Bromocresol purple

Bromocresol purple
Skeletal formula of bromocresol purple in cyclic form
Ball-and-stick model of the bromocresol purple molecule in cyclic form
Names
Preferred IUPAC name
3,3-Bis(3-bromo-4-hydroxy-5-methylphenyl)-2,1λ6-benzoxathiole-1,1(3H)-dione
Other names
5′,5′′-Dibromo-o-cresolsulfonephthalein
Bromcresol purple
Identifiers
3D model (JSmol)
ChEBI
ChemSpider
ECHA InfoCard 100.003.716 Edit this at Wikidata
EC Number
  • 204-087-8
UNII
  • InChI=1S/C21H16Br2O5S/c1-11-7-13(9-16(22)19(11)24)21(14-8-12(2)20(25)17(23)10-14)15-5-3-4-6-18(15)29(26,27)28-21/h3-10,24-25H,1-2H3 checkY
    Key: ABIUHPWEYMSGSR-UHFFFAOYSA-N checkY
  • InChI=1/C21H16Br2O5S/c1-11-7-13(9-16(22)19(11)24)21(14-8-12(2)20(25)17(23)10-14)15-5-3-4-6-18(15)29(26,27)28-21/h3-10,24-25H,1-2H3
    Key: ABIUHPWEYMSGSR-UHFFFAOYAH
  • InChI=1/C21H17BrO5S/c1-12-9-14(7-8-18(12)23)21(15-10-13(2)20(24)17(22)11-15)16-5-3-4-6-19(16)28(25,26)27-21/h3-11,23-24H,1-2H3
  • Brc1c(O)c(cc(c1)C3(OS(=O)(=O)c2ccccc23)c4cc(c(O)c(Br)c4)C)C
Properties
C21H16Br2O5S
Molar mass 540.22 g·mol−1
Appearance Purple powder
Melting point 241 to 242 °C (466 to 468 °F; 514 to 515 K) (decomposition)
< 0.1 %
Hazards
GHS labelling:
GHS07: Exclamation mark
Warning
H315, H319, H335
P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, P501
NFPA 704 (fire diamond)
NFPA 704 four-colored diamondHealth 1: Exposure would cause irritation but only minor residual injury. E.g. turpentineFlammability 0: Will not burn. E.g. waterInstability 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g. liquid nitrogenSpecial hazards (white): no code
1
0
0
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
☒N verify (what is checkY☒N ?)

Bromocresol purple (BCP) or 5′,5″-dibromo-o-cresolsulfophthalein, is a dye of the triphenylmethane family (triarylmethane dyes) and a pH indicator. It is colored yellow below pH 5.2, and violet above pH 6.8. In its cyclic sulfonate ester form, it has a pKa value of 6.3, and is usually prepared as a 0.04% aqueous solution.[1]

Uses

A sample of bromocresol purple in its violet form
Bromocresol purple (pH indicator)
below pH 5.2 above pH 6.8
5.2 ⇌ 6.8

Bromocresol purple is used in medical laboratories to measure albumin. Use of BCP in this application may provide some advantage over older methods using bromocresol green.[2][3] In microbiology, it is used for staining dead cells based on their acidity, and for the isolation and assaying of lactic acid bacteria.[4][5]

In photographic processing, it can be used as an additive to acid stop baths to indicate that the bath has reached neutral pH and needs to be replaced.[6]

Bromocresol purple milk solids glucose agar is used as a medium used to distinguish dermatophytes from bacteria and other organisms in cases of ringworm fungus (T. verrucosum) infestation in cattle and other animals.[7][8]

pH Indicator

Similar to bromocresol green, the structure of bromocresol purple changes with pH. Changing the level of acidity causes a shift in the equilibrium between two different structures that have different colors. In near-neutral or alkaline solution, the chemical has a sulfonate structure that gives the solution a purple color. As the pH decreases, it converts to a sultone (cyclic sulfonic ester) that colors the solution yellow. In some microbiology tests, this change is used as an indicator of bacterial growth.[9][10]

See also

References

  1. ^ "Bromocresol Purple". NCBI PubChem. National Center for Biotechnology Information.
  2. ^ Bachmann, Lorin M.; Yu, Min; Boyd, James C.; Bruns, David E.; Miller, W. Greg (2017-03-01). "State of Harmonization of 24 Serum Albumin Measurement Procedures and Implications for Medical Decisions". Clinical Chemistry. 63 (3): 770–779. doi:10.1373/clinchem.2016.262899. ISSN 0009-9147. PMID 28073902.
  3. ^ Ito, Shigenori; Yamamoto, Daisuke (2010-02-02). "Mechanism for the color change in bromocresol purple bound to human serum albumin". Clinica Chimica Acta. 411 (3): 294–295. doi:10.1016/j.cca.2009.11.019. PMID 19932090.
  4. ^ Kurzweilová, H.; Sigler, K. (November 1993). "Fluorescent staining with bromocresol purple: a rapid method for determining yeast cell dead count developed as an assay of killer toxin activity". Yeast. 9 (11): 1207–1211. doi:10.1002/yea.320091107. PMID 7509098. S2CID 44782970.
  5. ^ Lee, H.M.; Lee, Y. (June 2008). "A differential medium for lactic acid-producing bacteria in a mixed culture". Letters in Applied Microbiology. 46 (6): 676–681. doi:10.1111/j.1472-765X.2008.02371.x. PMID 18444977. Open access icon
  6. ^ Anchell, Steve (2016). The Darkroom Cookbook (4 ed.). Routledge. ISBN 9781317337607 – via Google Books.
  7. ^ Kane, J.; Summerbell, R.; Sigler, L.; Krajden, S.; Land, G. (1997). Laboratory Handbook of Dermatophytes: A Clinical Guide and Laboratory Handbook of Dermatophytes and Other Filamentous Fungi from Skin, Hair, and Nails. Belmont, CA: Star Publishing Company. ISBN 9780898631579.
  8. ^ Beneke, E. S.; Rogers, A. L. (1996). Medical Mycology and Human Mycoses (illustrated ed.). Belmont, CA: Star Publishing Company. pp. 85–90. ISBN 9780898631753.
  9. ^ "Bromocresol Purple - an overview | ScienceDirect Topics".
  10. ^ "Archived copy". Archived from the original on 2022-02-16. Retrieved 2022-02-15.{{cite web}}: CS1 maint: archived copy as title (link)
Wikimedia Commons has media related to Bromocresol purple.