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1320-06-5 molecular structure
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1-(2-{4-[2-(2,5-dimethylphenyl)diazen-1-yl]-2,5-dimethylphenyl}diazen-1-yl)naphthalen-2-ol

ChemBase ID: 104453
Molecular Formular: C26H24N4O
Molecular Mass: 408.49496
Monoisotopic Mass: 408.19501141
SMILES and InChIs

SMILES:
Cc1cc(/N=N/c2cc(C)c(cc2C)/N=N/c2c3ccccc3ccc2O)c(C)cc1
Canonical SMILES:
Cc1ccc(c(c1)/N=N/c1cc(C)c(cc1C)/N=N/c1c(O)ccc2c1cccc2)C
InChI:
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
InChIKey:
NPGIHFRTRXVWOY-UHFFFAOYSA-N

Cite this record

CBID:104453 http://www.chembase.cn/molecule-104453.html

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NAMES AND DATABASE IDS

NAMES AND DATABASE IDS

Names Database IDs
IUPAC name
1-(2-{4-[2-(2,5-dimethylphenyl)diazen-1-yl]-2,5-dimethylphenyl}diazen-1-yl)naphthalen-2-ol
1-[(E)-2-{4-[(E)-2-(2,5-dimethylphenyl)diazen-1-yl]-2,5-dimethylphenyl}diazen-1-yl]naphthalen-2-ol
IUPAC Traditional name
1-(2-{4-[2-(2,5-dimethylphenyl)diazen-1-yl]-2,5-dimethylphenyl}diazen-1-yl)naphthalen-2-ol
oil red O
Synonyms
Solvent Red 27
OIL RED O
1-[2,5-Dimethyl-4-(2,5-dimethylphenylazo)phenylazo]-2-naphthol
1-([4-(Xylylazo)xylyl]azo)-2-naphthol
Oil Red O
C.I. 26125
1-((4-((2,5-Dimethylphenyl)diazenyl)-2,5-dimethylphenyl)diazenyl)naphthalen-2-ol
1-([4-(二甲苯偶氮)二甲苯]偶氮)-2-萘酚
油红
溶剂红 27
油红 O
CAS Number
1320-06-5
EC Number
215-295-3
MDL Number
MFCD00003898
Beilstein Number
3491382
PubChem SID
162091563
24898072
24897931
PubChem CID
5841742
6046885
Chemspider ID
14217961
MeSH Name
oil+red+O
Wikipedia Title
Oil_Red_O
Color Index Number
26125

CALCULATED PROPERTIES

CALCULATED PROPERTIES

JChem
Acid pKa 11.335133  H Acceptors
H Donor LogD (pH = 5.5) 9.524625 
LogD (pH = 7.4) 9.52458  Log P 9.524631 
Molar Refractivity 133.2919 cm3 Polarizability 48.02838 Å3
Polar Surface Area 69.67 Å2 Rotatable Bonds
Lipinski's Rule of Five false 

PROPERTIES

PROPERTIES

Physical Property Safety Information Product Information Bioassay(PubChem)
Apperance
powder expand Show data source
Melting Point
120 °C (dec.)(lit.) expand Show data source
120°C (dec) expand Show data source
ca 166°C dec. expand Show data source
Absorption Wavelength
λmax 359 nm expand Show data source
λmax 518 nm (2nd) expand Show data source
Storage Condition
Room Temperature (15-30°C) expand Show data source
MSDS Link
Download expand Show data source
Download expand Show data source
Download expand Show data source
Download expand Show data source
German water hazard class
3 expand Show data source
TSCA Listed
expand Show data source
Personal Protective Equipment
Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter expand Show data source
Purity
95+% expand Show data source
Grade
certified by the Biological Stain Commission expand Show data source
for microscopy expand Show data source
Compostion
Dye content, ≥75% expand Show data source
Certificate of Analysis
Download expand Show data source
Suitability
suitable for electrophoresis expand Show data source
Product Line
BioReagent expand Show data source
Empirical Formula (Hill Notation)
C26H24N4O expand Show data source

DETAILS

DETAILS

MP Biomedicals MP Biomedicals Wikipedia Wikipedia Sigma Aldrich Sigma Aldrich
MP Biomedicals - 02155984 external link
C.l. 26125 (Solvent Red 27; 1-[(4-[Xylylazo]xylyl)azo]-2-naphthol) Lipid stain on cellulose acetate. Green powder.
Sigma Aldrich - O9755 external link
Application
Oil Red O stain is suitable as a lipid/lipoprotein stain on cellulose acetate. A 0.2% stock solution is prepared in methanol. The stock solution (35 ml) is diluted with 10 mL of 1 M NaOH immediately before staining. The dye begins precipitating during staining. After staining (1 hr), the membrane is destained in methanol:glycerol (1:3). Often cited for use with agarose
Sigma Aldrich - 75087 external link
Other Notes
Lipoprotein stain on celluloseacetate plates1
Sigma Aldrich - O0625 external link
Frequently Asked Questions
Live Chat and Frequently Asked Questions are available for this Product.
Packaging
25, 100 g in glass bottle
Suitability
Certified for use as a fat stain in Churukian′s modification of the method of Lillie and Asburn.

REFERENCES

REFERENCES

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PATENTS

PATENTS

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INTERNET

INTERNET

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