Details
Stereochemistry | ACHIRAL |
Molecular Formula | C10H22O2 |
Molecular Weight | 174.2805 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
OCCCCCCCCCCO
InChI
InChIKey=FOTKYAAJKYLFFN-UHFFFAOYSA-N
InChI=1S/C10H22O2/c11-9-7-5-3-1-2-4-6-8-10-12/h11-12H,1-10H2
Molecular Formula | C10H22O2 |
Molecular Weight | 174.2805 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Approval Year
Conditions
Condition | Modality | Targets | Highest Phase | Product |
---|---|---|---|---|
Inactive ingredient | KLEER-PLEX ADVANCED ACNE CARE SYSTEM Approved UseAcne Treatment.
- For the management of acne.
- Clears up most acne pimples, blackheads, and whiteheads and allows skin to heal.
- Penetrates pores to eliminate most acne blemishes.
- Helps prevent new acne pimples. |
PubMed
Title | Date | PubMed |
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Development and applications of injectable poly(ortho esters) for pain control and periodontal treatment. | 2002 Nov |
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Enzymatic synthesis of multi-component copolymers and their structural characterization. | 2003 |
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Simulating secondary organic aerosol activation by condensation of multiple organics on seed particles. | 2003 Oct 15 |
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Crosslinked poly(methyl vinyl ether-co-maleic anhydride) as topical vehicles for hydrophilic and lipophilic drugs. | 2003 Oct-Dec |
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Crosslinked copolyimide membranes for phenol recovery from process water by pervaporation. | 2003 Sep 15 |
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Use of modified flap structures for study of base excision repair proteins. | 2005 Dec |
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Electrospun fibers of acid-labile biodegradable polymers containing ortho ester groups for controlled release of paracetamol. | 2008 Oct |
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[Bent dsDNA with defined geometric characteristics in terms of complexes of bridged oligonucleotides]. | 2009 May-Jun |
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A self-assembled foldamer capsule: combining single and double helical segments in one aromatic amide sequence. | 2009 Nov 2 |
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Recent advances in synthetic bioelastomers. | 2009 Nov 20 |
|
Synthesis of omega-hydroxy carboxylic acids and alpha,omega-dimethyl ketones using alpha,omega-diols as alkylating agents. | 2010 Mar 5 |
Patents
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 20:12:36 GMT 2023
by
admin
on
Sat Dec 16 20:12:36 GMT 2023
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Record UNII |
5I577UDK52
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Record Status |
Validated (UNII)
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Record Version |
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112-47-0
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17165
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1309235
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5I577UDK52
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m4123
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C118975
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203-975-2
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37153
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5I577UDK52
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DTXSID3059420
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