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Details

Stereochemistry ACHIRAL
Molecular Formula C6H10O3
Molecular Weight 130.1418
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of PROPIONIC ANHYDRIDE

SMILES

CCC(=O)OC(=O)CC

InChI

InChIKey=WYVAMUWZEOHJOQ-UHFFFAOYSA-N
InChI=1S/C6H10O3/c1-3-5(7)9-6(8)4-2/h3-4H2,1-2H3

HIDE SMILES / InChI

Molecular Formula C6H10O3
Molecular Weight 130.1418
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Efficient synthesis, spectral analysis and antimicrobial studies of nitrogen and sulfur containing spiro heterocycles from 2,4-diaryl-3-azabicyclo[3.3.1]nonan-9-ones.
2010-11-15
Investigations on the microbial catabolism of the organic sulfur compounds TDP and DTDP in Ralstonia eutropha H16 employing DNA microarrays.
2010-11
4-Eth-oxy-N'-propanoylpyridine-2-carbohydrazide.
2010-03-27
Characterization of the histone H2A.Z-1 and H2A.Z-2 isoforms in vertebrates.
2009-12-14
N-terminal enrichment: developing a protocol to detect specific proteolytic fragments.
2009-12
The Schizosaccharomyces pombe JmjC-protein, Msc1, prevents H2A.Z localization in centromeric and subtelomeric chromatin domains.
2009-11
Convenient headspace gas chromatographic determination of azide in blood and plasma.
2009-10
Polyethylenimine nanoparticles as an efficient in vitro siRNA delivery system.
2009-09
Effect of acyl chain length on transfection efficiency and toxicity of polyethylenimine.
2009-08-13
Crystalline camptothecin-20(S)-O-propionate hydrate: a novel anticancer agent with strong activity against 19 human tumor xenografts.
2009-06-01
Dynamic Histone H1 Isotype 4 Methylation and Demethylation by Histone Lysine Methyltransferase G9a/KMT1C and the Jumonji Domain-containing JMJD2/KDM4 Proteins.
2009-03-27
High-sensitivity nanoLC-MS/MS analysis of urinary desmosine and isodesmosine.
2009-03-01
3-(Benzimidazolium-2-yl)propionate dihydrate.
2008-10-04
Comprehensive profiling of histone modifications using a label-free approach and its applications in determining structure-function relationships.
2008-09-01
pH memory of immobilized lipase for (+/-)-menthol resolution in ionic liquid.
2008-04-09
Influence of acyl chain length on transfection mediated by acylated PEI nanoparticles.
2007-06-07
Biomass in the manufacture of industrial products--the use of proteins and amino acids.
2007-06
Structure design of multifunctional furoate and pyroglutamate esters of dextran by polymer-analogous reactions.
2007-03-08
Post-translational modifications of histones H3 and H4 associated with the histone methyltransferases Suv39h1 and G9a.
2007
Chemical derivatization of histones for facilitated analysis by mass spectrometry.
2007
Comprehensive phosphoprotein analysis of linker histone H1 from Tetrahymena thermophila.
2006-09
Steric effects in the uncatalyzed and DMAP-catalyzed acylation of alcohols-quantifying the window of opportunity in kinetic resolution experiments.
2006-07-24
High-performance liquid-chromatographic determination of 5-aminosalicylic acid and its metabolites in blood plasma.
2006-06-30
Synthesis of novel (1-alkanoyloxy-4-alkanoylaminobutylidene)-1,1-bisphosphonic acid derivatives.
2006-02-24
N-terminal isotope tagging with propionic anhydride: proteomic analysis of myogenic differentiation of C2C12 cells.
2005-11-05
GC-MS quantitation of codeine, morphine, 6-acetylmorphine, hydrocodone, hydromorphone, oxycodone, and oxymorphone in blood.
2005-08-18
Stereoselective synthesis, structural characterization, and properties of 1,2-O-isopropylidene-3-C-(5-phenyl-1,2,4-oxadiazol-3-yl)-beta-D-psicopyranose.
2005-01-17
Prolonging the action of protein and peptide drugs by a novel approach of reversible polyethylene glycol modification.
