| Identification | More | [Name]
Sulfobromophthalein sodium | [CAS]
123359-42-2 | [Synonyms]
3,3'-(4,5,6,7-tetrabromo-3-oxo-1(3h)-isobenzofuranylidene)bis(6-hydroxy-benzenesulfonic acid) disodium salt
BROMOSULFALEIN
bromosulfalein sodium
BROMOSULFONPHTHALEIN
BROMOSULFOPHTHALEIN
BROMOSULFOPHTHALEIN SODIUM SALT
BROMO SULPHALEIN
BROMOSULPHALEIN DISODIUM SALT
PHENOLTETRABROMOPHTHALEIN-3',3''-DISULFONIC ACID DISODIUM SALT
SODIUM SULFOBROMOPHTHALEIN
SULFOBROMOPHTHALEIN
SULFOBROMOPHTHALEIN DISODIUM SALT
sulfobromophthalein sodium
SULFOBROMOPHTHALEIN SODIUM SALT
bromsulfalein sodium
SULFORBROMOPHTHALEINSODIUMHYDRATE
3,3'-(4,5,6,7-Tetrabromo-3-oxo-1(3H)-isobenzofuranylidene)bis(6-hydroxy-benzenesulfonic acid) disodium salt
Sulfobromophthalein hydrate sodium salt | [EINECS(EC#)]
200-761-0 | [Molecular Formula]
C20H8Br4Na2O10S2 | [MDL Number]
MFCD00012442 | [Molecular Weight]
838 | [MOL File]
123359-42-2.mol |
| Safety Data | Back Directory | [Hazard Codes ]
Xn | [Risk Statements ]
R42/43:May cause sensitization by inhalation and skin contact . | [Safety Statements ]
S22:Do not breathe dust .
S36/37:Wear suitable protective clothing and gloves .
S45:In case of accident or if you feel unwell, seek medical advice immediately (show label where possible) . | [WGK Germany ]
3
| [RTECS ]
SM8395000
| [HS Code ]
29329900 |
| Hazard Information | Back Directory | [Description]
A blue dye used in the assessment of
hepatobiliary dysfunction. The concentration in plasma is
monitored since dye removal from the blood is delayed in
hepatic dysfunction. Experimentally the appearance of sulfobromphthalein in the bile can also be measured. | [Chemical Properties]
White, crystalline powder; odorless; bit-
ter taste. Hygroscopic; soluble in water; insoluble
in alcohol and acetone.
| [Biochem/physiol Actions]
Sulfobromophthalein (BSP) is a high affinity organic ion substrate for organic anion transporting polypeptides (OATPs) and has been used as a substrate for multidrug resistance associated protein 2 (Mrp2). BSP is transported into hepatocytes by OATPs and, after conjugation to glutathione, is excreted into bile by Mrp2. It was found to inhibit the aldo-keto reductase ARK1C20. |
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Sigma-Aldrich
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https://www.sigmaaldrich.cn |
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