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16905

Sigma-Aldrich

Fmoc-D-Ile-OH

≥96.0% (HPLC), for peptide synthesis

Synonym(s):

Fmoc-D-isoleucine

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About This Item

Empirical Formula (Hill Notation):
C21H23NO4
CAS Number:
Molecular Weight:
353.41
MDL number:
UNSPSC Code:
12352209
eCl@ss:
32160406
PubChem Substance ID:
NACRES:
NA.26

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Product Name

Fmoc-D-Ile-OH, ≥96.0% (HPLC)

Quality Level

assay

≥96.0% (HPLC)

form

solid

reaction suitability

reaction type: Fmoc solid-phase peptide synthesis

application(s)

peptide synthesis

functional group

Fmoc

SMILES string

CC[C@@H](C)[C@@H](NC(=O)OCC1c2ccccc2-c3ccccc13)C(O)=O

InChI

1S/C21H23NO4/c1-3-13(2)19(20(23)24)22-21(25)26-12-18-16-10-6-4-8-14(16)15-9-5-7-11-17(15)18/h4-11,13,18-19H,3,12H2,1-2H3,(H,22,25)(H,23,24)/t13-,19-/m1/s1

InChI key

QXVFEIPAZSXRGM-BFUOFWGJSA-N

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This Item
8.521634762847319
form

solid

form

powder

form

solid

form

solid

assay

≥96.0% (HPLC)

assay

≥95.0% (acidimetric), ≥98% (TLC), ≥98.0% (HPLC)

assay

≥98.0% (T)

assay

≥98.0% (HPLC)

functional group

Fmoc

functional group

Fmoc

functional group

Fmoc, amine, carboxylic acid

functional group

Fmoc

Quality Level

100

Quality Level

200

Quality Level

100

Quality Level

100

reaction suitability

reaction type: Fmoc solid-phase peptide synthesis

reaction suitability

reaction type: Fmoc solid-phase peptide synthesis

reaction suitability

reaction type: C-H Activation, reaction type: Fmoc solid-phase peptide synthesis, reagent type: ligand
reaction type: Peptide Synthesis

reaction suitability

reaction type: Fmoc solid-phase peptide synthesis

application(s)

peptide synthesis

application(s)

peptide synthesis

application(s)

peptide synthesis

application(s)

peptide synthesis

General description

Fmoc-D-Ile-OH is an amino acid in which Fmoc is a protected form of D-Isoleucine.[1]

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


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