Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C10H13NO4 |
| Molecular Weight | 211.2145 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
NC1=CC=C(C=C1)C(=O)OCC(O)CO
InChI
InChIKey=WHQOKFZWSDOTQP-UHFFFAOYSA-N
InChI=1S/C10H13NO4/c11-8-3-1-7(2-4-8)10(14)15-6-9(13)5-12/h1-4,9,12-13H,5-6,11H2
| Molecular Formula | C10H13NO4 |
| Molecular Weight | 211.2145 |
| Charge | 0 |
| Count |
|
| Stereochemistry | RACEMIC |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Optical Activity | ( + / - ) |
Lisadimate (glyceryl PABA), a substituted aminobenzoate, is a sunscreen with actions similar to those of aminobenzoic acid. It is effective against UVB light. Glyceryl PABA (Escalol 106), present in many popular sunscreens, is a common sensitizer which invariably cross-reacts with benzocaine; it is present in over 400 over-the-counter products. Glyceryl PABA does not appear to cross-react with the sunscreening agents amyl (Escalol 506) and octyl (Escalol 507) dimethyl PABA. Glyceryl PABA, may, on occasion, cross-react with para-aminobenzoic acid (PABA), paraphenylenediamine, aniline, and sulfa drugs. Ironically, the sunscreening agent glyceryl PABA may, itself, act as a photosensitizing agent.
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Wed Apr 02 09:05:12 GMT 2025
by
admin
on
Wed Apr 02 09:05:12 GMT 2025
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| Record UNII |
A886B5N5IM
|
| Record Status |
Validated (UNII)
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| Record Version |
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-
Download
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Preferred Name | English | ||
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Official Name | English | ||
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Common Name | English | ||
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| Classification Tree | Code System | Code | ||
|---|---|---|---|---|
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NCI_THESAURUS |
C851
Created by
admin on Wed Apr 02 09:05:12 GMT 2025 , Edited by admin on Wed Apr 02 09:05:12 GMT 2025
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EPA PESTICIDE CODE |
9102
Created by
admin on Wed Apr 02 09:05:12 GMT 2025 , Edited by admin on Wed Apr 02 09:05:12 GMT 2025
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| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
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BB-100
Created by
admin on Wed Apr 02 09:05:12 GMT 2025 , Edited by admin on Wed Apr 02 09:05:12 GMT 2025
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8692
Created by
admin on Wed Apr 02 09:05:12 GMT 2025 , Edited by admin on Wed Apr 02 09:05:12 GMT 2025
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6627
Created by
admin on Wed Apr 02 09:05:12 GMT 2025 , Edited by admin on Wed Apr 02 09:05:12 GMT 2025
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CHEMBL2106668
Created by
admin on Wed Apr 02 09:05:12 GMT 2025 , Edited by admin on Wed Apr 02 09:05:12 GMT 2025
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100000082524
Created by
admin on Wed Apr 02 09:05:12 GMT 2025 , Edited by admin on Wed Apr 02 09:05:12 GMT 2025
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205-244-3
Created by
admin on Wed Apr 02 09:05:12 GMT 2025 , Edited by admin on Wed Apr 02 09:05:12 GMT 2025
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PRIMARY | |||
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m5793
Created by
admin on Wed Apr 02 09:05:12 GMT 2025 , Edited by admin on Wed Apr 02 09:05:12 GMT 2025
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PRIMARY | Merck Index | ||
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DTXSID8042002
Created by
admin on Wed Apr 02 09:05:12 GMT 2025 , Edited by admin on Wed Apr 02 09:05:12 GMT 2025
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SUB08532MIG
Created by
admin on Wed Apr 02 09:05:12 GMT 2025 , Edited by admin on Wed Apr 02 09:05:12 GMT 2025
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A886B5N5IM
Created by
admin on Wed Apr 02 09:05:12 GMT 2025 , Edited by admin on Wed Apr 02 09:05:12 GMT 2025
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PRIMARY | |||
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C76109
Created by
admin on Wed Apr 02 09:05:12 GMT 2025 , Edited by admin on Wed Apr 02 09:05:12 GMT 2025
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136-44-7
Created by
admin on Wed Apr 02 09:05:12 GMT 2025 , Edited by admin on Wed Apr 02 09:05:12 GMT 2025
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PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
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ENANTIOMER -> RACEMATE | |||
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ENANTIOMER -> RACEMATE |
| Related Record | Type | Details | ||
|---|---|---|---|---|
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ACTIVE MOIETY |