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08714

Millipore

Methyl Red solution

suitable for microbiology

Sinonimo/i:

Methyl red indicator solution

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About This Item

Formula empirica (notazione di Hill):
C15H15N3O2
Numero CAS:
493-52-7
Peso molecolare:
269.30
Beilstein:
1843037
Numero MDL:
MFCD00002425
Codice UNSPSC:
41171621
ID PubChem:
329748627
NACRES:
NA.85

agenzia

according to GB 4789.30-2016
according to ISO 22964:2017

Livello qualitativo

200

Nome Commerciale

BioChemika

Durata

limited shelf life, expiry date on the label

Composizione

dist. water, 200 mL
ethanol 95%, 300 mL
methyl red, 0.1 g

tecniche

microbe id | metabolite detection: suitable

applicazioni

clinical testing
environmental
food and beverages
microbiology

Compatibilità

Enterococcus spp.
Escherichia coli
Klebsiella spp.
Proteus spp.
Pseudomonas spp.
Staphylococcus spp.
bacteria

Stringa SMILE

CN(C)c1ccc(cc1)\N=N\c2ccccc2C(O)=O

InChI

1S/C15H15N3O2/c1-18(2)12-9-7-11(8-10-12)16-17-14-6-4-3-5-13(14)15(19)20/h3-10H,1-2H3,(H,19,20)/b17-16+
CEQFOVLGLXCDCX-WUKNDPDISA-N

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Categorie correlate

Descrizione generale

Methyl red solution is an azo dye which turns to red when pH is below 4.4 (yellow pH < 6.2, orange pH 4.4-6.2). Some bacteria utilize glucose to form large amounts of acid with the result that the pH value of the medium falls distinct. Other species produce no or less free acid. This difference can be visualized by using methyl red. This test is used to differentiate enteric bacteria.

Applicazioni

Methyl red solution is a pH indicator dye recommended for detection of bacteria producing acid from glucose fermentation such as Enterobacteriaceae in various samples.

Pittogrammi

FlameExclamation mark
GHS02,GHS07

Avvertenze

Danger

Indicazioni di pericolo

H225,H319

Classi di pericolo

Eye Irrit. 2 - Flam. Liq. 2

Codice della classe di stoccaggio

3 - Flammable liquids

Classe di pericolosità dell'acqua (WGK)

WGK 1

Punto d’infiammabilità (°F)

69.8 °F

Punto d’infiammabilità (°C)

21 °C

Dispositivi di protezione individuale

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

Choose from one of the most recent versions:

Certificati d'analisi (COA)

Lot/Batch Number
BCCL8848
BCCL0746
BCCK1481
BCCJ3868
BCCG7250

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Chan-Ju Wang et al.
Acta crystallographica. Section F, Structural biology and crystallization communications, 66(Pt 1), 2-7 (2010-01-09)
Azoreductase 1 from Pseudomonas aeruginosa strain PAO1 (paAzoR1) catalyses the activation of the prodrug balsalazide and reduces the azo dye methyl red using reduced nicotinamide adenine dinucleotide cofactor as an electron donor. To investigate the mechanism of the enzyme, a
Oana Alexandru et al.
Journal of neuro-oncology, 102(1), 9-18 (2010-07-17)
A major focus of brain cancer research today is to translate understanding of glioma biology into advances in treatment, by exploring the potential of target therapy. Here we investigated the ability of three compounds belonging to the chemical class of
Z Ioannou et al.
Water science and technology : a journal of the International Association on Water Pollution Research, 67(5), 1129-1136 (2013-02-19)
Zeolite, hematite, modified zeolite and commercial activated charcoal were examined for their ability to remove methylene blue (MB) and methyl red (MR) from their aqueous solutions. Modified zeolite and hematite were produced according to the Schwertmann and Cornell method while
Robin L Stingley et al.
Journal of medical microbiology, 59(Pt 1), 108-114 (2009-09-05)
Reduction of Methyl Red (MR) and Orange II (Or II) by 26 human skin bacterial species was monitored by a rapid spectrophotometric assay. The analysis indicated that skin bacteria, representing the genera Staphylococcus, Corynebacterium, Micrococcus, Dermacoccus and Kocuria, were able
X D Zhang et al.
Journal of hazardous materials, 170(2-3), 883-887 (2009-06-09)
An aqueous C.I. Acid Red 2 solution was decolorized by electrolysis using iron as anode. The decolorization mechanism was investigated through experimental observations on the electrochemical behavior of C.I. Acid Red 2 on Pt rotating disk electrode, UV-visible spectra of
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