Details
Stereochemistry | ACHIRAL |
Molecular Formula | C18H30N2O2 |
Molecular Weight | 306.443 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CCCCN(CCCC)CCCOC(=O)C1=CC=C(N)C=C1
InChI
InChIKey=HQFWVSGBVLEQGA-UHFFFAOYSA-N
InChI=1S/C18H30N2O2/c1-3-5-12-20(13-6-4-2)14-7-15-22-18(21)16-8-10-17(19)11-9-16/h8-11H,3-7,12-15,19H2,1-2H3
Molecular Formula | C18H30N2O2 |
Molecular Weight | 306.443 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
DescriptionSources: https://www.ncbi.nlm.nih.gov/pubmed/12174527
Sources: https://www.ncbi.nlm.nih.gov/pubmed/12174527
Butacaine is a local anesthetic. It should not be used with people who have a history of allergies due to the possibility of anaphylactic shock.
Approval Year
PubMed
Title | Date | PubMed |
---|---|---|
Keratitis from misuse of corneal anesthetics. | 1968 Aug 22 |
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Selective dopaminergic vulnerability: 3,4-dihydroxyphenylacetaldehyde targets mitochondria. | 2001 Apr 15 |
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Managing patients with local anesthetic complications using alternative methods. | 2002 May-Jun |
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PAMPA - excipient classification gradient map. | 2006 Nov |
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Solubility-excipient classification gradient maps. | 2007 Mar |
Patents
Sample Use Guides
In Vitro Use Guide
Sources: http://www.ncbi.nlm.nih.gov/pubmed/6240271
The specific activities of two transferases, aspartate-amino-transferase and creatine phosphokinase, are increased by 10(-5) mol/l butacaine
Substance Class |
Chemical
Created
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admin
on
Edited
Fri Dec 15 16:24:02 GMT 2023
by
admin
on
Fri Dec 15 16:24:02 GMT 2023
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Record UNII |
Z84S23CGJJ
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Record Status |
Validated (UNII)
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NCI_THESAURUS |
C245
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CFR |
21 CFR 524.1580C
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C87457
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758632
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DB11502
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m2780
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Z84S23CGJJ
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BUTACAINE
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2480
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DTXSID3045300
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SUB05994MIG
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149-16-6
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1829
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3050
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Related Record | Type | Details | ||
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SALT/SOLVATE -> PARENT |
Related Record | Type | Details | ||
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ACTIVE MOIETY |