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7385-67-3 molecular structure
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8-(diethylamino)-12H-10-oxa-5-azatetraphen-12-one

ChemBase ID: 103420
Molecular Formular: C20H18N2O2
Molecular Mass: 318.36912
Monoisotopic Mass: 318.13682783
SMILES and InChIs

SMILES:
CCN(CC)c1ccc2nc3c(oc2c1)cc(=O)c1c3cccc1
Canonical SMILES:
CCN(c1ccc2c(c1)oc1c(n2)c2ccccc2c(=O)c1)CC
InChI:
InChI=1S/C20H18N2O2/c1-3-22(4-2)13-9-10-16-18(11-13)24-19-12-17(23)14-7-5-6-8-15(14)20(19)21-16/h5-12H,3-4H2,1-2H3
InChIKey:
VOFUROIFQGPCGE-UHFFFAOYSA-N

Cite this record

CBID:103420 http://www.chembase.cn/molecule-103420.html

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NAMES AND DATABASE IDS

NAMES AND DATABASE IDS

Names Database IDs
IUPAC name
8-(diethylamino)-12H-10-oxa-5-azatetraphen-12-one
IUPAC Traditional name
nile red
Synonyms
Nile Red
Nile Blue A Oxazone
9-diethylamino-5H-benzo-alpha-phenoxazine-5-one
NILE RED
ChemDose™, N,N′-Dicyclohexylcarbodiimide impregnated tablets
DCC impregnated tablets
N,N′-Dicyclohexylcarbodiimide, ChemDose™ tablets
ChemDose™,N,N′-二环己基碳二亚胺浸渍片剂
DCC 浸渍片剂
N,N′-二环己基碳二亚胺,ChemDose™ 片剂
CAS Number
7385-67-3
538-75-0
EC Number
230-966-0
MDL Number
MFCD00011639
Beilstein Number
279110
PubChem SID
24886408
24851476
24897612
24885835
162091307
PubChem CID
65182

CALCULATED PROPERTIES

CALCULATED PROPERTIES

JChem
Acid pKa 14.3109455  H Acceptors
H Donor LogD (pH = 5.5) 3.8231463 
LogD (pH = 7.4) 3.8338141  Log P 3.833952 
Molar Refractivity 99.0239 cm3 Polarizability 35.514828 Å3
Polar Surface Area 41.9 Å2 Rotatable Bonds
Lipinski's Rule of Five true 

PROPERTIES

PROPERTIES

Physical Property Safety Information Product Information Bioassay(PubChem)
Melting Point
203-205 °C(lit.) expand Show data source
203-205°C expand Show data source
205-215 °C expand Show data source
Absorption Wavelength
λmax 553 nm expand Show data source
Fluorescence
λex 530 nm; λem 635 nm in methanol expand Show data source
Storage Condition
Room Temperature (15-30°C) expand Show data source
European Hazard Symbols
Toxic Toxic (T) expand Show data source
UN Number
2811 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
Hazard Class
6.1 expand Show data source
Packing Group
2 expand Show data source
Risk Statements
22-24-40-41-43 expand Show data source
Safety Statements
26-36/37/39-45 expand Show data source
GHS Pictograms
GHS05 expand Show data source
GHS07 expand Show data source
GHS08 expand Show data source
GHS Signal Word
Danger expand Show data source
GHS Hazard statements
H312-H317-H318-H351 expand Show data source
GHS Precautionary statements
P280-P305 + P351 + P338 expand Show data source
Personal Protective Equipment
Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges expand Show data source
Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter expand Show data source
RID/ADR
UN 2811 6.1/PG 2 expand Show data source
Purity
≥98.0% (HPLC) expand Show data source
Grade
for microscopy expand Show data source
Certificate of Analysis
Download expand Show data source
Suitability
suitable for fluorescence expand Show data source
Matrix
Magnesium aluminometasilicate base material expand Show data source
Product Line
BioReagent expand Show data source
Linear Formula
C6H11N=C=NC6H11 expand Show data source
Empirical Formula (Hill Notation)
C20H18N2O2 expand Show data source

DETAILS

DETAILS

MP Biomedicals MP Biomedicals Sigma Aldrich Sigma Aldrich
MP Biomedicals - 02151744 external link
Fluorescent stain for intracellular lipid droplets.
Sigma Aldrich - N3013 external link
Application
Fluorescent probe of intracellular lipids and hydrophobic domains of proteins.
包装
1 g in glass bottle
100 mg in glass bottle
Sigma Aldrich - 19123 external link
Frequently Asked Questions
Live Chat and Frequently Asked Questions are available for this Product.
Sigma Aldrich - 685178 external link
Frequently Asked Questions
Live Chat and Frequently Asked Questions are available for this Product.
Legal Information
ChemDose is a trademark of Reaxa Ltd.

REFERENCES

REFERENCES

From Suppliers Google Scholar IconGoogle Scholar PubMed iconPubMed Google Books IconGoogle Books
  • • Hist. Cyto., 33: 833 (1985).
  • • J. Cell. Biol., 100: 965 (1985).
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PATENTS

PATENTS

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INTERNET

INTERNET

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