Chemodex

Bromocresol Green

CHF 150.00
In stock
CDX-B0264-G02525 gCHF 150.00
More Information
Product Details
Synonyms 3',3",5',5"-Tetrabromo-m-cresolsulfonephthalein; NSC 7817; BCG
Product Type Chemical
Properties
Formula

C21H14Br4O5S

MW 698.01
CAS 76-60-8
RTECS SJ7456000
Purity Chemicals ≥95% (Dye content)
Appearance Beige to yellow-brown powder.
Solubility Soluble in ethanol (30mg/ml).
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 FRPHFZCDPYBUAU-UHFFFAOYSA-N
Smiles O=S1(C2=CC=CC=C2C(C3=CC(Br)=C(O)C(Br)=C3C)(C4=C(C)C(Br)=C(O)C(Br)=C4)O1)=O
Shipping and Handling
Shipping AMBIENT
Short Term Storage +20°C
Long Term Storage +20°C
Handling Advice Protect from light and moisture.
Use/Stability Stable for at least 2 years after receipt when stored at RT.
Documents
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Product Specification Sheet
Datasheet Download PDF
Description

Bromocresol green (BCG) is a pH sensitive triphenylmethane dye useful in a variety of colorimetric detection technologies. BCG is used as a tracking dye for DNA agarose gel electrophoresis, in protein determinations and in charge-transfer complexation processes. In TLC BCG is used for visualization of the compounds with functional groups whose pKa is below 5.0. One major use is to measure serum albumin concentration within mammalian blood samples in possible cases of kidney failure and liver disease. In aqueous solution, bromocresol green will ionize to give the monoanionic form (yellow), that further deprotonates at higher pH to give the dianionic form (blue). Visual transition interval: pH 3.8 (yellow) - 5.4 (blue). UV-Visible (λmax): 423 nm, 444 nm, 617 nm. Bromocresol green is also an inhibitor of prostaglandin uptake that blocks the immediate rise in intracellular immunoreactive PGE2 following treatment with 16,16-dimethyl-PGE2. Bromocresol green prevents the stimulatory effect of 16,16-dimethyl-PGE on cell proliferation, adhesion, migration and invasion and on HIF-1α expression and activity. Additional applications include use in sol-gel matrices and the detection of ammonia.

Product References

(1) P.G. Hill; Ann. Clin. Biochem. 22, 565 (1985) | (2) F.R. Zaggout; J. Disp. Sci. Technol. 26, 757 (2005) | (3) R.W. Sabnis; Handbook of Acid-Base Indicators (2008) | (4) A. Madrigal-Martinez, et al.; Int. J. Biochem. Cell Biol. 59, 52 (2015)

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