Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C7H14O2 |
| Molecular Weight | 130.1849 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCCCOCC1CO1
InChI
InChIKey=YSUQLAYJZDEMOT-UHFFFAOYSA-N
InChI=1S/C7H14O2/c1-2-3-4-8-5-7-6-9-7/h7H,2-6H2,1H3
| Molecular Formula | C7H14O2 |
| Molecular Weight | 130.1849 |
| Charge | 0 |
| Count |
|
| Stereochemistry | RACEMIC |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Optical Activity | ( + / - ) |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Genes specifically modulated in sensitized skins allow the detection of sensitizers in a reconstructed human skin model. Development of the SENS-IS assay. | 2015-06 |
|
| Reduced sensitizing capacity of epoxy resin systems: a structure-activity relationship study. | 2009-11 |
|
| Do uric acid deposits in zooxanthellae function as eye-spots? | 2009-07-17 |
|
| Metabolism and disposition of n-butyl glycidyl ether in F344 rats and B6C3F1 mice. | 2007-12 |
|
| The effect of chemical modification of amino acid side-chains on collagen degradation by enzymes. | 2007-04 |
|
| Modulation of collagen proteolysis by chemical modification of amino acid side-chains in acellularized arteries. | 2004-05 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 23:10:16 GMT 2025
by
admin
on
Mon Mar 31 23:10:16 GMT 2025
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| Record UNII |
M03777A62S
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| Record Status |
Validated (UNII)
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| Record Version |
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| Code System | Code | Type | Description | ||
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100000159557
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83413
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17049
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2426-08-6
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DTXSID9024691
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SUB169813
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219-376-4
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n-Butyl glycidyl ether
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299
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M03777A62S
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| Related Record | Type | Details | ||
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ENANTIOMER -> RACEMATE | |||
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ENANTIOMER -> RACEMATE |
