We have found 46590 results matching your criteria.
Please wait while we search...
  1. 1.
    General Material Information
  2. 2.
    PhysChem Properties
  3. 3.
    Occurrences
  4. 4.
    Organoleptic Properties
  5. 5.
    Suppliers
  6. 6.
    Potential Uses
  7. 7.
    Regulatory & Documentation
  8. 8.
    Safety Information
  9. 9.
    Other Information
  10. 10.
    Blenders & Components
  11. 11.
    Literature & References

4-benzoyl pyridine

Chemical Structure

General Material Information

Preferred name 4-benzoyl pyridine
Trivial Name 4-Benzoylpyridine
Short Description pyridine, 4-benzoyl-
Formula C12 H9 N O
CAS Number 14548-46-0
ECHA Number 238-586-7
FDA UNII 524YQ3O21T
Nikkaji Number J15.003G
Beilstein Number 0003864
MDL MFCD00006430
Bio Activity Summary External link
NMR Predictor External link
Synonyms
  • gamma- benzoyl pyridine
  • 4-benzoylpyridine
  • gamma- benzoylpyridine
  • ketone, phenyl 4-pyridyl
  • methanone, phenyl-4-pyridinyl-
  • phenyl (4-pyridinyl) methanone
  • phenyl 4-pyridyl ketone
  • phenyl-4-pyridinylmethanone
  • phenyl-pyridin-4-yl-methanone
  • phenyl(4-pyridinyl)methanone
  • phenyl(pyridin-4-yl)methanone
  • pyridine, 4-benzoyl-
  • 4-pyridyl phenyl ketone
  • 4-Pyridyl phenyl ketone
  • 4-Benzoylpyridine
  • Ba 33215
  • γ-Benzoylpyridine
  • NSC 9488

US / EU / FDA / JECFA / FEMA / Scholar / Patents

Google Scholar Start search
Google Books Start search
Google Patents Start search
Perfumer & Flavorists Start search
EU Patents Start search
PubMeb Start search
NCBI Start search

