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21742

Sigma-Aldrich

4-Nitrophenyl octanoate

≥90.0% (GC), liquid

Synonym(s):

4-Nitrophenyl caprylate, Caprylic acid 4-nitrophenyl ester, Octanoic acid 4-nitrophenyl ester

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About This Item

Empirical Formula (Hill Notation):
C14H19NO4
CAS Number:
Molecular Weight:
265.30
Beilstein/REAXYS Number:
8989916
MDL number:
UNSPSC Code:
12352204
PubChem Substance ID:
NACRES:
NA.83

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Product Name

4-Nitrophenyl octanoate, ≥90.0% (GC)

Quality Level

assay

≥90.0% (GC)

form

liquid

refractive index

n20/D 1.510

density

1.095 g/mL at 20 °C (lit.)

storage temp.

2-8°C

SMILES string

CCCCCCCC(=O)Oc1ccc(cc1)[N+]([O-])=O

InChI

1S/C14H19NO4/c1-2-3-4-5-6-7-14(16)19-13-10-8-12(9-11-13)15(17)18/h8-11H,2-7H2,1H3

InChI key

GGIDEJQGAZSTES-UHFFFAOYSA-N

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1 of 4

This Item
N4377N8130N3627
assay

≥90.0% (GC)

assay

≥98% (TLC)

assay

≥98% (TLC)

assay

≥90% (TLC)

Quality Level

100

Quality Level

200

Quality Level

200

Quality Level

200

form

liquid

form

liquid

form

powder or crystals

form

powder

storage temp.

2-8°C

storage temp.

−20°C

storage temp.

−20°C

storage temp.

−20°C

refractive index

n20/D 1.510

refractive index

-

refractive index

-

refractive index

-

density

1.095 g/mL at 20 °C (lit.)

density

-

density

-

density

-

pictograms

Exclamation mark

signalword

Warning

hcodes

pcodes

Hazard Classifications

Skin Sens. 1

Storage Class

10 - Combustible liquids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Faceshields, Gloves


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Jared M Campbell et al.
BMC cancer, 19(1), 1242-1242 (2019-12-23)
Cell cycle analysis is important for cancer research. However, available methodologies have drawbacks including limited categorisation and reliance on fixation, staining or transformation. Multispectral analysis of endogenous cell autofluorescence has been shown to be sensitive to changes in cell status
A Combined Conductivity and XAS Study of Plastically Crystalline Electrolytes.
Chadwick AV, et al.
Journal of Physics. Conference Series, 249(1) (2010)
Possible role of hydroxyl radicals in the metabolism of succinonitrile.
E P Hayes et al.
Biochemical pharmacology, 34(22), 4081-4084 (1985-11-15)
B W Mangum
Clinical chemistry, 29(7), 1380-1384 (1983-07-01)
In an investigation of the melting and freezing behavior of succinonitrile, the triple-point temperature was determined to be 58.0805 degrees C, with an estimated uncertainty of +/- 0.0015 degrees C relative to the International Practical Temperature Scale of 1968 (IPTS-68).
Tijs M Lammens et al.
ChemSusChem, 4(6), 785-791 (2011-05-11)
Succinonitrile is the precursor of 1,4-diaminobutane, which is used for the industrial production of polyamides. This paper describes the synthesis of biobased succinonitrile from glutamic acid and glutamine, amino acids that are abundantly present in many plant proteins. Synthesis of

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