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Details

Stereochemistry ACHIRAL
Molecular Formula C4H8O2
Molecular Weight 88.1051
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of Dioxane

SMILES

C1COCCO1

InChI

InChIKey=RYHBNJHYFVUHQT-UHFFFAOYSA-N
InChI=1S/C4H8O2/c1-2-6-4-3-5-1/h1-4H2

HIDE SMILES / InChI

Molecular Formula C4H8O2
Molecular Weight 88.1051
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Physico-chemical studies on the charge-transfer complex formed between sulfadoxine and pyrimethamine with chloranilic acid.
2002-07-20
A new synthetic route to boron-10 enriched pentaborane(9) from boric acid and its conversion to anti-(10)B(18)H(22).
2002-06-26
Fluorescence probe properties of intramolecular charge transfer diphenylbutadienes in micelles and vesicles.
2002-06-13
N,N'-Dithiobisphthalimide-1,4-dioxan (1/0.6): a C2/c solvate with disordered solvent molecules localized in channels.
2002-06
Crystallization and preliminary diffraction data of BaP1, a haemorrhagic metalloproteinase from Bothrops asper snake venom.
2002-06
Effect of blending calcium compounds on hydrolytic degradation of poly(DL-lactic acid-co-glycolic acid).
2002-06
13C-NMR study of 4-azasteroids in solution and solid state.
2002-06
Electronic effects and the stereochemistries in rearrangement-displacement reactions of triaryl(halomethyl)silanes with fluoride and with alkoxide ions.
2002-05-31
The rodent carcinogens 1,4-dioxane and thiourea induce meiotic non-disjunction in Drosophila melanogaster females.
2002-05-27
Optimization of the separation of some Chelidonium maius L. alkaloids by reversed phase high-performance liquid chromatography using cyanopropyl bonded stationary phase.
2002-05-25
Syntheses of C12,N13 heterocyclic bridged fused indenopyrrolocarbazoles.
2002-05-17
Molecular imprinting of enzymes with water-insoluble ligands for nonaqueous biocatalysis.
2002-05-15
Design and synthesis of novel 5-substituted acyclic pyrimidine nucleosides as potent and selective inhibitors of hepatitis B virus.
2002-05-09
A study of the ionic liquid mediated microwave heating of organic solvents.
2002-05-03
Improved synthesis and molecular modeling of 4beta,19-dihydroxyandrost-5-en-17-one, an excellent inhibitor of aromatase.
2002-05
Determination of the retention behavior of barbituric acid derivatives in reversed-phase high-performance liquid chromatography by using quantitative structure-retention relationships.
2002-04-25
Selective permeation and organic extraction of recombinant green fluorescent protein (gfpuv) from Escherichia coli.
2002-04-24
Coupling of surface carboxyls of carboxymethylcellulase with aniline via chemical modification: extreme thermostabilization in aqueous and water-miscible organic mixtures.
2002-04-06
Enzyme activation in organic solvents: co-lyophilization of subtilisin Carlsberg with methyl-beta-cyclodextrin renders an enzyme catalyst more active than the cross-linked enzyme crystals.
2002-04-05
Collagen stability: insights from NMR spectroscopic and hybrid density functional computational investigations of the effect of electronegative substituents on prolyl ring conformations.
2002-03-20
Second derivative fluorescence spectra of indole compounds.
2002-03
Crystallization and X-ray analysis of native and selenomethionyl beta-mannanase Man5A from blue mussel, Mytilus edulis, expressed in Pichia pastoris.
