Orotic acid - >98.0%, high purity , CAS No.65-86-1

1 Citations
Item Number
O137322
Grouped product items
SKUSizeAvailabilityPrice Qty
O137322-25g
25g
In stock
$28.90
O137322-100g
100g
In stock
$86.90
O137322-500g
500g
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$232.90

Intermediate in pyrimidine metabolism

Basic Description

SynonymsOrotic acid | 65-86-1 | 6-Carboxyuracil | Oropur | Orodin | Orotonin | Orotyl | Orotonsan | Vitamin B13 | Whey factor | Oroturic | 2,6-dioxo-1,2,3,6-tetrahydropyrimidine-4-carboxylic acid | Uracil-6-carboxylic acid | Animal galactose factor | 6-Uracilcarboxylic acid | Molkensaeure | Oro
Specifications & PurityMoligand™, ≥98%
Biochemical and Physiological MechanismsIntermediate in pyrimidine metabolism. Increases hepatic triacylglycerol levels in vivo . Cardioprotective.
Shipped InNormal
GradeMoligand™
NoteWherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.
Product Description

Orotic acid is a heterocyclic compound and an acid. It was once believed to be part of the vitamin B complex and was called vitamin B13, but it is now known that it is not a vitamin but is instead manufactured in the body by intestinal flora. Its salts, known as orotates, are sometimes used as mineral carriers in some dietary supplements, to increase their bioavailability. It is an intermediate in de novo pyrimidine biosynthesis that may be used to study the specificity and kinetics of orotate phosphoribosyltransferase (OPRT) which catalyzes the reversible phosphoribosyl transfer from 5′-phospho-α-d-ribose 1′-diphosphate (PRPP) to orotic acid, forming pyrophosphate and orotidine 5′-monophosphate (OMP). It may be used to study dependent cell signaling pathways and transcription regulation mechanisms that induce hepatic lipogenesis.
An intermediate in de novo pyrimidine biosynthesis.

Associated Targets(Human)

DHODH Tclin Dihydroorotate dehydrogenase (quinone), mitochondrial (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
SLC2A9 Tbio Solute carrier family 2, facilitated glucose transporter member 9 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
HDAC6 Tclin Histone deacetylase 6 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
LMNA Tbio Prelamin-A/C (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
ALDH1A1 Tchem Retinal dehydrogenase 1 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
PPARG Tclin Peroxisome proliferator-activated receptor gamma (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
PPARG Tclin Peroxisome proliferator-activated receptor gamma (15191 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ALDH1A1 Tchem Aldehyde dehydrogenase 1A1 (77053 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
LMNA Tbio Prelamin-A/C (36751 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLC2A9 Tbio Solute carrier family 2, facilitated glucose transporter member 9 (15 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Hdac6 Histone deacetylase 6 (222 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Plasmodium falciparum (966862 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
rep Replicase polyprotein 1ab (378 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ffp 4'-phosphopantetheinyl transferase ffp (24982 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
DHODH Dihydroorotate dehydrogenase (fumarate) (195 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SARS-CoV-2 (38078 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Names and Identifiers

Pubchem Sid488179577
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488179577
IUPAC Name 2,4-dioxo-1H-pyrimidine-6-carboxylic acid
INCHI InChI=1S/C5H4N2O4/c8-3-1-2(4(9)10)6-5(11)7-3/h1H,(H,9,10)(H2,6,7,8,11)
InChi Key PXQPEWDEAKTCGB-UHFFFAOYSA-N
Canonical SMILES C1=C(NC(=O)NC1=O)C(=O)O
Isomeric SMILES C1=C(NC(=O)NC1=O)C(=O)O
WGK Germany 3
RTECS RM3180000
PubChem CID 967
Molecular Weight 156.1
Beilstein 383901

Certificates

Certificate of Analysis(COA)

Enter Lot Number to search for COA:

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10 results found

Lot NumberCertificate TypeDateItem
G2219769Certificate of AnalysisMay 15, 2024 O137322
G2219770Certificate of AnalysisMay 15, 2024 O137322
G2219771Certificate of AnalysisMay 15, 2024 O137322
G2219772Certificate of AnalysisMay 15, 2024 O137322
C2110011Certificate of AnalysisDec 14, 2022 O137322
C2110012Certificate of AnalysisDec 14, 2022 O137322
K2217186Certificate of AnalysisNov 23, 2022 O137322
A2423104Certificate of AnalysisMar 30, 2022 O137322
K2216310Certificate of AnalysisMar 30, 2022 O137322
C2204053Certificate of AnalysisMar 14, 2022 O137322

Chemical and Physical Properties

SolubilitySoluble in Sodium Hydroxide

Safety and Hazards(GHS)

Pictogram(s) GHS07
Signal Warning
Hazard Statements

H315:Causes skin irritation

H319:Causes serious eye irritation

H335:May cause respiratory irritation

Precautionary Statements

P261:Avoid breathing dust/fume/gas/mist/vapors/spray.

P305+P351+P338:IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses if present and easy to do - continue rinsing.

P280:Wear protective gloves/protective clothing/eye protection/face protection.

P302+P352:IF ON SKIN: wash with plenty of water.

P321:Specific treatment (see ... on this label).

P405:Store locked up.

P501:Dispose of contents/container to ...

P264:Wash hands [and …] thoroughly after handling.

P271:Use only outdoors or in a well-ventilated area.

P304+P340:IF INHALED: Remove person to fresh air and keep comfortable for breathing.

P403+P233:Store in a well-ventilated place. Keep container tightly closed.

P362+P364:Take off contaminated clothing and wash it before reuse.

P264+P265:Wash hands [and …] thoroughly after handling. Do not touch eyes.

P337+P317:If eye irritation persists: Get medical help.

P332+P317:If skin irritation occurs: Get medical help.

P319:Get medical help if you feel unwell.

WGK Germany 3
RTECS RM3180000

Related Documents

Citations of This Product

1. Yongyan Yang, Gangying Feng, Jingfei Wang, Ruiting Zhang, Shuangling Zhong, Jia Wang, Xuejun Cui.  (2023)  Injectable chitosan-based self-healing supramolecular hydrogels with temperature and pH dual-responsivenesses.  INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES,  227  (1038).  [PMID:36460241]

References

1. Yongyan Yang, Gangying Feng, Jingfei Wang, Ruiting Zhang, Shuangling Zhong, Jia Wang, Xuejun Cui.  (2023)  Injectable chitosan-based self-healing supramolecular hydrogels with temperature and pH dual-responsivenesses.  INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES,  227  (1038).  [PMID:36460241]

Solution Calculators