

Anwendung(en)

diagnostic assay manufacturing
hematology
histology

Lagertemp.

room temp

SMILES String

[Cl-].[Cl-].[Cl-].[Cl-].Cl[Zn]Cl.CCNc1cc2[s+]c3cc(NCC)c(C)cc3nc2cc1C.CCNc4cc5[s+]c6cc(NCC)c(C)cc6nc5cc4C

InChI

1S/2C18H22N3S.4ClH.Zn/c2*1-5-19-13-9-17-15(7-11(13)3)21-16-8-12(4)14(20-6-2)10-18(16)22-17;;;;;/h2*7-10,19-20H,5-6H2,1-4H3;4*1H;/q2*+1;;;;;+2/p-4

InChIKey

MCBJJSJOIVJYQY-UHFFFAOYSA-J

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Anwendung

New Methylene Blue N zinc chloride double salt has been used as a photosensitizer for the in vitro photodynamic inactivation of plant-pathogenic fungi Colletotrichum acutatum and Colletotrichum gloeosporioides. It has also been used to determine the in vitro susceptibilities of Trichophyton mentagrophytes and Trichophyton rubrum microconidia to photodynamic antimicrobial chemotherapy (PACT).

Biochem./physiol. Wirkung

New Methylene Blue N zinc chloride double salt also known as methylene blue N is an azo dye. It can bind, neutralize and crosslink with RNA. This causes co-precipitation of ribosomal and residual RNA with the mitochondria and ferritin masses. These events make the living, young erythrocytes as microscopically visible, dark-blue clusters and filaments, referred to as reticulum. New Methylene Blue N zinc chloride double salt helps in counting of reticulocytes (erythrocytes containing RNA).

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

dust mask type N95 (US), Eyeshields, Gloves


Analysenzertifikate (COA)

Suchen Sie nach Analysenzertifikate (COA), indem Sie die Lot-/Chargennummer des Produkts eingeben. Lot- und Chargennummern sind auf dem Produktetikett hinter den Wörtern ‘Lot’ oder ‘Batch’ (Lot oder Charge) zu finden.

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In der Dokumentenbibliothek finden Sie die Dokumentation zu den Produkten, die Sie kürzlich erworben haben.

Die Dokumentenbibliothek aufrufen

Mary Turgeon
Linne & Ringsrud's Clinical Laboratory Science (2011)
In Vitro Photodynamic Inactivation of Plant-Pathogenic Fungi Colletotrichum acutatum and Colletotrichum gloeosporioides with Novel Phenothiazinium Photosensitizers
de Menezes HD
Applied and Environmental Microbiology, 80, 1623-1632 (2014)
Susceptibilities of the dermatophytes Trichophyton mentagrophytes and T. rubrum microconidia to photodynamic antimicrobial chemotherapy with novel phenothiazinium photosensitizers and red light
Rodrigues GB
Journal of Photochemistry and Photobiology. B, Biology, 89-94 (2012)
PHOTODEGRADATION OF NEW METHYLENE BLUE N IN
AQUEOUS SOLUTION USING ZINC OXIDE AND
TITANIUM DIOXIDE AS CATALYST
ALI R
Jurnal Teknologi, 45, 31-42 (2006)
Gabriela Braga Rodrigues et al.
Journal of photochemistry and photobiology. B, Biology, 209, 111942-111942 (2020-07-06)
Antimicrobial photodynamic treatment (APDT) has emerged as an effective therapy against pathogenic fungi with both acquired and intrinsic resistance to commonly used antifungal agents. Success of APDT depends on the availability of effective photosensitizers capable of acting on different fungal

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