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
Sat Dec 16 01:24:46 UTC 2023
by
admin
on
Sat Dec 16 01:24:46 UTC 2023
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| Record UNII |
S3KFG6Q5X8
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| Record Status |
Validated (UNII)
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947753-66-4
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1311616
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DB11226
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