2002-03
Inclusion behavior of thiacalix[4]arenetetrasulfonate toward water-miscible organic molecules studied by salting-out and X-ray crystallography.
2002-02-21
Pd(II) acts simultaneously as a Lewis acid and as a transition-metal catalyst: synthesis of cyclic alkenyl ethers from acetylenic aldehydes.
2002-02-06
New organic superconductors consisting of an unprecedented pi-electron donor.
2002-02-06
Enzymatic synthesis of a capsinoid by the acylation of vanillyl alcohol with fatty acid derivatives catalyzed by lipases.
2002-02
2,3,6,7-Tetrahydroxy-9,10-dimethyl-9,10-dihydro-9,10-ethanoanthracene bis(1,4-dioxane) solvate.
2002-02
Effect of organic solvents on stability and activity of two related alcohol dehydrogenases: a comparative study.
2002-02
Antifungal sordarins. Synthesis and structure-activity relationships of 3',4'-fused dioxolane and dioxane derivatives.
2002-01-21
Synthesis of alternating polystyrene/poly(ethyleneoxide) branched polymacromonomers.
2002-01-18
Solvent effects on the electronic absorption spectra and acid strength of some substituted pyridinols.
2002-01-15
Synthesis of alpha-lactosyl-(1-->3)-L-glycero-alpha-D-manno-heptopyranoside, a partial oligosaccharide structure expressed within the lipooligosaccharide produced by Neisseria gonorrhoeae strain 15253.
2002-01-07
Excited state proton transfer reaction of two new intramolecularly hydrogen bonded Schiff bases at room temperature and 77K.
2002-01-01
Macroporous poly(L-lactide) scaffold 1. Preparation of a macroporous scaffold by liquid--liquid phase separation of a PLLA--dioxane--water system.
2002
Reversible fixation of carbon dioxide at nickel(0) centers: a route for large organometallic rings, dimers, and tetramers.
2001-12-03
Quenching of singlet molecular oxygen (1O2) by azide anion in solvent mixtures.
2001-12
A laser flash photolysis study of curcumin in dioxane-water mixtures.
2001-12
Synthesis and in vitro antifungal activities of novel triazole antifungal agent CS-758.
2001-12
Mechanisms of acid-catalyzed Z/E isomerization of imines.
2001-11-30
Preparation of 1-(3-C-(propa-1,2-dienyl)-D-ribo-pentofuranosyl)uracil, an allenic nucleoside.
2001-11-27
1,4-dioxane-fused 4-anilinoquinazoline as inhibitors of epidermal growth factor receptor kinase.
2001-11
Two OPEEs (organic phase enzyme electrodes) used to check the percentage water content in hydrophobic foods and drugs.
2001-11
Enantioselective ring cleavage of dioxane acetals mediated by a chiral Lewis acid: application to asymmetric desymmetrization of meso-1,3-diols.
2001-10-18
[Development of aziridination and azetizination reactions of amino allenes using a palladium catalyst].
2001-10
Fast, efficient and selective deprotection of the tert-butoxycarbonyl (Boc) group using HCl/dioxane (4 m).
2001-10
Effects of liquid phase composition on salt cluster formation in positive ion mode electrospray mass spectrometry: implications for clustering mechanism in electrospray.
2001-10
Effect of chronic inhalation of toluene and dioxane on activity of free radical processes in rat ovaries and brain.
2001-09
Interpretation of the reversible inhibition of adenosine deaminase by small cosolutes in terms of molecular crowding.
2001-08-14
Crystallization and preliminary X-ray analysis of human transglutaminase 3 from zymogen to active form.
2001-07
