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Sigma-Aldrich

1-Phenyl-3-pyrazolidinone

97%

Synonym(s):

Phenidone

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About This Item

Empirical Formula (Hill Notation):
C9H10N2O
CAS Number:
92-43-3
Molecular Weight:
162.19
Beilstein:
131856
EC Number:
202-155-1
MDL number:
MFCD00003094
UNSPSC Code:
12352100
PubChem Substance ID:
24847805
NACRES:
NA.22

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)

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Related Categories

Application

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

Pictograms

Exclamation markEnvironment
GHS07,GHS09

Signal Word

Warning

Hazard Statements

H302,H411

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Chronic 2

Storage Class Code

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

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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)
Monika Frey et al.
Phytochemistry, 65(8), 1047-1055 (2004-04-28)
The indole-3-glycerol phosphate lyase Igl is the structural gene of volatile indole biosynthesis in the tritrophic interaction in maize. The gene is activated on transcriptional level with the same kinetics and to the same level by the fatty acid-amino acid
J Peng et al.
Plant biology (Stuttgart, Germany), 13(2), 276-284 (2011-02-12)
When attacked by herbivores, plants release herbivore-induced plant volatiles (HIPV) that may function in direct defence by repelling herbivores or reducing their growth. Emission of HIPV may also contribute to indirect defence by attracting natural enemies of the herbivore. Here
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
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