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Merck

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8.55046

IIDQ-polystyrene

Novabiochem®

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A ustedes/SKUDisponibilidadPrecio
5 g
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300,00 €
25 g
Póngase en contacto con nuestro Servicio de Atención al Cliente para disponibilidad
1180,00 €

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NACRES:
NA.22
UNSPSC Code:
13111023

300,00 €


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Quality Segment

product line

Novabiochem®

form

beads

reaction suitability

reaction type: solution phase peptide synthesis

manufacturer/tradename

Novabiochem®

application(s)

peptide synthesis

storage temp.

2-8°C

General description

IIDQ-polystyrene (IIDQ-PS) [1] is a polymer-supported version of the IIDQ coupling reagent [2]. IIDQ has many advantages over conventional carbodiimide- or uronium-based reagents: no preactivation step is required, and acid, amine and coupling reagent can be added in any order; in contrast to uronium-based reagents like HBTU, it cannot form guanidinium by-products; and it is totally stable to base. The treatment of a carboxylic acid with IIDQ-PS in DCM or MeCN rapidly generates in situ the corresponding isobutoxycarbonyl mixed anhydride [3]. Attack by nucleophiles preferentially takes place at the less hindered and more electrophilic carbonyl of the carboxylic acid moiety, releasing only volatile carbon dioxide and isobutanol as by-products. If reaction is carried out in the presence of an amine, amide bond formation occurs concurrently with generation of the anhydride. Alternatively, addition of NaBH4 or polymer-supported borohydride to the anhydride will lead directly to the corresponding alcohol. IIDQ-PS appears to be particularly effective for mediating the acylation for anilines, and has also been found to couple peptide fragments without epimerization. In a comparative study, IIDQ-PS was found to give higher yields and greater purities than HATU, EDC-PS or DCC-PS [4]. Occasionally, with some secondary amines the formation of isobutyl carbamate by-products has been observed, resulting from attack by the amine at the carbonyl group.

Literature references

[1] E. Valeur, et al. (2005) Chem. Commun., 1164.
[2] Y. Kiso, et al. (1973) Chem. Pharm. Bull., 21, 2507.
[3] J. R. Vaughan (1951) J. Am. Chem. Soc., 73, 3547.
[4] E. Valeur & M. Bradley, unpublished results.

Analysis Note

Color (visual): yellow to beige to amber
Appearance of substance (visual): beads
Loading (determined by HPLC after reaction of 3-phenylpropionic acid with cyclohexlamine): 1.3 - 1.9 mmol/g
Swelling Volume (in DMF): lot specific result
The polymer matrix is copoly (styrene-1 % DVB) 200 - 400 mesh.

Other Notes

Replaces: 01-64-0469

Legal Information

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

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Este artículo
8.510958.550438.55029
reaction suitability

reaction type: solution phase peptide synthesis

reaction suitability

reaction type: Coupling Reactions

reaction suitability

reaction type: solution phase peptide synthesis, reactivity: alcohol reactive

reaction suitability

reaction type: solution phase peptide synthesis, reactivity: carboxyl reactive

product line

Novabiochem®

product line

Novabiochem®

product line

Novabiochem®

product line

Novabiochem®

Quality Level

200

Quality Level

300

Quality Level

200

Quality Level

200

application(s)

peptide synthesis

application(s)

peptide synthesis

application(s)

peptide synthesis

application(s)

peptide synthesis

storage temp.

2-8°C

storage temp.

-10 to -25°C

storage temp.

2-8°C

storage temp.

2-8°C

form

beads

form

powder

form

beads

form

beads


Clase de almacenamiento

11 - Combustible Solids

wgk

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable



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