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Thiazolyl Blue

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Thiazolyl Blue Basic information

Product Name:
Thiazolyl Blue
Synonyms:
  • 2-(4,5-Dimethyl-2-thiazolyl)-3,5-diphenyl-2H-tetrazol-3-ium Bromide
  • Thiazolyl Blue Tetrazolium Bromide Vetec(TM) reagent grade, 98%
  • ACRYL/BIS 29:1 PREMIXED PWD ULTRA PURE
  • 3-(4,5-Dimethyl-2-Thiazolyl)-2,5-Diphenyl
  • 3-(4,5-Dimethylthiazol-2-yl)-2,5-diphenyl-2,3-dihydro-1H-tetrazol-3-ium bromide
  • 2-(4,5-Dimethylthiazol-2-yl)-3,5-diphenyl-2,3-dihydro-1H-tetrazol-3-ium bromide
  • 2,5-diphenyl-3-(4,5-dimethylthiazol-2-yl)-2h-tetrazolium Bromide
  • 2,5-diphenyl-3-(4,5-dimethylthiazol-2-yl)tetrazolium Bromide
CAS:
298-93-1
MF:
C18H16BrN5S
MW:
414.32
EINECS:
206-069-5
Product Categories:
  • Tetrazolium salt
  • marker
  • Tetrazolium Salts
  • Tetrazolium Salts & Formazans
  • Chemistry
Mol File:
298-93-1.mol
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Thiazolyl Blue Chemical Properties

Melting point:
195 °C (dec.) (lit.)
Density 
1.4886 (estimate)
storage temp. 
2-8°C
solubility 
methanol: 5 mg/mL, clear
form 
powder
color 
Yellow to orange
Water Solubility 
Slightly soluble.Clear yellow solution at 5mg in 1ml of water on vortexing
λmax
378 nm, 242 nm
Sensitive 
Light Sensitive
BRN 
3825277
Stability:
Hygroscopic
Biological Applications
Cell viability assay; microbial growth assays; DNA quantification assays; tissue viability assays; detecting enzymes; measuring membrane potential; treating Alzheimer’s disease,asthma,cancer
InChIKey
AZKSAVLVSZKNRD-UHFFFAOYSA-M
CAS DataBase Reference
298-93-1(CAS DataBase Reference)
EPA Substance Registry System
2H-Tetrazolium, 2-(4,5-dimethyl-2-thiazolyl)-3,5-diphenyl-, bromide (298-93-1)
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Safety Information

Hazard Codes 
Xi,T,Xn
Risk Statements 
46-68-36/37/38
Safety Statements 
22-24/25-53-45-36/37-26
WGK Germany 
3
RTECS 
XF8060000
3-8-10
TSCA 
Yes
HS Code 
29341000
Hazardous Substances Data
298-93-1(Hazardous Substances Data)

MSDS

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Thiazolyl Blue Usage And Synthesis

Chemical Properties

Thiazolyl Blue Tetrazolium Blue (MTT) is a water soluble tetrazolium salt yielding a yellowish solution when prepared in media or salt solutions lacking phenol red. Dissolved MTT is converted to an insoluble purple formazan by cleavage of the tetrazolium ring by dehydrogenase enzymes. This water insoluble formazan can be solubilized using isopropanol or other solvents and the dissolved material is measured spectrophotometrically yielding absorbance as a function of concentration of converted dye.

Uses

Thiazolyl Blue Tetrazolium Blue (MTT) may be used in measurement of cell proliferation. MTT produces a yellowish solution that is converted to dark blue, water-insoluble MTT formazan by mitochondrial dehydrogenases of living cells. The blue crystals are solubilized with acidified isopropanol and the intensity is measured colorimetrically at 570 nm. MTT has been used as a histochemical/cytochemical reagent and for the detection of NAD. ADP-linked enzyme systems in tissue cannot be detected with MTT, due to binding of the cation by the cyanide trap used. MTT is rapidly reduced to the formazan, which chelates with nickel, copper, and cobalt; the cobalt chelate has been used in oxidative systems.

Definition

ChEBI: Thiazolyl Blue is the bromide salt of 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium. It has a role as a dye and a colorimetric reagent. It contains a 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium.

General Description

Thiazolyl Blue (MTT, Tetrazolium bromide, Methylthiazolyldiphenyl-tetrazolium bromide, Methylthialazole Tetrazolium) is a cell-permeable and positively charged colorimetric agent that is widely used to detect reductive metabolism in cells and to measure cell proliferation, cytotoxicity, and apoptosis. It is used as a direct indicator of cytotoxicity (such as for screening cancer drugs) and apoptosis. Thiazolyl Blue (MTT) is reduced from yellow color to purple formazan in living cells. As an electron acceptor, it is utilized for studying nicotinamide adenine dinucleotide phosphate (NADP)-dependent dehydrogenases.

Biochem/physiol Actions

Cell permeable: yes

storage

+4°C

Purification Methods

It is recrystallised by dissolving in MeOH containing a few drops of HBr and then adding dry Et2O to complete the crystallisation, wash the needles with Et2O and dry them in a vacuum desiccator over KOH. [Beyer & Pyl Chem Ber 87 1505 1954, Beilstein 27 III/IV 6045.]

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