Thiazolyl Blue

Thiazolyl Blue Basic information
Product Name:Thiazolyl Blue
Synonyms: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;2-(4,5-dimethylthiazol-2-yl)-3,5-diphenyl-2htetrazolium 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
Thiazolyl Blue Structure
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
Sensitive Light Sensitive
λmax378 nm, 242 nm
BRN 3825277
Stability:Hygroscopic
Biological ApplicationsCell viability assay; microbial growth assays; DNA quantification assays; tissue viability assays; detecting enzymes; measuring membrane potential; treating Alzheimer’s disease,asthma,cancer
InChIKeyAZKSAVLVSZKNRD-UHFFFAOYSA-M
CAS DataBase Reference298-93-1(CAS DataBase Reference)
EPA Substance Registry System2H-Tetrazolium, 2-(4,5-dimethyl-2-thiazolyl)-3,5-diphenyl-, bromide (298-93-1)
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 Data298-93-1(Hazardous Substances Data)
MSDS Information
Thiazolyl Blue Usage And Synthesis
Chemical PropertiesThiazolyl 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.
UsesThiazolyl 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.
DefinitionChEBI: 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 DescriptionThiazolyl 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 ActionsCell permeable: yes
storage+4°C
Purification MethodsIt 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.]
Thiazolyl Blue Preparation Products And Raw materials
Fmoc-Gln(Mtt)- (200-400 mesh) H-Lys(Mtt)-2-chlorotrityl- (200-400 mesh) (4S)-3-(FMOC-ASN (MTT))-2,2-DIMETHYL-OXAZOLIDINE-4-CARBOXYLIC ACID,FMOC-ASN(MTT)-SER(PSI(ME,ME)PRO)-OH Fmoc-D-Asn(Mtt)-SASRIN- (200-400 mesh) Fmoc-Lys(Mtt)-SASRIN- (200-400 mesh) H-L-His(Mtt)-2-chlorotrityl resin (100-200 mesh, > 0.5 mmol Fmoc-D-His(1-Mtt)-OH,Fmoc-D-His(tau-Mtt)-OH Mtt-Cl Resin Fmoc-D-Gln(Mtt)-SASRIN- (200-400 mesh) FMOC-ASN(MTT)-ALKO RESIN,FMOC-ASN(MTT)-WANG RESIN Clidinium bromide Fmoc-D-Gln(Mtt)- (200-400 mesh) THIAZOLYL BLUE FORMAZAN,thiazolyl blue formazane Bromide Fmoc-D-Asn(Mtt)- (200-400 mesh) Fmoc-Lys(Mtt)- (200-400 mesh) FMOC-ASN(MTT)-P-ALKOXYBENZYL ALCOHOL RESIN,FMOC-ASN(MTT)-SASRIN(TM)-RESIN 2-(2-Aminothiazol-4-yl)glyoxylic acid

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