F7876

Folic acid

≥97%

• Sinónimos: PteGlu, Pteroyl-L-glutamic acid, Vitamin M
• Fórmula empírica (notación de Hill): C₁₉H₁₉N₇O₆
• Número de CAS: 59-30-3
• Peso molecular: 441.40
• Beilstein: 100781
• Número CE: 200-419-0
• Número MDL: MFCD00079305
• Código UNSPSC: 12352106
• eCl@ss: 34058014
• ID de la sustancia en PubChem: 57654192
• NACRES: NA.79

Propiedades

• origen biológico: synthetic (organic)
• Ensayo: ≥97%
• Formulario: powder
• técnicas: HPLC: suitable
• color: faint orange to dark orange-yellow; faint yellow to dark yellow
• mp: >285 °C
• temp. de almacenamiento: room temp
• cadena SMILES: NC(N1)=NC(C2=C1N=CC(CNC3=CC=C(C(N[C@@H](CCC(O)=O)C(O)=O)=O)C=C3)=N2)=O
• InChI: 1S/C19H19N7O6/c20-19-25-15-14(17(30)26-19)23-11(8-22-15)7-21-10-3-1-9(2-4-10)16(29)24-12(18(31)32)5-6-13(27)28/h1-4,8,12,21H,5-7H2,(H,24,29)(H,27,28)(H,31,32)(H3,20,22,25,26,30)/t12-/m0/s1
• Clave InChI: OVBPIULPVIDEAO-LBPRGKRZSA-N

Descripción

Aplicación

Folic acid has been used:

• to induce acute kidney injury in mice
• as a supplement to cultivate MCF-7 breast cancer cells.
• to construct folate or TNF-related apoptosis-including ligand (TRAIL)-conjugated nanomicelles

Acciones bioquímicas o fisiológicas

Enzyme cofactor essential for the synthesis, methylation, and repair of DNA. Folic acid supplements may reduce colorectal cancer risk.

Folic acid (FA) and dihydrofolic acid (FAH2) are substrates of dihydrofolate reductase(s) which reduce them to tetrahydrofolate (THF), which in turn supports ‘one carbon′ transfer. Tetrahydrofolates are required for de novo synthesis of purines, thymidylic acid and various amino acids and for post-translational methylation (epigenetics).

Información de seguridad

• Código de clase de almacenamiento: 11 - Combustible Solids
• Clase de riesgo para el agua (WGK): WGK 1
• Punto de inflamabilidad (°F): Not applicable
• Punto de inflamabilidad (°C): Not applicable
• Equipo de protección personal: Eyeshields, Gloves, type N95 (US)