21955

5(6)-Carboxytetramethylrhodamine N-succinimidyl ester

BioReagent, suitable for fluorescence, ≥70% (coupling to amines)

• Formule empirique (notation de Hill) : C₂₉H₂₅N₃O₇
• Numéro CAS: 150408-83-6
• Poids moléculaire : 527.52
• UNSPSC Code: 12352116
• NACRES: NA.32
• PubChem Substance ID: 57647956
• MDL number: MFCD00077324
• Beilstein/REAXYS Number: 8739319

Propriétés

• product line: BioReagent
• Quality Segment: 100
• assay: ≥70% (coupling to amines)
• form: powder
• solubility: DMF: soluble, acetonitrile: soluble, methanol: soluble
• fluorescence: λ_ex 543 nm; λ_em 576 nm in methanol, λ_ex 554 nm; λ_em 584 nm in 0.1 M phosphate pH 8.0
• suitability: suitable for fluorescence
• storage temp.: −20°C
• SMILES string: CN(C)c1ccc2c(Oc3cc(ccc3C24OC(=O)c5cc(ccc45)C(=O)ON6C(=O)CCC6=O)N(C)C)c1
• InChI: 1S/C29H25N3O7/c1-30(2)17-6-9-21-23(14-17)37-24-15-18(31(3)4)7-10-22(24)29(21)20-8-5-16(13-19(20)28(36)38-29)27(35)39-32-25(33)11-12-26(32)34/h5-10,13-15H,11-12H2,1-4H3
• InChI key: CXYYHBMOVJJZTD-UHFFFAOYSA-N

Description

Application

5(6)-Carboxytetramethylrhodamine N-succinimidyl ester (TMR-SE) is used as an amine coupling reagent to form 5(6)-carboxytetramethylrhodamine (TMR) derivatized compounds such as proteins and drugs.

Packaging

Bottomless glass bottle. Contents are inside inserted fused cone.

Other Notes

Rhodamine derived label for amine modification and protein conjugation

Informations sur la sécurité

• Classe de stockage: 11 - Combustible Solids
• wgk: WGK 3
• flash_point_f: Not applicable
• flash_point_c: Not applicable
• ppe: Eyeshields, Gloves, type N95 (US)