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Details

Stereochemistry ACHIRAL
Molecular Formula 2C5H9O2.Zn.2H2O
Molecular Weight 303.687
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ZINC VALERATE DIHYDRATE

SMILES

O.O.[Zn++].CCCCC([O-])=O.CCCCC([O-])=O

InChI

InChIKey=RAAZPMAXVMASOJ-UHFFFAOYSA-L
InChI=1S/2C5H10O2.2H2O.Zn/c2*1-2-3-4-5(6)7;;;/h2*2-4H2,1H3,(H,6,7);2*1H2;/q;;;;+2/p-2

HIDE SMILES / InChI

Molecular Formula HO
Molecular Weight 17.0073
Charge -1
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula Zn
Molecular Weight 65.409
Charge 2
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

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

Valeric acid is a colorless, oily liquid with an unpleasant odor. It is highly corrosive and must be handled with care. Valeric acid is mainly used as a chemical intermediate to manufacture flavors and perfumes, synthetic lubricants, agricultural chemicals, and pharmaceuticals. It is also used as a flavoring aid in foods. Valeric acid is considered safe as a food additive by the World Health Organization.

Approval Year

Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Sourcing

Sourcing

Vendor/AggregatorIDURL
PubMed

PubMed

TitleDatePubMed
Evidence for an essential arginine in the flavoprotein nitroalkane oxidase.
2001
The relation of oxidized LDL autoantibodies and long-term hormone replacement therapy to ultrasonographically assessed atherosclerotic plaque quantity and severity in postmenopausal women.
2001 Aug
Selective functionalization of amino acids in water: a synthetic method via catalytic C-H bond activation.
2001 Aug 22
Effect of estradiol valerate alone or in association with cyproterone acetate upon vascular function of postmenopausal women at increased risk for cardiovascular disease.
2001 Dec 14
Effect of the liquid upflow velocity on thermophilic sulphate reduction in acidifying granular sludge reactors.
2001 Feb
Short- and long-term effects of hormone replacement therapy on cardiovascular risk factors in postmenopausal women.
2001 Jul
Biotin reagents for antibody pretargeting. 5. Additional studies of biotin conjugate design to provide biotinidase stability.
2001 Jul-Aug
Intravesical valrubicin in the treatment of carcinoma in situ of the bladder.
2001 Jun
Births after transfer of zona-free blastocysts in oocyte donation cycles.
2001 Mar
Unusual enzymes involved in five pathways of glutamate fermentation.
2001 Oct
Cometabolic biosynthesis of copolyesters consisting of 3-hydroxyvalerate and medium-chain-length 3-hydroxyalkanoates by Pseudomonas sp. DSY-82.
2001 Oct
[High-level production of poly (3-hydroxybutyrate-co-3-hydroxyvalerate) by feb-batch culture of Alcaligenes eutrophus].
2001 Sep
Estradiol valerate/dienogest.
2002
Sensitization of trigeminal caudalis neuronal responses to intraoral acid and salt stimuli and desensitization by nicotine.
2002 Aug
A novel synthesis of (+)-biotin from L-cysteine.
2002 Aug 9
Mesophilic acidification of gelatinaceous wastewater.
2002 Feb 14
Carvacrol and thymol reduce swine waste odor and pathogens: stability of oils.
2002 Jan
Volatile flavor components of stored nonfat dry milk.
2002 Jan 16
Characterization of copolymer hydroxybutyrate/hydroxyvalerate from saponified vernonia, soybean, and "spent" frying oils.
2002 Jul-Aug
1H and (13)C NMR spectroscopic analysis of human saliva.
2002 Jun
A rapid selective extraction procedure for the outer membrane protein (OmpF) from Escherichia coli.
2002 Jun
Structural characterization of in vivo rat glutathione adducts and a hydroxylated metabolite of simvastatin hydroxy acid.
2002 Mar
Evidence for a compound in Comstock-Kellog glands modulating premating behavior in male desert locust, Schistocerca gregaria.
2002 May
Activation of neurons in trigeminal caudalis by noxious oral acidic or salt stimuli is not reduced by amiloride.
2003 Apr 18
Effect of method of application of a fibrolytic enzyme product on digestive processes and milk production in Holstein-Friesian cows.
2003 Feb
Dynamics of the anaerobic process: effects of volatile fatty acids.
2003 Jun 30
Improvement of (+)-catechin inhibitory activity on human PMN respiratory burst by (+)-3-O-propionyl and (-)-3-O-valeryl substitution.
2003 Mar
Lack of quinine-evoked activity in rat trigeminal subnucleus caudalis.
2003 Mar
Optimizing the level of wet corn gluten feed in the diet of lactating dairy cows.
2003 Mar
Left ventricular diastolic function assessment by tissue Doppler echocardiography in relation to hormonal replacement therapy in postmenopausal women with diastolic dysfunction.
2003 Mar-Apr
Synthesis, X-ray crystal structure, UV/visible linear and nonlinear (optical limiting) spectral properties of symmetrical and unsymmetrical porphyrazines with annulated 1,2,5-thiadiazole and 1,4-diamyloxybenzene moieties.
2003 Sep 5
The degradability of biodegradable plastics in aerobic and anaerobic waste landfill model reactors.
2004 Jan
Short-chain fatty acids stimulate leptin production in adipocytes through the G protein-coupled receptor GPR41.
2004 Jan 27
Sequential feeding of glucose and valerate in a fed-batch culture of Ralstonia eutropha for production of poly(hydroxybutyrate-co-hydroxyvalerate) with high 3-hydroxyvalerate fraction.
2004 Jan-Feb
Patents