Final report on the safety assessment of PEG-25 propylene glycol stearate, PEG-75 propylene glycol stearate, PEG-120 propylene glycol stearate, PEG-10 propylene glycol, PEG-8 propylene glycol cocoate, and PEG-55 propylene glycol oleate.
2001
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 17:34:19 GMT 2025
Edited
by admin
on Mon Mar 31 17:34:19 GMT 2025
Record UNII
J8A3S10O7S
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
1,4-DIOXANE
HSDB  
Preferred Name English
Dioxane
MI  
Systematic Name English
DIOXAN [MART.]
Common Name English
1,4-DIOXANE [USP-RS]
Common Name English
1,4-DIOXANE [IARC]
Common Name English
DIOXANE [MI]
Common Name English
NSC-8728
Code English
1,4-DIOXANE [HSDB]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C45187
Created by admin on Mon Mar 31 17:34:19 GMT 2025 , Edited by admin on Mon Mar 31 17:34:19 GMT 2025
Code System Code Type Description
DAILYMED
J8A3S10O7S
Created by admin on Mon Mar 31 17:34:19 GMT 2025 , Edited by admin on Mon Mar 31 17:34:19 GMT 2025
PRIMARY
EVMPD
SUB130313
Created by admin on Mon Mar 31 17:34:19 GMT 2025 , Edited by admin on Mon Mar 31 17:34:19 GMT 2025
PRIMARY
HSDB
81
Created by admin on Mon Mar 31 17:34:19 GMT 2025 , Edited by admin on Mon Mar 31 17:34:19 GMT 2025
PRIMARY
RXCUI
2383534
Created by admin on Mon Mar 31 17:34:19 GMT 2025 , Edited by admin on Mon Mar 31 17:34:19 GMT 2025
PRIMARY
RS_ITEM_NUM
1601521
Created by admin on Mon Mar 31 17:34:19 GMT 2025 , Edited by admin on Mon Mar 31 17:34:19 GMT 2025
PRIMARY
WIKIPEDIA
1,4-DIOXANE
Created by admin on Mon Mar 31 17:34:19 GMT 2025 , Edited by admin on Mon Mar 31 17:34:19 GMT 2025
PRIMARY
PUBCHEM
31275
Created by admin on Mon Mar 31 17:34:19 GMT 2025 , Edited by admin on Mon Mar 31 17:34:19 GMT 2025
PRIMARY
CHEBI
46923
Created by admin on Mon Mar 31 17:34:19 GMT 2025 , Edited by admin on Mon Mar 31 17:34:19 GMT 2025
PRIMARY
DRUG BANK
DB03316
Created by admin on Mon Mar 31 17:34:19 GMT 2025 , Edited by admin on Mon Mar 31 17:34:19 GMT 2025
PRIMARY
MERCK INDEX
m4598
Created by admin on Mon Mar 31 17:34:19 GMT 2025 , Edited by admin on Mon Mar 31 17:34:19 GMT 2025
PRIMARY Merck Index
EPA CompTox
DTXSID4020533
Created by admin on Mon Mar 31 17:34:19 GMT 2025 , Edited by admin on Mon Mar 31 17:34:19 GMT 2025
PRIMARY
CHEBI
47032
Created by admin on Mon Mar 31 17:34:19 GMT 2025 , Edited by admin on Mon Mar 31 17:34:19 GMT 2025
PRIMARY
SMS_ID
100000156409
Created by admin on Mon Mar 31 17:34:19 GMT 2025 , Edited by admin on Mon Mar 31 17:34:19 GMT 2025
PRIMARY
ECHA (EC/EINECS)
204-661-8
Created by admin on Mon Mar 31 17:34:19 GMT 2025 , Edited by admin on Mon Mar 31 17:34:19 GMT 2025
PRIMARY
NSC
8728
Created by admin on Mon Mar 31 17:34:19 GMT 2025 , Edited by admin on Mon Mar 31 17:34:19 GMT 2025
PRIMARY
FDA UNII
J8A3S10O7S
Created by admin on Mon Mar 31 17:34:19 GMT 2025 , Edited by admin on Mon Mar 31 17:34:19 GMT 2025
PRIMARY
CAS
123-91-1
Created by admin on Mon Mar 31 17:34:19 GMT 2025 , Edited by admin on Mon Mar 31 17:34:19 GMT 2025
PRIMARY
MESH
C025223
Created by admin on Mon Mar 31 17:34:19 GMT 2025 , Edited by admin on Mon Mar 31 17:34:19 GMT 2025
PRIMARY
NCI_THESAURUS
C44298
Created by admin on Mon Mar 31 17:34:19 GMT 2025 , Edited by admin on Mon Mar 31 17:34:19 GMT 2025
PRIMARY NCIT
Related Record Type Details
METABOLITE -> PARENT
Related Record Type Details
PARENT -> IMPURITY
Limit of Residual Solvents
CHROMATOGRAPHIC PURITY (GC)
USP