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Merck
CN

D204838

Sigma-Aldrich

2-Diphenylacetyl-1,3-indandione-1-hydrazone

98%

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About This Item

Empirical Formula (Hill Notation):
C23H18N2O2
CAS Number:
5102-79-4
Molecular Weight:
354.40
EC Number:
225-821-3
MDL number:
MFCD00003783
UNSPSC Code:
12171500
PubChem Substance ID:
24893608
NACRES:
NA.47

Key Documents

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Assay

98%

form

powder, crystals or chunks

mp

241-243 °C (lit.)

solubility

acetone: 2 mg/mL, clear, yellow to brown

application(s)

diagnostic assay manufacturing
hematology
histology

storage temp.

room temp

SMILES string

N\N=C1\C(C(=O)C(c2ccccc2)c3ccccc3)C(=O)c4ccccc14

InChI

1S/C23H18N2O2/c24-25-21-17-13-7-8-14-18(17)22(26)20(21)23(27)19(15-9-3-1-4-10-15)16-11-5-2-6-12-16/h1-14,19-20H,24H2/b25-21+

InChI key

QBGMRRUHCFHZLC-NJNXFGOHSA-N

Pictograms

Skull and crossbonesEnvironment
GHS06,GHS09

Signal Word

Danger

Hazard Statements

H301,H410

Hazard Classifications

Acute Tox. 3 Oral - Aquatic Acute 1 - Aquatic Chronic 1

Storage Class Code

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
BGBB4080V
00321PE
00213LV
03308PV

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Effects of ethanol and glutamate agonist infusion on the outflow of sulphoacetaldehyde: microdialysis studies.
S Capodarca et al.
Advances in experimental medicine and biology, 483, 297-304 (2002-01-15)
Limitations of 2-diphenylacetyl-1,3-indandione-1-hydrazone as a precolumn fluorescence derivatization reagent.
M A Heindorf et al.
Journal of chromatography, 464(1), 186-194 (1989-02-17)
[Quantitative determination of oxoline].
Z B Moriak et al.
Farmatsevtychnyi zhurnal, (1)(1), 70-70 (1980-01-01)
J M Rideout et al.
Clinica chimica acta; international journal of clinical chemistry, 161(1), 29-35 (1986-11-30)
A simple sensitive method for the assay of blood acetaldehyde is described. Samples are collected into an organic solution of 2-diphenylacetyl-1,3-indandione-1-hydrazone. Proteins are precipitated immediately and carbonyl compounds react to form fluorescent azine derivatives. Methanol in the reagent mixture prevents

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