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Details

Stereochemistry ACHIRAL
Molecular Formula C17H27NO3
Molecular Weight 293.4012
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of EMBUTRAMIDE

SMILES

CCC(CC)(CNC(=O)CCCO)C1=CC=CC(OC)=C1

InChI

InChIKey=LMBMDLOSPKIWAP-UHFFFAOYSA-N
InChI=1S/C17H27NO3/c1-4-17(5-2,13-18-16(20)10-7-11-19)14-8-6-9-15(12-14)21-3/h6,8-9,12,19H,4-5,7,10-11,13H2,1-3H3,(H,18,20)

HIDE SMILES / InChI

Molecular Formula C17H27NO3
Molecular Weight 293.4012
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Description
Curator's Comment: description was created based on several sources, including, www.ncbi.nlm.nih.gov/pubmed/27404634

Embutramide is a veterinary, CNS active medicine used for euthanasia in dogs. The drug is marketed under the name Tributame in the USA and under the name Tanax in Europe. Human consumption of the drug is usually associated with suicide attempts.

Approval Year

Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Palliative
TRIBUTAME

Approved Use

TRIBUTAME Euthanasia Solution is indicated for euthanasia in dogs only.

Launch Date

2005
PubMed

PubMed

TitleDatePubMed
Dimethylformamide metabolism following self-harm using a veterinary euthanasia product.
2010-08
Dorsal arthrodesis in prepubertal New Zealand white rabbits followed to skeletal maturity: Effect on thoracic dimensions, spine growth and neural elements.
2010-01
Different solutions used for submucosal injection influenced early healing of gastric endoscopic mucosal resection in a preclinical study in experimental pigs.
2009-09
Prothrombin complex concentrate vs fresh frozen plasma for reversal of dilutional coagulopathy in a porcine trauma model.
2009-03
Experimental infection with a low virulence isolate of Neospora caninum at 70 days gestation in cattle did not result in foetopathy.
2009-02-27
Development of a liquid chromatography-tandem mass spectrometry method for an euthanasic veterinarian drug: Tanax.
2008-11-04
Effects of electromagnetic fields of low frequency and low intensity on rat metabolism.
2008-04-01
DEA lists embutramide as schedule III controlled substance.
2006-11-01
A novel LC-ESI-MS-MS method for sensitive quantification of colchicine in human plasma: application to two case reports.
2006-04
A rapid and sensitive high-performance liquid chromatography method for determination of embutramide (a Tanax or T61 component) in human blood with photodiode-array UV detection.
2004-03
Blood investigation in a fatality involving the veterinary drug T-61.
2002-10
Comparison of HPLC and GC-MS methods for determination of embutramide (a component of Tanax or T-61) in biological specimens.
2001-08-14
Patents

Patents

Sample Use Guides

Inject 1 mL of embutramide (in the form of TRIBUTAME Euthanasia Solution) for each 5 pounds body weight (0.45 mL/kg). Administer the calculated dose as a single intravenous bolus injection within a 10- to 15 second period.
Route of Administration: Intravenous
In Vitro Use Guide
Unknown
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:13:58 GMT 2025
Edited
by admin
on Mon Mar 31 18:13:58 GMT 2025
Record UNII
3P4TQG94T1
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
EMBUTRAMID
GREEN BOOK  
Preferred Name English
EMBUTRAMIDE
INN   MART.   USAN  
USAN   INN  
Official Name English
N-(.BETA.,.BETA.-DIETHYL-M-METHOXYPHENETHYL)-4-HYDROXYBUTYRAMIDE
Systematic Name English
embutramide [INN]
Common Name English
EMBUTRAMIDE [USAN]
Common Name English
EMBUTRAMID [GREEN BOOK]
Common Name English
HOE-18-680
Code English
T-61
Code English
EMBUTRAMIDE [MART.]
Common Name English
HOE-18680
Code English
EMBUTANE
Code English
BUTANAMIDE, N-(2-ETHYL-2-(3-METHOXYPHENYL)BUTYL)-4-HYDROXY-
Systematic Name English
HOE 18 680
Code English
Classification Tree Code System Code
DEA NO. 2020
Created by admin on Mon Mar 31 18:13:58 GMT 2025 , Edited by admin on Mon Mar 31 18:13:58 GMT 2025
NCI_THESAURUS C245
Created by admin on Mon Mar 31 18:13:58 GMT 2025 , Edited by admin on Mon Mar 31 18:13:58 GMT 2025
CFR 21 CFR 522.810
Created by admin on Mon Mar 31 18:13:58 GMT 2025 , Edited by admin on Mon Mar 31 18:13:58 GMT 2025
Code System Code Type Description
EVMPD
SUB06502MIG
Created by admin on Mon Mar 31 18:13:58 GMT 2025 , Edited by admin on Mon Mar 31 18:13:58 GMT 2025
PRIMARY
DAILYMED
3P4TQG94T1
Created by admin on Mon Mar 31 18:13:58 GMT 2025 , Edited by admin on Mon Mar 31 18:13:58 GMT 2025
PRIMARY
INN
2160
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PRIMARY
EPA CompTox
DTXSID7057654
Created by admin on Mon Mar 31 18:13:58 GMT 2025 , Edited by admin on Mon Mar 31 18:13:58 GMT 2025
PRIMARY
WIKIPEDIA
EMBUTRAMIDE
Created by admin on Mon Mar 31 18:13:58 GMT 2025 , Edited by admin on Mon Mar 31 18:13:58 GMT 2025
PRIMARY
SMS_ID
100000080774
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PRIMARY
DRUG BANK
DB01487
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PRIMARY
PUBCHEM
27453
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PRIMARY
NCI_THESAURUS
C75093
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PRIMARY
ECHA (EC/EINECS)
239-780-4
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PRIMARY
RXCUI
2464539
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PRIMARY
USAN
GG-100
Created by admin on Mon Mar 31 18:13:58 GMT 2025 , Edited by admin on Mon Mar 31 18:13:58 GMT 2025
PRIMARY
ChEMBL
CHEMBL2104668
Created by admin on Mon Mar 31 18:13:58 GMT 2025 , Edited by admin on Mon Mar 31 18:13:58 GMT 2025
PRIMARY
FDA UNII
3P4TQG94T1
Created by admin on Mon Mar 31 18:13:58 GMT 2025 , Edited by admin on Mon Mar 31 18:13:58 GMT 2025
PRIMARY
CAS
15687-14-6
Created by admin on Mon Mar 31 18:13:58 GMT 2025 , Edited by admin on Mon Mar 31 18:13:58 GMT 2025
PRIMARY
MESH
C059324
Created by admin on Mon Mar 31 18:13:58 GMT 2025 , Edited by admin on Mon Mar 31 18:13:58 GMT 2025
PRIMARY
Related Record Type Details
ACTIVE MOIETY