8.52068

Fmoc-(FmocHmb)Lys(Boc)-OH

Novabiochem®

Manufacturer: Sigma Aldrich

CAS Number: 166881-56-7

Synonym(S): Fmoc-(FmocHmb)Lys(Boc)-OH, N-α-Fmoc-N-α-(2-Fmoc-oxy-4-methoxybenzyl)-N-ε-t.-butoxycarbonyl-L-lysine

Select a Size

Pack Size SKU Availability Price
5 G 8.52068-5-G In Stock ₹ 75,610.01

8.52068 - 5 G

₹ 75,610.01

In Stock

Quantity

1

Base Price: ₹ 75,610.01

GST (18%): ₹ 13,609.802

Total Price: ₹ 89,219.812

Quality Level

200

product line

Novabiochem®

Assay

≥97.0% (HPLC)≥98% (TLC)

form

powder

reaction suitability

reaction type: Fmoc solid-phase peptide synthesis

manufacturer/tradename

Novabiochem®

application(s)

peptide synthesis

functional group

Bocamine

storage temp.

2-8°C

InChI

1S/C49H50N2O10/c1-49(2,3)61-46(54)50-26-14-13-23-43(45(52)53)51(47(55)58-29-41-37-19-9-5-15-33(37)34-16-6-10-20-38(34)41)28-31-24-25-32(57-4)27-44(31)60-48(56)59-30-42-39-21-11-7-17-35(39)36-18-8-12-22-40(36)42/h5-12,15-22,24-25,27,41-43H,13-14,23,26,28-30H2,1-4H3,(H,50,54)(H,52,53)/t43-/m0/s1

Description

  • General description: Hmb protection of amide bonds has been shown to inhibit aggregation of "difficult" peptides by Fmoc SPPS, thereby leading to products of increased purity [1,2,3,4,5,6]. Retention of Hmb groups on the cleaved peptide can greatly improve the solubility of protected peptide fragments [7,8] and otherwise intractable sequences [9,10,11]. Furthermore, using a Hmb-protected derivative for incorporation of the residue linked to the carboxy group of Asp or Asn residues has been found to suppress formation of aspartimide and piperidide related by-products [12,11,14]. For a comparison of the efficiency of Hmb and pseudoprolines in preventing aggregation, see [15]. Associated Protocols and Technical ArticlesCleavage and Deprotection Protocols for Fmoc SPPSLiterature references[1] T. Johnson, et al. (1993) J. Chem. Soc., Chem. Commun., 369. [2] C. Hyde, et al. (1994) Int. J. Peptide Protein Res., 43, 431. [3] L. C. Packman, et al. (1994) Pept. Res., 7, 125. [4] T. Johnson, et al. (1994) Tetrahedron Lett., 35, 463. [5] R. G. Simmonds (1996) Int. J. Peptide Protein Res., 47, 36. [6] T. Johnson, et al. (1995) Lett. Pept. Sci., 1, 11. [7] M. Quibell, et al. (1995) J. Am. Chem. Soc., 117, 11656. [8] M. Quibell, et al. (1996) J. Chem. Soc., Perkin Trans. 1, 1227. [9] M. Quibell, et al. (1994) Tetrahedron Lett., 35, 2237. [10] M. Quibell, et al. (1994) J. Org. Chem., 59, 1745. [11] M. Quibell, et al. (1995) J. Chem. Soc., Perkin Trans. 1, 2019. [12] M. Quibell, et al. (1994) J. Chem. Soc., Chem. Commun., 2343. [13] L. C. Packman (1995) Tetrahedron Lett., 36, 7523. [14] J. Offer, et al. (1996) J. Chem. Soc., Perkin Trans. 1, 175. [15] W. R. Sampson, et al. (1999) J. Peptide Sci., 5, 403.
  • Linkage: Replaces: 04-12-1148
  • Analysis Note: Color (visual): white to slight yellow to beigeAppearance of substance (visual): powderIdentity (IR): passes testEnantiomeric purity: ≥ 99.5 % (a/a)Purity (TLC(157A)): ≥ 98 %Purity (TLC(157B)): ≥ 98 %Assay (HPLC, area%): ≥ 97.0 % (a/a)Solubility (1 mmole in 2 ml DMF): clearly solubleTo see the solvent systems used for TLC of Novabiochem® products please click here.
  • Legal Information: Novabiochem is a registered trademark of Merck KGaA, Darmstadt, Germany

SAFETY INFORMATION

Storage Class Code

11 - Combustible Solids

WGK

WGK 2

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

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8.52068

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Quality Level:
200

product line:
Novabiochem®

Assay:
≥97.0% (HPLC)≥98% (TLC)

form:
powder

reaction suitability:
reaction type: Fmoc solid-phase peptide synthesis

manufacturer/tradename:
Novabiochem®

application(s):
peptide synthesis

functional group:
Bocamine

storage temp.:
2-8°C

InChI:
1S/C49H50N2O10/c1-49(2,3)61-46(54)50-26-14-13-23-43(45(52)53)51(47(55)58-29-41-37-19-9-5-15-33(37)34-16-6-10-20-38(34)41)28-31-24-25-32(57-4)27-44(31)60-48(56)59-30-42-39-21-11-7-17-35(39)36-18-8-12-22-40(36)42/h5-12,15-22,24-25,27,41-43H,13-14,23,26,28-30H2,1-4H3,(H,50,54)(H,52,53)/t43-/m0/s1

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Sigma Aldrich

8.52069

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Quality Level:
200

product line:
Novabiochem®

Assay:
≥90.0% (acidimetric)≥95.0% (HPLC)≥97% (TLC)

form:
powder

reaction suitability:
reaction type: Fmoc solid-phase peptide synthesis

manufacturer/tradename:
Novabiochem®

application(s):
peptide synthesis

functional group:
Fmoc

storage temp.:
−20°C (−15°C to −25°C)

InChI:
__

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Sigma Aldrich

8.52070

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200

product line:
Novabiochem®

Assay:
≥90.0% (acidimetric)≥98% (TLC)≥98.0% (HPLC)

form:
powder

reaction suitability:
reaction type: Fmoc solid-phase peptide synthesis

manufacturer/tradename:
Novabiochem®

application(s):
peptide synthesis

functional group:
Fmoc

storage temp.:
15-25°C

InChI:
1S/C26H26NO8P/c1-17(35-36(31,32)34-15-18-9-3-2-4-10-18)24(25(28)29)27-26(30)33-16-23-21-13-7-5-11-19(21)20-12-6-8-14-22(20)23/h2-14,17,23-24H,15-16H2,1H3,(H,27,30)(H,28,29)(H,31,32)/t17-,24+/m0/s1

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Sigma Aldrich

8.52071

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Quality Level:
200

product line:
Novabiochem®

Assay:
≥90.0% (acidimetric)≥95% (TLC)≥95.0% (HPLC)

form:
powder

reaction suitability:
reaction type: Fmoc solid-phase peptide synthesis

manufacturer/tradename:
Novabiochem®

application(s):
peptide synthesis

functional group:
Fmoc

storage temp.:
__

InChI:
__