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Key Documents

47190

Sigma-Aldrich

5-Fluoroorotic acid hydrate

≥99.0% (TLC)

Synonym(s):

2,6-Dihydroxy-5-fluoropyrimidine-4-carboxylic acid, 5-Fluorouracil-4-carboxylic acid

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About This Item

Empirical Formula (Hill Notation):
C5H3FN2O4 · xH2O
CAS Number:
Molecular Weight:
174.09 (anhydrous basis)
EC Number:
MDL number:
UNSPSC Code:
12352204
PubChem Substance ID:
NACRES:
NA.25

Quality Level

assay

≥99.0% (TLC)

form

solid

mp

278 °C (dec.) (lit.)

solubility

4 M NH4OH: 50 mg/mL, clear, faintly yellow

storage temp.

−20°C

SMILES string

OC(C(NC(N1)=O)=C(F)C1=O)=O.[H]O[H]

InChI

1S/C5H3FN2O4.H2O/c6-1-2(4(10)11)7-5(12)8-3(1)9;/h(H,10,11)(H2,7,8,9,12);1H2

InChI key

LODRRYMGPWQCTR-UHFFFAOYSA-N

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Application

Useful in the selection of orotidine-5′-phosphate decarboxylase mutants of Saccharomyces cerevisiae.

Other Notes

Selective agent in yeast molecular genetics

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


Certificates of Analysis (COA)

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J D Boeke et al.
Methods in enzymology, 154, 164-175 (1987-01-01)
5-FOA is an extremely useful reagent for the selection of Ura- cells amid a population of Ura+ cells. The selection is effective in transformation and recombination studies where loss of URA3+ is desired. A new plasmid shuffling procedure based on

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