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8.52182

Fmoc-Tyr(tBu)-Thr(psiMe,Mepro)-OH

Novabiochem®

Synonyme(s) :

Fmoc-Tyr(tBu)-Thr(psiMe,Mepro)-OH

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ConditionnementRéférenceDisponibilitéPrix
5 g
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378,00 €

A propos de cet article

Formule empirique (notation de Hill) :
C35H40N2O7
Numéro CAS:
Poids moléculaire :
600.70
MDL number:
UNSPSC Code:
12352209
NACRES:
NA.22

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Quality Level

product line

Novabiochem®

assay

≥97% (TLC), ≥97.0% (HPLC)

form

powder

reaction suitability

reaction type: Fmoc solid-phase peptide synthesis

manufacturer/tradename

Novabiochem®

application(s)

peptide synthesis

functional group

hydroxyl

storage temp.

2-8°C

SMILES string

N5([C@@H]([C@H](OC5(C)C)C)C(=O)O)C(=O)[C@@H](NC(=O)OCC2c3c(cccc3)c4c2cccc4)Cc1ccc(cc1)OC(C)(C)C

InChI

1S/C35H40N2O7/c1-21-30(32(39)40)37(35(5,6)43-21)31(38)29(19-22-15-17-23(18-16-22)44-34(2,3)4)36-33(41)42-20-28-26-13-9-7-11-24(26)25-12-8-10-14-27(25)28/h7-18,21,28-30H,19-20H2,1-6H3,(H,36,41)(H,39,40)/t21-,29+,30+/m1/s1

InChI key

JYSMURJYNLWZNY-RIGQTMPJSA-N

General description

This pseudoproline dipeptide is undoubtedly the most effective and simplest to use tool for overcoming aggregation and enhancing peptide quality in Fmoc SPPS for peptide containing the Tyr-Thr dipeptide motif. It consists of a dipeptide in which the threonine residue has been reversibly protected as a structure-breaking proline-like TFA-labile oxazolidine. The reason the pseudoproline residue is introduced as a dipeptide is because it avoids the need to acylate the hindered oxazolidine nitrogen. This has the added advantage of extending the peptide chain by two residues in one step. The threonine residue is regenerated during the normal TFA-mediated cleavage reaction.

Associated Protocols and Technical Articles
Cleavage and Deprotection Protocols for Fmoc SPPS
Overcoming Aggregation in Fmoc SPPS

Analysis Note

Color (visual): white to slight yellow to beige
Appearance of substance (visual): powder
Identity (IR): passes test
Optical rotation α 25/D (c=1 in methanol): -32.0 - -26.0 °
Purity (TLC(157A)): ≥ 97 %
Purity (TLC(CMA2)): ≥ 97 %
Assay (HPLC, area%): ≥ 97.0 % (a/a)
Single impurities (HPLC, area%): ≤ 1.00 % (a/a)
Ethyl acetate (HS-GC): ≤ 2.0 %
Acetate (IC): ≤ 0.1 %

To see the solvent systems used for TLC of Novabiochem® products please click here.

Other Notes

Replaces: 05-20-1007

Legal Information

Novabiochem is a registered trademark of Merck KGaA, Darmstadt, Germany

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Cet article
8.521808.521818.52178
form

powder

form

powder

form

powder

form

powder

assay

≥97% (TLC), ≥97.0% (HPLC)

assay

≥97% (TLC), ≥97.0% (HPLC)

assay

≥97% (TLC), ≥97.0% (HPLC)

assay

≥97% (TLC), ≥97.0% (HPLC)

functional group

hydroxyl

functional group

hydroxyl

functional group

hydroxyl

functional group

hydroxyl

product line

Novabiochem®

product line

Novabiochem®

product line

Novabiochem®

product line

Novabiochem®

storage temp.

2-8°C

storage temp.

2-8°C

storage temp.

2-8°C

storage temp.

2-8°C

Quality Level

200

Quality Level

200

Quality Level

200

Quality Level

200


Classe de stockage

11 - Combustible Solids

wgk

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable



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Protocoles

The ease of assembly of a given peptide sequence is hard to predict, which makes peptide synthesis challenging. Review methods and reagents for avoiding aggregation in solid-phase peptide synthesis.





Numéro d'article de commerce international

RéférenceGTIN
852182002504027269190316
852182010004027269190293
852182000104027269092702
852182000504027269092719

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