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Merck

257621

Sigma-Aldrich

2,2-Di(4-tert-octylphenyl)-1-picrylhydrazyl, free radical

Synonim(y):

2,2-Bis[4-(1,1,3,3-tetramethylbutyl)phenyl]-1-(2,4,6-trinitrophenyl)hydrazinyl, 2,2-Di(4-tert-octylphenyl)-1-picrylhydrazyl, DPPH

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About This Item

Wzór empiryczny (zapis Hilla):
C34H44N5O6
Numer CAS:
Masa cząsteczkowa:
618.74
Numer MDL:
Kod UNSPSC:
12352005
Identyfikator substancji w PubChem:
NACRES:
NA.22

Postać

solid

Poziom jakości

mp

171 °C (dec.) (lit.)

λmaks.

531 nm

temp. przechowywania

2-8°C

ciąg SMILES

CC(C)(C)CC(C)(C)c1ccc(cc1)N([N]c2c(cc(cc2[N+]([O-])=O)[N+]([O-])=O)[N+]([O-])=O)c3ccc(cc3)C(C)(C)CC(C)(C)C

InChI

1S/C34H44N5O6/c1-31(2,3)21-33(7,8)23-11-15-25(16-12-23)36(26-17-13-24(14-18-26)34(9,10)22-32(4,5)6)35-30-28(38(42)43)19-27(37(40)41)20-29(30)39(44)45/h11-20H,21-22H2,1-10H3

Klucz InChI

CLOCMRDQPYXVKP-UHFFFAOYSA-N

Opis ogólny

2,2-Di(4-tert-octylphenyl)-1-picrylhydrazyl (DPPH) is classified as a “stable” free radical since it has a long shelf life and can be synthesized and stored under normal laboratory conditions.

Zastosowanie

2,2-Di(4-tert-octylphenyl)-1-picrylhydrazyl can be used as a calibration standard in electron paramagnetic spectroscopy (EPR) and as a radical scavenger in polymers. It is also used as an efficient reagent in the “DPPH calorimetric assay” to study radical scavenging activities of diverse chemical compounds, mostly of phenolic nature. When DDPF reacts with antioxidant molecules, its color changes from deep purple to pale yellow, which allows the spectrophotometric determination of the antioxidant activity.
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Kod klasy składowania

11 - Combustible Solids

Klasa zagrożenia wodnego (WGK)

WGK 3

Temperatura zapłonu (°F)

Not applicable

Temperatura zapłonu (°C)

Not applicable


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Dokumenty związane z niedawno zakupionymi produktami zostały zamieszczone w Bibliotece dokumentów.

Odwiedź Bibliotekę dokumentów

Ramona Figat et al.
Molecules (Basel, Switzerland), 25(5) (2020-03-04)
Traditional medicinal plants are an important source of active compounds with potential antimutagenic activity. Polyscias filicifolia Bailey (Araliaceae) is a South Asian traditional herb used as an adaptogenic and cardiac drug. Extracts of P. filicifolia contain a wide range of
Joaquín Navarro Del Hierro et al.
Food chemistry, 309, 125742-125742 (2019-11-11)
Extracts from the edible insects Acheta domesticus and Tenebrio molitor were obtained by ultrasound-assisted extraction (UAE) and pressurized-liquid extraction (PLE) using ethanol (E) or ethanol:water (E:W). Characterization by GC-MS was performed and total phenolic compounds (TPC), antioxidant activity (DPPH) and
Jian-Xin Diao et al.
Chinese journal of integrative medicine, 26(10), 736-744 (2019-11-27)
To investigate the phenolic composition, antioxidant properties, and hepatoprotective mechanisms of polyphenols from green tea extract (GTP) in carbon tetrachloride (CCl4)-induced acute liver injury mouse model. High-performance liquid chromatography was used to analyze the chemical composition of the extract. Antioxidant
Konrad A Szychowski et al.
Pesticide biochemistry and physiology, 168, 104638-104638 (2020-07-28)
Triclosan (TCS) is commonly used worldwide in a range of personal care and sanitizing products. A number of studies have revealed the presence of TCS in human tissues. It has recently been shown that TCS can interact with AhR in
Azis Boing Sitanggang et al.
Journal of food science and technology, 57(12), 4660-4670 (2020-10-23)
The influences of coagulation conditions on the characteristics of tofu have been investigated by many studies, with limited perspectives on the utilization of organic acid coagulants. Hence, this research aimed to study the psychochemical and functional properties of tofu coagulated

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