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Details

Stereochemistry ACHIRAL
Molecular Formula C6H5O7.H.2H4N
Molecular Weight 226.1846
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of AMMONIUM CITRATE, DIBASIC

SMILES

[H+].[NH4+].[NH4+].OC(CC([O-])=O)(CC([O-])=O)C([O-])=O

InChI

InChIKey=YXVFQADLFFNVDS-UHFFFAOYSA-N
InChI=1S/C6H8O7.2H3N/c7-3(8)1-6(13,5(11)12)2-4(9)10;;/h13H,1-2H2,(H,7,8)(H,9,10)(H,11,12);2*1H3

HIDE SMILES / InChI

Molecular Formula H4N
Molecular Weight 18.0385
Charge 1
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula C6H5O7
Molecular Weight 189.0997
Charge -3
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula H
Molecular Weight 1.0079
Charge 1
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 http://www.adm.com/en-US/worldwide/australia/Documents/Potassium%20Citrate%20AU.pdf | https://noshly.com/additive/e332/acidity-regulator-plus/332/#.WUp-1uvyjIU

Potassium citrate is indicated for the management of renal tubular acidosis with calcium stones, hypocitraturic calcium oxalate nephrolithiasis of any etiology, uric acid lithiasis with or without calcium stones. WhenPotassium citrate is given orally, the metabolism of absorbed citrate produces an alkaline load. The induced alkaline load in turn increases urinary pH and raises urinary citrate by augmenting citrate clearance without measurably altering ultrafilterable serum citrate. Thus, potassium citrate therapy appears to increase urinary citrate principally by modifying the renal handling of citrate, rather than by increasing the filtered load of citrate. Potassium citrate is used as a food additive (E 332) to regulate acidity.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
UROCIT-K

Approved Use

Urocit®-K is a citrate salt of potassium indicated for the management of: • Renal tubular acidosis (RTA) with calcium stones • Hypocitraturic calcium oxalate nephrolithiasis of any etiology • Uric acid lithiasis with or without calcium stones

Launch Date

4.94121615E11
Primary
UROCIT-K

Approved Use

Urocit®-K is a citrate salt of potassium indicated for the management of: • Renal tubular acidosis (RTA) with calcium stones • Hypocitraturic calcium oxalate nephrolithiasis of any etiology • Uric acid lithiasis with or without calcium stones

Launch Date

4.94121615E11
Doses

Doses

DosePopulationAdverse events​
540 mg 1 times / day multiple, oral
Recommended
Dose: 540 mg, 1 times / day
Route: oral
Route: multiple
Dose: 540 mg, 1 times / day
Co-administed with::
Thiamin oral 1.1 mg
Arginine oral 1240 mg
caffeine oral 52 mg
Sources: Page: p.2326
healthy, 24-59
n = 16
Health Status: healthy
Age Group: 24-59
Sex: M+F
Population Size: 16
Sources: Page: p.2326
Sourcing

Sourcing

Vendor/AggregatorIDURL
PubMed

PubMed

TitleDatePubMed
Comparative efficacy of "specific" potassium citrate therapy versus conservative management in nephrolithiasis of mild to moderate severity.
1985 Oct
Patents

Sample Use Guides

In Vivo Use Guide
Objective: To restore normal urinary citrate (greater than 320 mg/day and as close to the normal mean of 640 mg/day as possible), and to increase urinary pH to a level of 6.0 to 7.0. • Severe hypocitraturia (urinary citrate < 150 mg/day): therapy should be initiated at 60 mEq per day; a dose of 30 mEq two times per day or 20 mEq three times per day with meals or within 30 minutes after meals or bedtime snack • Mild to moderate hypocitraturia (urinary citrate >150 mg/day): therapy should be initiated at 30 mEq per day; a dose of 15 mEq two times per day or 10 mEq three times per day with meals or within 30 minutes after meals or bedtime snack
Route of Administration: Oral
In Vitro Use Guide
Unknown
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:20:23 UTC 2023
Edited
by admin
on Fri Dec 15 15:20:23 UTC 2023
Record UNII
N9BUG430K8
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
AMMONIUM CITRATE, DIBASIC
FCC   MI  
Common Name English
2-HYDROXY-1,2,3-PROPANETRICARBOXYLIC ACID AMMONIUM SALT (1:2)
Common Name English
DIAMMONIUM CITRATE [INCI]
Common Name English
DIAMMONIUM HYDROGEN CITRATE
Systematic Name English
AMMONIUM CITRATE, DIBASIC [FCC]
Common Name English
AMMONIUM CITRICUM
HPUS  
Common Name English
DIAMMONIUM CITRATE [HSDB]
Common Name English
DIAMMONIUM HYDROGEN 2-HYDROXYPROPANE-1,2,3-TRICARBOXYLATE
Systematic Name English
AMMONIUM CITRATE, DIBASIC [MI]
Common Name English
1,2,3-PROPANETRICARBOXYLIC ACID, 2-HYDROXY-, DIAMMONIUM SALT
Common Name English
DIAMMONIUM CITRATE
HSDB   INCI  
INCI  
Official Name English
AMMONIUM CITRICUM [HPUS]
Common Name English
Classification Tree Code System Code
CFR 21 CFR 184.1140
Created by admin on Fri Dec 15 15:20:23 UTC 2023 , Edited by admin on Fri Dec 15 15:20:23 UTC 2023
Code System Code Type Description
CHEBI
63076
Created by admin on Fri Dec 15 15:20:23 UTC 2023 , Edited by admin on Fri Dec 15 15:20:23 UTC 2023
PRIMARY
MERCK INDEX
m1779
Created by admin on Fri Dec 15 15:20:23 UTC 2023 , Edited by admin on Fri Dec 15 15:20:23 UTC 2023
PRIMARY Merck Index
EPA CompTox
DTXSID5020079
Created by admin on Fri Dec 15 15:20:23 UTC 2023 , Edited by admin on Fri Dec 15 15:20:23 UTC 2023
PRIMARY
ECHA (EC/EINECS)
221-146-3
Created by admin on Fri Dec 15 15:20:23 UTC 2023 , Edited by admin on Fri Dec 15 15:20:23 UTC 2023
PRIMARY
CAS
3012-65-5
Created by admin on Fri Dec 15 15:20:23 UTC 2023 , Edited by admin on Fri Dec 15 15:20:23 UTC 2023
PRIMARY
SMS_ID
100000131771
Created by admin on Fri Dec 15 15:20:23 UTC 2023 , Edited by admin on Fri Dec 15 15:20:23 UTC 2023
PRIMARY
PUBCHEM
18171
Created by admin on Fri Dec 15 15:20:23 UTC 2023 , Edited by admin on Fri Dec 15 15:20:23 UTC 2023
PRIMARY
HSDB
300
Created by admin on Fri Dec 15 15:20:23 UTC 2023 , Edited by admin on Fri Dec 15 15:20:23 UTC 2023
PRIMARY
FDA UNII
N9BUG430K8
Created by admin on Fri Dec 15 15:20:23 UTC 2023 , Edited by admin on Fri Dec 15 15:20:23 UTC 2023
PRIMARY
EVMPD
SUB46258
Created by admin on Fri Dec 15 15:20:23 UTC 2023 , Edited by admin on Fri Dec 15 15:20:23 UTC 2023
PRIMARY
Related Record Type Details
PARENT -> SALT/SOLVATE