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47594

Sigma-Aldrich

Fmoc-N-Me-Ala-OH

≥97.0% (sum of enantiomers, HPLC)

Synonym(s):

Fmoc-N-methyl-L-alanine

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1 G
$107.00

About This Item

Empirical Formula (Hill Notation):
C19H19NO4
CAS Number:
Molecular Weight:
325.36
Beilstein/REAXYS Number:
4329998
MDL number:
UNSPSC Code:
12352209
eCl@ss:
32160406
PubChem Substance ID:
NACRES:
NA.26

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assay

≥97.0% (sum of enantiomers, HPLC)

optical activity

[α]20/D −18.5±1°, c = 1% in DMF

reaction suitability

reaction type: Fmoc solid-phase peptide synthesis

application(s)

peptide synthesis

functional group

Fmoc

storage temp.

2-8°C

SMILES string

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

InChI

1S/C19H19NO4/c1-12(18(21)22)20(2)19(23)24-11-17-15-9-5-3-7-13(15)14-8-4-6-10-16(14)17/h3-10,12,17H,11H2,1-2H3,(H,21,22)/t12-/m0/s1

InChI key

JOFHWKQIQLPZTC-LBPRGKRZSA-N

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1 of 4

This Item
4777253148017313
assay

≥97.0% (sum of enantiomers, HPLC)

assay

≥98.0% (HPLC)

assay

95%

assay

≥95.0% (HPLC)

functional group

Fmoc

functional group

Fmoc

functional group

Fmoc, amine, carboxylic acid

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

100

optical activity

[α]20/D −18.5±1°, c = 1% in DMF

optical activity

-

optical activity

[α]20/D −18°, c = 1 in DMF

optical activity

-

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

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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