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Oil Red O

From Wikipedia, the free encyclopedia
Oil Red O
Differentiatedadipocytes in a3T3-L1 cell line stained with Oil Red O
Names
IUPAC name
1-(2,5-dimethyl-4-(2,5-dimethylphenyl) phenyldiazenyl) azonapthalen-2-ol
Identifiers
3D model (JSmol)
ChEBI
ChemSpider
ECHA InfoCard100.013.906Edit this at Wikidata
MeSHoil+red+O
UNII
  • InChI=1S/C26H24N4O/c1-16-9-10-17(2)22(13-16)27-28-23-14-19(4)24(15-18(23)3)29-30-26-21-8-6-5-7-20(21)11-12-25(26)31/h5-15,31H,1-4H3/b28-27+,30-29+ checkY
    Key: NPGIHFRTRXVWOY-XOXGWFOHSA-N checkY
  • InChI=1/C26H24N4O/c1-16-9-10-17(2)22(13-16)27-28-23-14-19(4)24(15-18(23)3)29-30-26-21-8-6-5-7-20(21)11-12-25(26)31/h5-15,31H,1-4H3/b28-27+,30-29+
    Key: NPGIHFRTRXVWOY-XOXGWFOHBH
  • Cc4cc(/N=N/c1cc(C)c(cc1C)/N=N/c2c3ccccc3ccc2O)c(C)cc4
Properties
C26H24N4O
Molar mass408.49496
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa).
☒N verify (what is checkY☒N ?)
Chemical compound

Oil Red O (Solvent Red 27,Sudan Red 5B,C.I. 26125, C26H24N4O) is alysochrome (fat-soluble dye)diazo dye used forstaining of neutraltriglycerides andlipids on frozen sections and somelipoproteins on paraffin sections. It has the appearance of a red powder with anabsorbance maximum at 518 nanometers.[1]

Uses

[edit]

Oil Red O is one of the dyes used forSudan staining. Similar dyes includeSudan III,Sudan IV, andSudan Black B. The staining has to be performed on fresh samples, as alcohol fixation removes most lipids. Oil Red O largely replaced Sudan III and Sudan IV, as it provides much deeper red color and the stains are therefore much easier to see.

Oil Red O can be used to mark lipid-containing vacuoles, particularly in cases ofacute lymphoblastic leukemia orBurkitt's lymphoma. It can also be used to stain liver sections for histological analysis, quantify cell lipid content, and to stain the aorta to examine lesions from atherosclerosis.[2]

Inpyrotechnics, Oil Red O is used in some compositions of redcolored smokes.

Forensic

[edit]

When staining, Oil Red O can make fat more visible in various cuts in pathology.[3]

It is also used in a technique (the method is called as the dye: Oil Red O), discovered in 2004 byAlexandre Beaudoin, for staining latentfingerprints.[4] This technique allows the development of latent fingerprints on porous exhibits (such as paper, cardboard, etc.) that are dry or wet.

It mainly targets fat deposits on the surface of porous exhibits.[5] It is a non-destructive technique (which does not destroy the exhibit nor prevents the use of other techniques).

It is a safe alternative to the Physical Developer method,[6] and is also used in sequence with other methods of fingerprints development.[7]

References

[edit]
  1. ^Kraus, Nils A.; Ehebauer, Franziska; Zapp, Benedikt; et al. (2016)."Quantitative assessment of adipocyte differentiation in cell culture".Adipocyte.5 (4):351–358.doi:10.1080/21623945.2016.1240137.ISSN 2162-3945.PMC 5160397.PMID 27994948.
  2. ^"Oil Red O".MilliporeSigma. Retrieved15 February 2023.
  3. ^"Forensic Pathology".
  4. ^Triplett M,Fingerprint Dictionary, Two Rings Publishing, Bellevue, Washington.
  5. ^Beaudoin, A. New technique for revealing latent fingerprints on wet, porous surfaces: Oil Red O. Journal of Forensic Identification, 2004, 54 (4), 413-421.
  6. ^Rawji, A. ; Beaudoin, A. Oil Red O versus Physical Developer on wet papers: a comparative study. Journal of Forensic Identification, 2006, 56 (1), 33-54.
  7. ^Guigui, K.; Beaudoin, A. The use of Oil Red O in sequence with other methods of fingerprint development. Journal of Forensic Identification, 2007, 57 (4), 550-581.

External links

[edit]
Iron/hemosiderin
Lipids
Carbohydrates
Amyloid
Bacteria
Connective tissue
Other
Tissue stainability
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