Literature & References

phenyl(pyridin-4-yl)methanone
NIST Chemistry WebBook:Search Inchi
Pubchem (cid):26731
Pubchem (sid):134991205
Publications by US Patents
3,952,024 - Furfurylthioacetone
Certain 2,5-dimethyl-3-thiopyrazines
Publications by PubMed
Photoinduced Oxidation of Secondary Alcohols Using 4-Benzoylpyridine as an Oxidant.
Generation of free oxygen atoms O((3)P) in solution by photolysis of 4-benzoylpyridine N-oxide.
Synthesis, structure, spectral, thermal and first-order molecular hyperpolarizability of 4-benzoylpyridine isonicotinyl hydrazone monohydrate single crystals.
Two copper(II) complexes with 4-benzoylpyridine ligand: synthesis, crystal structure and luminescent properties.
Comparative inhibition of tetrameric carbonyl reductase activity in pig heart cytosol by alkyl 4-pyridyl ketones.
S-nitrosoglutathione covalently modifies cysteine residues of human carbonyl reductase 1 and affects its activity.
Studies on the 4-benzoylpyridine-3-carboxamide entity as a fragment model of the Isoniazid-NAD adduct.
Stereoselective reduction of 4-benzoylpyridine in the heart of vertebrates.
9,10-phenanthrenequinone, a component of diesel exhaust particles, inhibits the reduction of 4-benzoylpyridine and all-trans-retinal and mediates superoxide formation through its redox cycling in pig heart.
Towards the chemical control of molecular packing: syntheses and crystal structures of three trans-[NiL4(NCS)2] complexes.
Possible mechanism of superoxide formation through redox cycling of plumbagin in pig heart.
Different topologies in three manganese-μ-azido 1D compounds: magnetic behavior and DFT-quantum Monte Carlo calculations.
Rhenium-to-benzoylpyridine and rhenium-to-bipyridine MLCT excited states of fac-[Re(Cl)(4-benzoylpyridine)(2)(CO)(3)] and fac-[Re(4-benzoylpyridine)(CO)(3)(bpy)](+): a time-resolved spectroscopic and spectroelectrochemical study.
Two new one-dimensional compounds with end-to-end dicyanamide as a bridging ligand: syntheses and structural characterization of trans-[Mn(4-bzpy)2(N(CN)2)2]n and cis-[Mn(Bpy)(N(CN)2)2]n, (4-bzpy = 4-benzoylpyridine; bpy = 2,2'-bipyridyl).
Excited-state characteristics of tetracyanidonitridorhenium(V) and -technetium(V) complexes with N-heteroaromatic ligands.
Interindividual variability of carbonyl reductase levels in human livers.
Involvement of carbonyl reductase in superoxide formation through redox cycling of adrenochrome and 9,10-phenanthrenequinone in pig heart.
Inhibitory effects of flavonoids on rabbit heart carbonyl reductase.
Purification and catalytic properties of a tetrameric carbonyl reductase from rabbit heart.
Immunohistochemical localization and physiological regulation of carbonyl reductase in immature rat ovary.
Structural combination of established 5-HT(2A) receptor ligands: new aspects of the binding mode.
[Structure and function of peroxisomal tetrameric carbonyl reductase].
Luminescence ranging from red to blue: a series of copper(I)-halide complexes having rhombic {Cu2(mu-X)2} (X = Br and I) units with N-heteroaromatic ligands.
Inhibition of rabbit heart carbonyl reductase by fatty acids.
Characterization of multiple forms of carbonyl reductase from chicken liver.
Effects of antiestrogens on ovarian aldo-keto reductase in relation to ovulation in rats.
Regulation of ovarian carbonyl reductase mediated by estrogen receptor in immature rats.
Carbonyl reductases from rat testis and vas deferens. Purification, properties and localization.
Different functions between human monomeric carbonyl reductase 3 and carbonyl reductase 1.
Inhibition of carbonyl reductase activity in pig heart by alkyl phenyl ketones.
Differences in catalytic activity between rat testicular and ovarian carbonyl reductases are due to two amino acids.
Characterization of multiple Chinese hamster carbonyl reductases.
Pre- and post-ovulatory changes in carbonyl reductase in ovarian follicles and corpora lutea in rats.
Carbonyl reductase activity exhibited by pig testicular 20 beta-hydroxysteroid dehydrogenase.
Inhibition of pink color development in cooked, uncured ground turkey through the binding of non-pink generating ligands to muscle pigments.
Effects of psychotropic drugs on aldo-keto reductase activity in rat ovary and adrenal gland.
Purification and characterization of 5 alpha-dihydrotestosterone 3 beta-hydroxysteroid dehydrogenase from mature pig testicular cytosol.
Structural requirements for the induction of hepatic microsomal cytochrome P450 by imidazole- and pyridine-containing compounds in rats.
Changes and localization of ovarian carbonyl reductase during pseudopregnancy and pregnancy in rats.
Physiological role of ovarian carbonyl reductase and effect of antiestrogen on its activity in rats.
Kinetic mechanisms in the reduction of aldehydes and ketones catalyzed by rabbit liver aldehyde reductases and hydroxysteroid dehydrogenases.

Other Information

(IUPAC):Atomic Weights of the Elements 2011 (pdf)
Videos:The Periodic Table of Videos
tgsc:Atomic Weights use for this web site
(IUPAC):Periodic Table of the Elements
CHEMBL:View
HMDB (The Human Metabolome Database):Search
Export Tariff Code:2933.39.9100
ChemSpider:View

PhysChem Properties

Material listed in food chemical codex No
Molecular weight 183.20993041992
Boiling Point 130 to 131°C @ 1 mm Hg
Flash Point TCC Value 150 °C TCC
logP (o/w) 1.98
Solubility
alcohol Yes
water, 1082 mg/L @ 25 °C (est) Yes
water No

Safety Information

Safety information

Preferred SDS: View
Hazards identification
Classification of the substance or mixture
GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)
None found.
GHS Label elements, including precautionary statements
Pictogram
Hazard statement(s)
None found.
Precautionary statement(s)
None found.
Oral/Parenteral Toxicity:
intraperitoneal-mouse LD50 520 mg/kg
Journal of Medicinal Chemistry. Vol. 14, Pg. 551, 1971.

Dermal Toxicity:
Not determined
Inhalation Toxicity:
Not determined

Safety in use information

Category:
information only not used for fragrances or flavors
Recommendation for 4-benzoyl pyridine usage levels up to:
not for fragrance use.
Recommendation for 4-benzoyl pyridine flavor usage levels up to:
not for flavor use.

Safety references

EPI System: View
AIDS Citations:Search
Cancer Citations:Search
Toxicology Citations:Search
EPA Substance Registry Services (TSCA):14548-46-0
EPA ACToR:Toxicology Data
EPA Substance Registry Services (SRS):Registry
Laboratory Chemical Safety Summary :26731
National Institute of Allergy and Infectious Diseases:Data
WGK Germany:3
phenyl(pyridin-4-yl)methanone
Chemidplus:0014548460
RTECS:OB6402000 for cas# 14548-46-0