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Key Documents

Safety Information

29207

Sigma-Aldrich

Fmoc-Lys(Ddiv)-OH

≥96.0% (HPLC)

Synonym(s):

Nα-Fmoc-Nε-[1-(4,4-dimethyl-2,6-dioxocyclohex-1-ylidene)-3-methylbutyl]-L-lysine

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About This Item

Empirical Formula (Hill Notation):
C34H42N2O6
CAS Number:
Molecular Weight:
574.71
MDL number:
UNSPSC Code:
12352209
PubChem Substance ID:
NACRES:
NA.26

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Assay

≥96.0% (HPLC)

reaction suitability

reaction type: Fmoc solid-phase peptide synthesis

application(s)

peptide synthesis

functional group

Fmoc

storage temp.

2-8°C

SMILES string

CC(C)C\C(NCCCC[C@H](NC(=O)OCC1c2ccccc2-c3ccccc13)C(O)=O)=C4/C(=O)CC(C)(C)CC4=O

InChI

1S/C34H42N2O6/c1-21(2)17-28(31-29(37)18-34(3,4)19-30(31)38)35-16-10-9-15-27(32(39)40)36-33(41)42-20-26-24-13-7-5-11-22(24)23-12-6-8-14-25(23)26/h5-8,11-14,21,26-27,35H,9-10,15-20H2,1-4H3,(H,36,41)(H,39,40)/t27-/m0/s1

InChI key

PYCBVLUBTMHNPW-MHZLTWQESA-N

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1 of 4

This Item
473174757747536
functional group

Fmoc

functional group

Fmoc

functional group

Fmoc

functional group

Fmoc

storage temp.

2-8°C

storage temp.

2-8°C

storage temp.

2-8°C

storage temp.

2-8°C

Quality Level

100

Quality Level

100

Quality Level

100

Quality Level

-

reaction suitability

reaction type: Fmoc solid-phase peptide synthesis

reaction suitability

reaction type: Fmoc solid-phase peptide synthesis

reaction suitability

reaction type: Fmoc solid-phase peptide synthesis

reaction suitability

-

application(s)

peptide synthesis

application(s)

peptide synthesis

application(s)

peptide synthesis

application(s)

peptide synthesis

Other Notes

Orthogonally protected lysine, the Ddiv protection is more stable to piperidine (Fmoc deprotection) than Dde[1]

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

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    S.R. Chhabra et al.
    Tetrahedron Letters, 39, 1603-1603 (1998)

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