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Documentos Principais

47639

Sigma-Aldrich

Fmoc-His(Trt)-OH

≥98.0% (sum of enantiomers, HPLC), for peptide synthesis

Sinônimo(s):

Nα-Fmoc-N(im)-trityl-L-histidine

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About This Item

Fórmula empírica (Notação de Hill):
C40H33N3O4
Número CAS:
Peso molecular:
619.71
Beilstein:
5204720
Número MDL:
Código UNSPSC:
12352209
eCl@ss:
32160406
ID de substância PubChem:
NACRES:
NA.26

Nome do produto

Fmoc-His(Trt)-OH, ≥98.0% (sum of enantiomers, HPLC)

Ensaio

≥98.0% (sum of enantiomers, HPLC)

atividade óptica

[α]/D 87±5°, c = 1 in chloroform

adequação da reação

reaction type: Fmoc solid-phase peptide synthesis

aplicação(ões)

peptide synthesis

grupo funcional

Fmoc

temperatura de armazenamento

2-8°C

cadeia de caracteres SMILES

OC(=O)[C@H](Cc1cn(cn1)C(c2ccccc2)(c3ccccc3)c4ccccc4)NC(=O)OCC5c6ccccc6-c7ccccc57

InChI

1S/C40H33N3O4/c44-38(45)37(42-39(46)47-26-36-34-22-12-10-20-32(34)33-21-11-13-23-35(33)36)24-31-25-43(27-41-31)40(28-14-4-1-5-15-28,29-16-6-2-7-17-29)30-18-8-3-9-19-30/h1-23,25,27,36-37H,24,26H2,(H,42,46)(H,44,45)/t37-/m0/s1

chave InChI

XXMYDXUIZKNHDT-QNGWXLTQSA-N

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Aplicação

Fmoc-His(Trt)-OH can be used as a building block in solid-phase peptide synthesis (SPPS).

Nota de análise

may contain ~1 equivalent solvent

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Equipamento de proteção individual

Eyeshields, Gloves, type N95 (US)


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With a growing peptide drug market the fast, reliable and uncomplicated synthesis of peptides is of paramount importance.

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