127914
1-Phenyl-3-pyrazolidinone
97%
Synonym(s):
Phenidone
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All Photos(2)
About This Item
Empirical Formula (Hill Notation):
C9H10N2O
CAS Number:
Molecular Weight:
162.19
Beilstein:
131856
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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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)
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Application
1-Phenyl-3-pyrazolidinone was used as a photograph developing agent.
Signal Word
Warning
Hazard Statements
Precautionary Statements
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
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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)
J C Bedick et al.
Comparative biochemistry and physiology. Toxicology & pharmacology : CBP, 130(1), 107-117 (2001-09-07)
Nodulation is the first, and qualitatively predominant, cellular defense reaction to bacterial infections in insects. We tested the hypothesis that eicosanoids also mediate nodulation reactions to bacterial challenge in adults of a social insect, the honey bee, Apis mellifera. Treating
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
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
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