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08714

Millipore

Methyl Red solution

suitable for microbiology

Synonym(s):

Methyl red indicator solution

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About This Item

Empirical Formula (Hill Notation):
C15H15N3O2
CAS Number:
493-52-7
Molecular Weight:
269.30
Beilstein:
1843037
MDL number:
MFCD00002425
UNSPSC Code:
41171621
PubChem Substance ID:
329748627
NACRES:
NA.85

Agency

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

Quality Level

200

product line

BioChemika

shelf life

limited shelf life, expiry date on the label

composition

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

technique(s)

microbe id | metabolite detection: suitable

application(s)

clinical testing
environmental
food and beverages
microbiology

suitability

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

SMILES string

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+

InChI key

CEQFOVLGLXCDCX-WUKNDPDISA-N

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General description

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.

Application

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

Pictograms

FlameExclamation mark
GHS02,GHS07

Signal Word

Danger

Hazard Statements

H225,H319

Hazard Classifications

Eye Irrit. 2 - Flam. Liq. 2

Storage Class Code

3 - Flammable liquids

WGK

WGK 1

Flash Point(F)

69.8 °F

Flash Point(C)

21 °C

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCCL8848
BCCL0746
BCCK1481
BCCJ3868
BCCG7250

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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
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
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
S S Gomare et al.
Journal of applied microbiology, 106(3), 993-1004 (2009-02-04)
To evaluate the potential of Brevibacillus laterosporus MTCC 2298 for the decolourization of different textile azo dyes including methyl red, mechanism of biotransformation and the toxicity of products. Brevibacillus laterosporus showed decolourization of thirteen different azo dyes including methyl red.
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