Specifications
- Purity
- ≥95% (Dye content)
- Appearance
- Beige to yellow-brown powder
Properties
- Solvents
- ethanol (30 mg/ml).
- Melting Point
- 225 °C (dec.)(lit.)
- UV / Vis
- 423 nm
Available from stock
Bromocresol Green
- SKU
- B0264
Category: Non Fluorescent Detection & Chromogene Detection
- Synonyms
- "3',3"",5',5""-Tetrabromo-m-cresolsulfonephthalein , NSC 7817 , BCG"
- 76-60-8
- CAS-Number
- C21H14Br4O5S
- Molecular Formula
- 698.01
- Molecular Weight
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
- Shipping
- AMBIENT
- Short Term Storage
- RT
- Long Term Storage
- RT
- Handling Advice
- Protect from light and moisture.
- Use / Stability
- Stable for at least 2 years after receipt when stored at RT.
- Transportation
- Not dangerous goods
- 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.
- 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
- InChi Key
- FRPHFZCDPYBUAU-UHFFFAOYSA-N
- 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)
- InChi
- InChI=1S/C21H14Br4O5S/c1-9-12(7-14(22)19(26)17(9)24)21(13-8-15(23)20(27)18(25)10(13)2)11-5-3-4-6-16(11)31(28,29)30-21/h3-8,26-27H,1-2H3
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.
Additional information
| Synonyms | "3',3"",5',5""-Tetrabromo-m-cresolsulfonephthalein, NSC 7817, BCG" |
|---|---|
| Purity | ≥95% (Dye content) |
| Appearance | Beige to yellow-brown powder |
| CAS-Number | 76-60-8 |
| Molecular Formula | C21H14Br4O5S |
| Molecular Weight | 698.01 |
| Solvents | ethanol (30 mg/ml). |
| Melting Point | 225 °C (dec.)(lit.) |
| UV / Vis | 423 nm |
| 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 |
| InChi Key | FRPHFZCDPYBUAU-UHFFFAOYSA-N |
| Shipping | AMBIENT |
| Short Term Storage | RT |
| Long Term Storage | RT |
| Handling Advice | Protect from light and moisture. |
| Use / Stability | Stable for at least 2 years after receipt when stored at RT. |
| Transportation | Not dangerous goods |
| 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) |
| InChi | InChI=1S/C21H14Br4O5S/c1-9-12(7-14(22)19(26)17(9)24)21(13-8-15(23)20(27)18(25)10(13)2)11-5-3-4-6-16(11)31(28,29)30-21/h3-8,26-27H,1-2H3 |
| Quantity | 25 g, Bulk |
