O2750

Orotic acid

≥98% (titration), anhydrous

• Synonyme(s) : 2,6-Dihydroxypyrimidine-4-carboxylic acid, 6-Carboxy-2,4-dihydroxypyrimidine, 6-Carboxyuracil, Uracil-6-carboxylic acid
• Formule empirique (notation de Hill) : C₅H₄N₂O₄
• Numéro CAS: 65-86-1
• Poids moléculaire : 156.10
• UNSPSC Code: 41106305
• NACRES: NA.51
• PubChem Substance ID: 24897967
• EC Number: 200-619-8
• Beilstein/REAXYS Number: 383901
• MDL number: MFCD00006027
• Assay: ≥98% (titration)

Propriétés

• grade: anhydrous
• Quality Segment: 200
• assay: ≥98% (titration)
• mp: ≥300 °C
• SMILES string: OC(=O)C1=CC(=O)NC(=O)N1
• 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

Description

Application

Orotic acid (OA) 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 (OA), forming pyrophosphate and orotidine 5′-monophosphate (OMP). Orotic acid is used as a starting material for the potential commercial bioproduction of uridine 5′-monophosphate (UMP) by microbes such as Corynebacterium ammoniagenes (ATCC 6872) or Saccharomyces cerevisiae. OA may be used to study the AMPK/SREBP-1 dependent cell signaling pathway and transcription regulation mechanisms that induce hepatic lipogenesis.

Informations sur la sécurité

• pictograms: GHS07
• signalword: Warning
• hcodes: H302,H315,H319,H335
• pcodes: P261 - P264 - P271 - P301 + P312 - P302 + P352 - P305 + P351 + P338
• Hazard Classifications: Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
• target_organs: Respiratory system
• Classe de stockage: 11 - Combustible Solids
• wgk: WGK 3
• flash_point_f: Not applicable
• flash_point_c: Not applicable
• ppe: dust mask type N95 (US), Eyeshields, Gloves