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Details

Stereochemistry ACHIRAL
Molecular Formula C5H10O2
Molecular Weight 102.1317
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ETHYL PROPIONATE

SMILES

CCOC(=O)CC

InChI

InChIKey=FKRCODPIKNYEAC-UHFFFAOYSA-N
InChI=1S/C5H10O2/c1-3-5(6)7-4-2/h3-4H2,1-2H3

HIDE SMILES / InChI

Molecular Formula C5H10O2
Molecular Weight 102.1317
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Ethyl propionate causes topical dissolution of cholesterol gallbladder. It was tested on an animal model of gallstones in 1997, however, there is no information about its further development.

Approval Year

Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Unknown

Approved Use

Unknown
PubMed

PubMed

TitleDatePubMed
Acute effects of topical methyl tert-butyl ether or ethyl propionate on gallbladder histology in animals: a comparison of two solvents for contact dissolution of cholesterol gallstones.
1992 Oct
Addition of dimethylsulphoxide to methyl-tert-butyl ether and ethyl propionate increases cholesterol dissolving capacity and cholesterol gall stone dissolution in vitro.
1994 Nov
Ethyl propionate is more effective and less cytotoxic than methyl tert-butyl ether for topical gallstone dissolution.
1997 Jul
Local and systemic effects of intraduodenal exposure to topical gallstone solvents ethyl propionate and methyl tert-butyl ether in the rabbit.
1997 Mar

Sample Use Guides

In a preclinical study, ethyl propionate was infused intraduodenally for 3 hr in 32 male New Zealand rabbits.
Route of Administration: Other
In Vitro Use Guide
Human cholesterol gallstones were put in separate glass test tubes, hepatic bile (2 ml) was added and gallstones were subsequently dissolved in 8 ml of either ethyl propionate or ethyl propionate/dimethyl sulphoxide (70/30). The in vivo situation was mimicked by creating turbulence manually using glass syringes (4-6 cycles a minute) and by exchanging solvents and bile every 15 minutes. Test tubes were incubated in the dark at 37 degrees Celsius. No cholesterol stone dissolved completely within the frame of 300 minutes, leaving a mean stone residue of 35% in ethyl propionate and 28% ethyl propionate/dimethyl sulphoxide mixture.
Substance Class Chemical
Created
by admin
on Sat Dec 16 05:11:59 GMT 2023
Edited
by admin
on Sat Dec 16 05:11:59 GMT 2023
Record UNII
AT9K8FY49U
Record Status Validated (UNII)
Record Version
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Name Type Language
ETHYL PROPIONATE
FCC   FHFI   MI  
Systematic Name English
ETHYL PROPIONATE [FHFI]
Common Name English
ETHYL PROPIONATE [MI]
Common Name English
NSC-8848
Code English
PROPIONIC ESTER
Common Name English
ETHYL PROPIONATE [FCC]
Common Name English
PROPANOIC ACID ETHYL ESTER
Systematic Name English
PROPIONIC ACID, ETHYL ESTER
Common Name English
PROPIONIC ETHER
Common Name English
FEMA NO. 2456
Code English
Classification Tree Code System Code
JECFA EVALUATION ETHYL PROPIONATE
Created by admin on Sat Dec 16 05:11:59 GMT 2023 , Edited by admin on Sat Dec 16 05:11:59 GMT 2023
CFR 21 CFR 172.515
Created by admin on Sat Dec 16 05:11:59 GMT 2023 , Edited by admin on Sat Dec 16 05:11:59 GMT 2023
Code System Code Type Description
ECHA (EC/EINECS)
203-291-4
Created by admin on Sat Dec 16 05:11:59 GMT 2023 , Edited by admin on Sat Dec 16 05:11:59 GMT 2023
PRIMARY
JECFA MONOGRAPH
313
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PRIMARY
CAS
105-37-3
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EPA CompTox
DTXSID1040110
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PRIMARY
MERCK INDEX
m5169
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PRIMARY Merck Index
MESH
C069373
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PRIMARY
HSDB
5366
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EVMPD
SUB126387
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WIKIPEDIA
ETHYL PROPIONATE
Created by admin on Sat Dec 16 05:11:59 GMT 2023 , Edited by admin on Sat Dec 16 05:11:59 GMT 2023
PRIMARY
NSC
8848
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PRIMARY
FDA UNII
AT9K8FY49U
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PRIMARY
PUBCHEM
7749
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PRIMARY
SMS_ID
100000151948
Created by admin on Sat Dec 16 05:11:59 GMT 2023 , Edited by admin on Sat Dec 16 05:11:59 GMT 2023
PRIMARY