C.I.Acid yellow 3
CAS: 8004-92-0
Rif. 3D-FA41315
10g | Fuori produzione | ||
25g | Fuori produzione | ||
50g | Fuori produzione | ||
100g | Fuori produzione | ||
250g | Fuori produzione |
Informazioni sul prodotto
- 1,3-Isobenzofurandione, reaction products with methylquinoline and quinoline, sulfonated
- Acid Quinoline Yellow Ws
- Acid Yellow QS
- Anhydride phtalique, produits de reaction avec la methylquinoline et la quinoline sulfurises
- Basacid Yellow 094
- Basovit Yellow 095E
- Cogilor Yellow 112.12
- D & C Yellow 10
- D and C Yellow No. 10
- D&C Yellow No. 10
- Vedi altri sinonimi
- D&C Yellow No. 10-307007
- D&C Yellow No. 10-38009
- D&C Yellow No. 10-38012
- D&C Yellow No. 10-90125
- D&C Yellow No. 10HWS307010
- D&C Yellow No. 10W074
- Dye Quinoline Yellow
- E 104
- E 104 (dye)
- Eurocert Quinoline Yellow 311744
- FD and C Yellow No. 10
- FD&C Yellow No. 10
- Food Yellow No. 13
- Japan Yellow 203
- Lemon Yellow ZN 3
- Neelicol Quinoline Yellow WS
- Puricolor Yellow FYE 13
- Quinidine Yellow KT
- Quinoline Yellow
- Quinoline Yellow 36012
- Quinoline Yellow 38009
- Quinoline Yellow 90125
- Quinoline Yellow 90145
- Quinoline Yellow Certifiable 307006
- Quinoline Yellow E 104
- Quinoline Yellow Extra
- Quinoline Yellow Lake
- Quinoline Yellow S
- Quinoline Yellow WG-G
- Quinoline Yellow WG-G Conc
- Quinoline Yellow WS
- Quinolone Yellow Extra
- Vitasyn Quinoline Yellow 70
- Yellow 10
- Yellow No. 10
- Yellow No. 203
- disodium 2-(1,3-dioxo-2,3-dihydro-1H-inden-2-yl)quinoline-6,8-disulfonate
- C.I. 47005
- C.I. Acid Yellow 3
- C.I. Acid Yellow 3
- C.I. Food Yellow 13
C.I.Acid yellow 3 is a fluorescent dye that belongs to the class of trifluoroacetic acid dyes. It is soluble in water, slightly soluble in ethanol, and insoluble in acetone and ether. C.I.Acid yellow 3 has been shown to be genotoxic in human serum, as well as being able to bind to DNA through electrostatic interactions with phosphate groups on the backbone of DNA or on the surface of negatively charged DNA phosphate groups. The dye has also been shown to inhibit polymerase chain reactions (PCRs) by binding to the primers during amplification of DNA and increasing the rate of primer-dimers formation, thereby preventing synthesis of new strands of DNA from occurring.