2004-09-10
Derivatization for LC-electrospray ionization-MS: a tool for improving reversed-phase separation and ESI responses of bases, ribosides, and intact nucleotides.
2004-05-15
Simultaneous detection and quantitation of morphine, 6-acetylmorphine, and cocaine in toenails: comparison with hair analysis.
2004-03
Investigations on the influence of terminal groups at the C2-propyl side chain of 1,1-bis(4-hydroxyphenyl)-2-phenylpent-1-ene and 1,1,2-tris(4-hydroxyphenyl)pent-1-ene on the estrogen receptor binding and the estrogenic/anti-estrogenic properties.
2003-07
Quantitative determination of rivastigmine and its major metabolite in human plasma by liquid chromatography with atmospheric pressure chemical ionization tandem mass spectrometry.
2003-02-05
Stereoselective synthesis of 1,2:4,5-di-O-isopropylidene-3-C-(5-phenyl-1,2,4-oxadiazol-3-yl)-beta-D-psicopyranose and its X-ray crystallographic analysis.
2003-01-31
Synthesis and biological activities of turkesterone 11alpha-acyl derivatives.
2003
Origin of enantiomeric selectivity in the aryloxyphenoxypropionic acid class of herbicidal acetyl coenzyme A carboxylase (ACCase) inhibitors.
2002-07-31
Quantitative determination of amphetamines, cocaine, and opiates in human hair by gas chromatography/mass spectrometry.
2002-02-18
The acylation of an acyl complex resulting in a labile OCO tridentate ligand.
2002-02-07
Unsymmetrical methylene derivatives of indoles as antiproliferative agents.
2002-01-05
Inhibition of neutrophil O(2)(-) production by unsymmetrical methylene derivatives of benzopyrans: their use as potential antiinflammatory agents.
2002-01-05
A model of the pressure dependence of the enantioselectivity of Candida rugosalipase towards (+/-)-menthol.
2001-10
Acetylcodeine as a marker of illicit heroin in human hair: method validation and results of a pilot study.
2001-03
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:21:00 GMT 2025
Edited
by admin
on Mon Mar 31 19:21:00 GMT 2025
Record UNII
E3A2VV18E6
Record Status Validated (UNII)
Record Version
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Name Type Language
PROPIONIC ANHYDRIDE [HSDB]
Preferred Name English
PROPIONIC ANHYDRIDE
HSDB   MI  
Systematic Name English
PROPIONIC ANHYDRIDE [MI]
Common Name English
Classification Tree Code System Code
EPA PESTICIDE CODE 77704
Created by admin on Mon Mar 31 19:21:00 GMT 2025 , Edited by admin on Mon Mar 31 19:21:00 GMT 2025
DEA NO. 8328
Created by admin on Mon Mar 31 19:21:00 GMT 2025 , Edited by admin on Mon Mar 31 19:21:00 GMT 2025
Code System Code Type Description
CAS
123-62-6
Created by admin on Mon Mar 31 19:21:00 GMT 2025 , Edited by admin on Mon Mar 31 19:21:00 GMT 2025
PRIMARY
ECHA (EC/EINECS)
204-638-2
Created by admin on Mon Mar 31 19:21:00 GMT 2025 , Edited by admin on Mon Mar 31 19:21:00 GMT 2025
PRIMARY
MERCK INDEX
m9210
Created by admin on Mon Mar 31 19:21:00 GMT 2025 , Edited by admin on Mon Mar 31 19:21:00 GMT 2025
PRIMARY Merck Index
FDA UNII
E3A2VV18E6
Created by admin on Mon Mar 31 19:21:00 GMT 2025 , Edited by admin on Mon Mar 31 19:21:00 GMT 2025
PRIMARY
EPA CompTox
DTXSID1027007
Created by admin on Mon Mar 31 19:21:00 GMT 2025 , Edited by admin on Mon Mar 31 19:21:00 GMT 2025
PRIMARY
PUBCHEM
31263
Created by admin on Mon Mar 31 19:21:00 GMT 2025 , Edited by admin on Mon Mar 31 19:21:00 GMT 2025
PRIMARY
HSDB
1215
Created by admin on Mon Mar 31 19:21:00 GMT 2025 , Edited by admin on Mon Mar 31 19:21:00 GMT 2025
PRIMARY
WIKIPEDIA
PROPIONIC ANHYDRIDE
Created by admin on Mon Mar 31 19:21:00 GMT 2025 , Edited by admin on Mon Mar 31 19:21:00 GMT 2025
PRIMARY
Related Record Type Details
PARENT->PRECURSOR