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Key Documents

47601

Sigma-Aldrich

Fmoc-Ser-OH

≥97.0% (sum of enantiomers, HPLC)

Synonym(s):

Fmoc-L-serine

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About This Item

Empirical Formula (Hill Notation):
C18H17NO5
CAS Number:
Molecular Weight:
327.33
Beilstein/REAXYS Number:
4715791
MDL number:
UNSPSC Code:
12352209
PubChem Substance ID:

Quality Level

assay

≥97.0% (sum of enantiomers, HPLC)

optical activity

[α]20/D −12.5±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

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

InChI

1S/C18H17NO5/c20-9-16(17(21)22)19-18(23)24-10-15-13-7-3-1-5-11(13)12-6-2-4-8-14(12)15/h1-8,15-16,20H,9-10H2,(H,19,23)(H,21,22)/t16-/m0/s1

InChI key

JZTKZVJMSCONAK-INIZCTEOSA-N

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)


Certificates of Analysis (COA)

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Peiming Chen et al.
Journal of controlled release : official journal of the Controlled Release Society, 194, 341-349 (2014-09-16)
Macrophages are involved in a number of diseases, such as HIV infection/AIDS, tuberculosis, tumor development and atherosclerosis. Macrophages possess several cell surface receptors (e.g., the mannose receptor, MR) that may serve as drug delivery cellular portals for nanocarriers (NCs). In

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