Key Documents

1,1-Diphenyl-2-picrylhydrazine

Name: 1,1-Diphenyl-2-picrylhydrazine
Brand: ALDRICH

97%

Synonym(s):

α,α-Diphenyl-β-picrylhydrazine, 1,1-Diphenyl-2-(2,4,6-trinitrophenyl)hydrazine, 2,2-Diphenyl-1-(2,4,6-trinitrophenyl)hydrazine, 2,2-Diphenyl-1-picrylhydrazine, Diphenylpicrylhydrazine

About This Item

Linear Formula:

2,4,6-(O₂N)₃C₆H₂NHN(C₆H₅)₂

CAS Number:

1707-75-1

Molecular Weight:

395.33

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

24856989

EC Number:

216-953-2

Beilstein/REAXYS Number:

770319

MDL number:

MFCD00007229

Assay:

97%

Form:

solid

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Properties

assay

97%

form

solid

mp

~174 °C (dec.) (lit.)

SMILES string

[O-][N+](=O)c1cc(c(NN(c2ccccc2)c3ccccc3)c(c1)[N+]([O-])=O)[N+]([O-])=O

InChI

1S/C18H13N5O6/c24-21(25)15-11-16(22(26)27)18(17(12-15)23(28)29)19-20(13-7-3-1-4-8-13)14-9-5-2-6-10-14/h1-12,19H

InChI key

WCBPJVKVIMMEQC-UHFFFAOYSA-N

Description

pictograms

GHS02,GHS08,GHS07

signalword

Danger

hcodes

H242,H302 + H312 + H332,H315,H317,H319,H334

pcodes

P210 - P235 - P280 - P302 + P352 + P312 - P370 + P378 - P403

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Resp. Sens. 1 - Self-react. C - Skin Irrit. 2 - Skin Sens. 1

Storage Class

4.1A - Other explosive hazardous materials

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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The reaction of oxyhemoglobin with 1,1-diphenyl-2-picrylhydrazine and 2,2-diphenyl-1-picrylhydrazyl.

P Smith et al.

Journal of inorganic biochemistry, 31(4), 247-253 (1987-12-01)

In an effort to elucidate the mechanism of the initiation reaction of the denaturation of oxyhemoglobin, I, to methemoglobin, II, by hydrazines, we have investigated by electron paramagnetic resonance, EPR, and visible spectrophotometry at 22 degrees C, pH 7.4, the

The surface reaction between manganese dioxide and 1, 1-diphenyl-2-picrylhydrazine. Two type EPR methods for the estimation of active surface areas of oxides.

Oei ATTT and Garnett JL.

J. Catal., 19(2), 176-194 (1970)

Inhibitory Potential of Constituents from Osmanthus fragrans and Structural Analogues Against Advanced Glycation End Products, α-Amylase, α-Glucosidase, and Oxidative Stress.

Ji-Yeon Yang et al.

Scientific reports, 7, 45746-45746 (2017-04-01)

Inhibition of α-amylase and α-glucosidase, advanced glycation end products (AGEs) formation, and oxidative stress by isolated active constituents of Osmanthus fragrans flowers (9,12-octadecadienoic acid and 4-(2,6,6-trimethyl-1-cyclohexenyl)-3-buten-2-one) and their structural analogues were evaluated. 9,12-Octadecadienoic acid was 10.02 and 22.21 times more

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Global Trade Item Number

SKU	GTIN
281689-1G	04061826225660

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