Chemodex

Thiazolyl blue tetrazolium bromide [MTT]

CHF 61.00
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CDX-T0186-G0011 gCHF 61.00
CDX-T0186-G0055 gCHF 244.00
CDX-T0186-G01010 gCHF 434.00
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Product Details
Synonyms 3-(4,5-Dimethyl-2-thiazolyl)-2,5-diphenyl-2H-tetrazolium bromide; MTT; Methylthiazolyldiphenyl-tetrazolium bromide; NSC 60102
Product Type Chemical
Properties
Formula C18H16BrN5S
MW 414.32
CAS 298-93-1
RTECS XF8060000
Source/Host Chemicals Synthetic
Purity Chemicals ≥98% (HPLC)
Appearance Yellow powder.
Solubility Soluble in water (5mg/ml).
Identity Determined by 1H-NMR.
Declaration Manufactured by Chemodex.
Other Product Data

Click here for Original Manufacturer Product Datasheet
Our product description may differ slightly from the original manufacturers product datasheet.

InChi Key AZKSAVLVSZKNRD-UHFFFAOYSA-M
Smiles CC1=C(C)SC([N+]2=NC(C3=CC=CC=C3)=NN2C4=CC=CC=C4)=N1.[Br-]
Shipping and Handling
Shipping AMBIENT
Short Term Storage +4°C
Long Term Storage +4°C
Handling Advice Protect from light and moisture.
Use/Stability Stable for at least 2 years after receipt when stored at +4°C.
Documents
MSDS Download PDF
Product Specification Sheet
Datasheet Download PDF
Description

MTT is a common histochemical/cytochemical reagent and for the detection of NAD. MTT is used to detect reductive metabolism in cells. It is a cell-permeable yellow dye that is reduced by intracellular NAD(P)H-oxidoreductases in mitochondria of living cells to form the dark blue water-insoluble MTT-formazan. The intensity of the color can then be measured spectrophotometrically at 540 or 570nm, which allows quantitation of cell viability and cell proliferation. It is frequently used in colorimetric assays to measure cell proliferation/cell growth, cytotoxicity (such as for screening cancer drugs), and apoptosis.

Product References

(1) M.A. Abdallah, & J.-F. Biellmann; Eur. J. Biochem. 112, 331 (1980) | (2) Y. Liu, et al.; J. Neurochem. 69, 581 (1997) | (3) M.V. Berridge, et al.; Biotechnol. Ann. Rev. 11, 127 (2005) | (4) T. Hayon, et al.; Leuk. Lymphoma 44, 1957 (2003) (Review) | (5) K. Praebst, et al.; Methods Mol. Biol. 1601, 1 (2017) | (6) P. Kumar, et al.; Cold Spring Harb. Protoc. 2018, pdb.prot095505 (2018) | (7) E. Grela, et al.; Acta Histochem. 120, 303 (2018) (Review)

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