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250198

Sigma-Aldrich

Methyl Red

ACS reagent, crystalline

Synonym(s):

2-(4-Dimethylaminophenylazo)benzoic acid, 4-Dimethylaminoazobenzene-2′-carboxylic acid, Acid Red 2

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100 ML
₹5,808.00

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100 ML
₹5,808.00

About This Item

Linear Formula:
(CH3)2NC6H4N=NC6H4CO2H
CAS Number:
Molecular Weight:
269.30
Colour Index Number:
13020
Beilstein/REAXYS Number:
750102
EC Number:
MDL number:
UNSPSC Code:
12171500
PubChem Substance ID:
NACRES:
NA.47

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grade

ACS reagent

Quality Level

form

crystalline

technique(s)

titration: suitable

visual transition interval

4.2-6.2, pink to yellow

mp

179-182 °C (lit.)

solubility

ethanol: 1 mg/mL

λmax

410 nm

application(s)

diagnostic assay manufacturing
hematology
histology

storage temp.

room temp

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1 of 4

This Item
900665333786751073
assay

≥90% (CP)

assay

≥98% (CP)

assay

≥98% (CP)

assay

98% (CP)

technique(s)

mass spectrometry (MS): suitable

technique(s)

mass spectrometry (MS): suitable

technique(s)

mass spectrometry (MS): suitable

technique(s)

mass spectrometry (MS): suitable

mass shift

M+3

mass shift

M+3

mass shift

M+3

mass shift

M+3

isotopic purity

≥95 atom % D

isotopic purity

≥98 atom % D

isotopic purity

≥98 atom % D

isotopic purity

98 atom % D

form

powder

form

powder

form

powder

form

powder

storage temp.

−20°C

storage temp.

2-8°C

storage temp.

2-8°C

storage temp.

−20°C

Application

Methyl Red has been used as pH indicator in a glucose biosensor, which is used for salivary analysis.[1]

Biochem/physiol Actions

Methyl Red is a maroon red crystal azo dye.[2] Methyl Red is a pH indicator and changes color at a pH of 5.5.[3] Methyl Red is widely used in saliva sampling method. In addition, it is also employed in carbohydrate and lactic acid detection.[2] Methyl Red has been effectively used for intrageneric differentiation of Enterobacteriaceae.[4]

Storage Class

11 - Combustible Solids

wgk_germany

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


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J D Metzger
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Field pennycress (Thlaspi arvense L.) is a winter annual weed with a cold requirement for stem elongation and flowering. The relative abilities of several native gibberellins (GAs) and GA-precursors to elicit stem growth were compared. Of the eight compounds tested
C
Sittig's Handbook of Pesticides and Agricultural Chemicals, 91-195 (2015)
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Petiole growth in Thlaspi arvense L. was stimulated when a basic 8 hour photoperiod (4.20 milliwatts per square centimeter) was extended with low intensity light (0.16 milliwatt per square centimeter) from incandescent lamps. The day length extension was effective only
Nadjimov et al.
Journal of plant growth regulation, 18(1), 45-48 (1999-11-30)
The round-leafed mutant cotton line L-501 developed fasciation of the upper stem when field grown in Central Asia. Fasciation co-segregated with the mutant gene for round leaves In.(l) Fasciation developed at the flowering stage, but removal of floral buds did
Yan-Dong Wang et al.
Biotechnology and applied biochemistry, 37(Pt 1), 39-43 (2003-02-13)
Some metabolic inhibitors, mevastatin (MVS), chlorocholine chloride (CCC), sodium pyrophosphate (NaPP) and D,L-glyceraldehyde (DLG), were respectively added into the suspension cultures of the yew Taxus chinensis var. mairei at the late phase of cell growth to study isopentenyl pyrophosphate (IPP)

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