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Merck
CN

127914

1-Phenyl-3-pyrazolidinone

97%

Synonym(s):

Phenidone

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About This Item

Empirical Formula (Hill Notation):
C9H10N2O
CAS Number:
Molecular Weight:
162.19
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
202-155-1
Beilstein/REAXYS Number:
131856
MDL number:
Assay:
97%
Form:
powder
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Quality Level

assay

97%

form

powder

mp

119-121 °C (lit.)

SMILES string

O=C1CCN(N1)c2ccccc2

InChI

1S/C9H10N2O/c12-9-6-7-11(10-9)8-4-2-1-3-5-8/h1-5H,6-7H2,(H,10,12)

InChI key

CMCWWLVWPDLCRM-UHFFFAOYSA-N

Gene Information

rat ... Alox5(25290)

Application

1-Phenyl-3-pyrazolidinone was used as a photograph developing agent.


pictograms

Exclamation markEnvironment

signalword

Warning

hcodes

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Chronic 2

Storage Class

11 - Combustible Solids

wgk

WGK 2

flash_point_f

275.5 °F - Pensky-Martens closed cup

flash_point_c

135.3 °C - Pensky-Martens closed cup

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves



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The Oxidation of 1-Phenyl-4, 4-dimethyl-3-pyrazolidinone in Alkaline Solution.
The Journal of Organic Chemistry, 30(8), 2571-2575 (1965)
Venkatesan Radhika et al.
PloS one, 5(2), e9265-e9265 (2010-02-23)
Plants produce nectar in their flowers as a reward for their pollinators and most of our crops depend on insect pollination, but little is known on the physiological control of nectar secretion. Jasmonates are well-known for their effects on senescence
Eun-Seon Kim et al.
Plant molecular biology, 52(6), 1203-1213 (2003-12-20)
Lipoxygenases (LOXs) catalyze the formation of fatty acid hydroperoxides involved in responses to stresses. This study examines the expression of a non-traditional dual positional specific maize LOX in response to wounding or methyl jasmonate (MeJA). Full-length maize LOX cDNA was



Global Trade Item Number

SKUGTIN
127914-25G04061838725257
127914-100G04061838725240