ChemicalBook--->CAS DataBase List--->150408-83-6

150408-83-6

150408-83-6 Structure

150408-83-6 Structure
IdentificationBack Directory
[Name]

5(6)-Carboxytetramethylrhodamine succinimidyl ester
[CAS]

150408-83-6
[Synonyms]

NHS-RHODAMINE
5(6)-CarboxytetraMet
NHS-5(6)Carboxyrhodamine
NHS-5(6)Carboxyrhodamine (Mixture of 2 Isomers)
5,6-CARBOXYTETRAMETHYLRHODAMINE, SUCCINIMIDE ESTER
5(6)-Carboxytetramethylrhodamine succinimidyl ester
5-CARBOXYTETRAMETHYLRHODAMINE N-HYDROXYSUCCINIMIDE ESTER
5-(AND-6)-CARBOXYTETRAMETHYLRHODAMINE, SUCCINIMIDYL ESTER
5(6)-CARBOXYTETRAMETHYL-RHODAMINE N-HYDROXY-SUCCINIMIDE ESTER
5(6)-TAMRA, SE [5(6)-CarboxytetraMethylrhodaMine, succiniMidyl ester]
9-[2-Carboxy-4(or 5)-[[(2,5-dioxo-1-pyrrolidinyl)oxy]carbonyl]phenyl]-3,6-bis(dimethylamino)-xanthylium inner salt
2,5-Pyrrolidinedione, 1-[[[3',6'-bis(diMethylaMino)-3-oxospiro[isobenzofuran-1(3H),9'-[9H]xan then]-5(or 6)-yl]carbonyl]oxy]-
2,5-Pyrrolidinedione,1-[[[3',6'-bis(dimethylamino)-3-oxospiro[isobenzofuran-1(3H),9'-[9H]xanthen]-5(or6)-yl]carbonyl]oxy]- (9CI)
[Molecular Formula]

C29H25N3O7
[MDL Number]

MFCD00077324
[MOL File]

150408-83-6.mol
[Molecular Weight]

527.52
Chemical PropertiesBack Directory
[storage temp. ]

−20°C
[solubility ]

DMF: soluble
[form ]

powder
[Appearance]

Purple solid
[ex/em]

550/576 nm (MeOH/PBS)
[ε(extinction coefficient)]

90000 L⋅mol−1⋅cm−1
[Φ(quantum yield)]

0.1
[BRN ]

8739319
[InChIKey]

CXYYHBMOVJJZTD-UHFFFAOYSA-N
[SMILES]

CN(C)c1ccc2c(Oc3cc(ccc3C24OC(=O)c5cc(ccc45)C(=O)ON6C(=O)CCC6=O)N(C)C)c1
Safety DataBack Directory
[WGK Germany ]

3
[F ]

8-10-21
[Storage Class]

11 - Combustible Solids
Hazard InformationBack Directory
[Chemical Properties]

Appearance: Purple solid
ex/em: 550/576 nm (MeOH/PBS)
Extinction coefficient (ε): 90000 L??mol??1??cm??1
Quantum yield (Φ): 0.1
[Uses]

 Amine-reactive fluorescent probe for proteins and peptides conjugation
[Uses]

5(6)-Carboxytetramethylrhodamine succinimidyl ester is one of the most commonly used red fluorescent dyes. The succinimidyl ester reacts readily with primary or secondary amines under mild conditions.
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