Chemodex

TMA-DPH

CHF 226.00
In stock
CDX-T0043-M02525 mgCHF 226.00
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Product Details
Synonyms N,N,N-Trimethyl-4-(6-phenyl-1,3,5-hexatrien-1-yl)phenylammonium p-toluenesulfonate; 1,6-Diphenyl-1,3,5-hexatriene-4'-trimethylammonium tosylate; 1-(4-Trimethylammoniophenyl)-6-phenyl-1,3,5-hexatriene p-toluenesulfonate
Product Type Chemical
Properties
Formula C21H24N . C7H7O3S
MW 461.62
CAS 115534-33-3
Source/Host Chemicals Synthetic
Purity Chemicals ≥96% (TLC)
Appearance Yellow, dark yellow to beige powder.
Solubility Soluble in DMSO (10mg/ml) or methanol (1mg/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 ZKARERKEBVSZCX-VMDDUYISSA-M
Smiles C[N+](C)(C)C(C=C1)=CC=C1/C=C/C=C/C=C/C2=CC=CC=C2.CC3=CC=C(S([O-])(=O)=O)C=C3
Shipping and Handling
Shipping AMBIENT
Short Term Storage +20°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
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Product Specification Sheet
Datasheet Download PDF
Description

TMA-DPH is a fluorescent probe for membrane fluidity measurements in artificial and living membrane systems. Acts as an anchor at the lipid/water interface. Specifically and rapidly incorporating into the plasma membrane and between the membranes and the buffer. It is especially useful in the study of monolayer dynamics of lipoproteins and similar analogous systems, exocytosis kinetics and similar systems. TMA-DPH is cylinder-shaped and has fluorescence emission transition dipoles that are basically aligned parallel to its long molecular axis. As such, it is very sensitive to reorientation resulting from interactions with surrounding lipids. TMA-DPH is widely used in fluorescence polarization studies of rotational motion. Spectral Data: λex 355 nm; λem ~430 nm in methanol or DMSO.

Product References

(1) D. Illinger, et al.; Cell Biophys. 14, 17 (1989) | (2) C. Maire, et al.; Biorheology 29, 507 (1992) | (3) G. Ferretti, et al.; Biochim. Biophys. Acta 1147, 245 (1993) | (4) D. Illinger, et al.; J. Cell Biol. 125, 783 (1994) | (5) D. Illinger, et al.; Biochim. Biophys. Acta 1239, 58 (1995) | (6) J. Matko & P. Nagy; J. Photochem. Photobiol. B 40, 120 (1997) | (7) C. Saldana, et al.; J. Membr. Biol. 190, 75 (2002) | (8) B. Chazotte; Cold Spring Harb. Protoc. (2011) | (9) A.M.T.M. do Canto, et al.; Biochim. Biophys. Acta 1858, 2647 (2016)

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