Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C25H29NO3 |
| Molecular Weight | 391.5027 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 1 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCCCC(CC)COC(=O)C(C#N)=C(C1=CC=CC=C1)C2=CC=C(OC)C=C2
InChI
InChIKey=WAJCJDLRJVDSSD-WCWDXBQESA-N
InChI=1S/C25H29NO3/c1-4-6-10-19(5-2)18-29-25(27)23(17-26)24(20-11-8-7-9-12-20)21-13-15-22(28-3)16-14-21/h7-9,11-16,19H,4-6,10,18H2,1-3H3/b24-23+
| Molecular Formula | C25H29NO3 |
| Molecular Weight | 391.5027 |
| Charge | 0 |
| Count |
|
| Stereochemistry | RACEMIC |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 1 |
| Optical Activity | ( + / - ) |
ETHYLHEXYL METHOXYCRYLENE, an effective photostabilizer for certain organic UV absorbers such as avobenzone and octyl methoxycinnamate, absorbs in the UV-A region. It is an outstanding solvent for crystalline UV filters, is easily emulsified, and is suitable for use in lotion, cream, spray, stick, and gel formulations in skin care and sun care products.
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 20:49:34 GMT 2025
by
admin
on
Mon Mar 31 20:49:34 GMT 2025
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| Record UNII |
S3KFG6Q5X8
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| Record Status |
Validated (UNII)
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| Record Version |
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S3KFG6Q5X8
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DB11226
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admin on Mon Mar 31 20:49:34 GMT 2025 , Edited by admin on Mon Mar 31 20:49:34 GMT 2025
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