Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C12H24O2 |
| Molecular Weight | 200.3178 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCCCCCCCCC1OCCO1
InChI
InChIKey=QPILHXCDZYWYLQ-UHFFFAOYSA-N
InChI=1S/C12H24O2/c1-2-3-4-5-6-7-8-9-12-13-10-11-14-12/h12H,2-11H2,1H3
| Molecular Formula | C12H24O2 |
| Molecular Weight | 200.3178 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Enhanced econazole penetration into human nail by 2-n-nonyl-1,3-dioxolane. | 2003 Jan |
|
| Feline penile erection induced by topical glans penis application of combination alprostadil and SEPA (Topiglan). | 2004 Feb |
|
| Amphiphilic transdermal permeation enhancers: structure-activity relationships. | 2005 |
|
| Mechanisms of action of novel skin penetration enhancers: phospholipid versus skin lipid liposomes. | 2005 Nov 23 |
|
| [Effects of 2-n-nonyl-1,3-dioxolane as an enhanceron transdermal absorption of Salvia miltiorrhiza gel]. | 2007 Mar |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 05:43:03 GMT 2023
by
admin
on
Sat Dec 16 05:43:03 GMT 2023
|
| Record UNII |
Z1S2N84X7X
|
| Record Status |
Validated (UNII)
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| Record Version |
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224-422-1
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m8037
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6620
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78056
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