Sample Use Guides

In Vivo Use Guide
Unknown
Route of Administration: Unknown
1.5 mM valeric acid is an effective chemical reagent to increase mAb production in rCHO cells.
Substance Class Chemical
Created
by admin
on Fri Dec 15 17:22:57 GMT 2023
Edited
by admin
on Fri Dec 15 17:22:57 GMT 2023
Record UNII
MN0RX54EQA
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
ZINC VALERATE DIHYDRATE
WHO-DD  
Systematic Name English
PENTANOIC ACID, ZINC SALT, DIHYDRATE
Common Name English
ZINCUM VALERIANICUM
HPUS  
Common Name English
Zinc valerate dihydrate [WHO-DD]
Common Name English
PENTANOIC ACID, ZINC SALT, HYDRATE (2:1:2)
Common Name English
ZINC VALERATE, DIHYDRATE
Systematic Name English
ZINCUM VALERIANICUM [HPUS]
Common Name English
Code System Code Type Description
DAILYMED
MN0RX54EQA
Created by admin on Fri Dec 15 17:22:57 GMT 2023 , Edited by admin on Fri Dec 15 17:22:57 GMT 2023
PRIMARY
SMS_ID
100000128288
Created by admin on Fri Dec 15 17:22:57 GMT 2023 , Edited by admin on Fri Dec 15 17:22:57 GMT 2023
PRIMARY
PUBCHEM
71586833
Created by admin on Fri Dec 15 17:22:57 GMT 2023 , Edited by admin on Fri Dec 15 17:22:57 GMT 2023
PRIMARY
EVMPD
SUB35131
Created by admin on Fri Dec 15 17:22:57 GMT 2023 , Edited by admin on Fri Dec 15 17:22:57 GMT 2023
PRIMARY
EVMPD
SUB129980
Created by admin on Fri Dec 15 17:22:57 GMT 2023 , Edited by admin on Fri Dec 15 17:22:57 GMT 2023
PRIMARY
CAS
5970-56-9
Created by admin on Fri Dec 15 17:22:57 GMT 2023 , Edited by admin on Fri Dec 15 17:22:57 GMT 2023
PRIMARY
EPA CompTox
DTXSID70208415
Created by admin on Fri Dec 15 17:22:57 GMT 2023 , Edited by admin on Fri Dec 15 17:22:57 GMT 2023
PRIMARY
FDA UNII
MN0RX54EQA
Created by admin on Fri Dec 15 17:22:57 GMT 2023 , Edited by admin on Fri Dec 15 17:22:57 GMT 2023
PRIMARY
RXCUI
1309408
Created by admin on Fri Dec 15 17:22:57 GMT 2023 , Edited by admin on Fri Dec 15 17:22:57 GMT 2023
PRIMARY RxNorm
Related Record Type Details
PARENT -> SALT/SOLVATE
PARENT -> SALT/SOLVATE
ANHYDROUS->SOLVATE
Related Record Type Details
ACTIVE MOIETY