Merck
All Photos(4)

160512

Sigma-Aldrich

Fmoc chloride

97%

Synonym(s):
9-Fluorenylmethoxycarbonyl chloride, 9-Fluorenylmethyl chloroformate, Fmoc-Cl
Empirical Formula (Hill Notation):
C15H11ClO2
CAS Number:
Molecular Weight:
258.70
Beilstein:
2279177
EC Number:
MDL number:
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

97%

form

solid

mp

62-64 °C (lit.)

application(s)

peptide synthesis

functional group

Fmoc

storage temp.

2-8°C

SMILES string

ClC(=O)OCC1c2ccccc2-c3ccccc13

InChI

1S/C15H11ClO2/c16-15(17)18-9-14-12-7-3-1-5-10(12)11-6-2-4-8-13(11)14/h1-8,14H,9H2

InChI key

IRXSLJNXXZKURP-UHFFFAOYSA-N

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PHR2486M4880383147
Fmoc chloride 97%

Sigma-Aldrich

160512

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assay

97%

assay

-

assay

≥97.0%

assay

≥96.0%

form

solid

form

solid

form

powder

form

powder

mp

62-64 °C (lit.)

mp

-

mp

714 °C (lit.)

mp

772 °C (lit.)

functional group

Fmoc

functional group

-

functional group

-

functional group

-

storage temp.

2-8°C

storage temp.

2-30°C

storage temp.

-

storage temp.

-

Quality Level

200

Quality Level

-

Quality Level

300

Quality Level

200

Application

Amino acid derivatizing agent for HPLC analysis. N-protecting reagent for peptide and oligonucleotide syntheses.
Reagent for amino group protection recently used in the synthesis of a bicyclic proline analog.
Reagent for derivatizing amino acids for HPLC amino acid analysis and for preparing N-Fmoc amino acids for solid-phase peptide synthesis.

Pictograms

Corrosion

Signal Word

Danger

Hazard Statements

Hazard Classifications

Eye Dam. 1 - Skin Corr. 1B

Supplementary Hazards

Storage Class Code

8A - Combustible, corrosive hazardous materials

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificate of Analysis

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Certificate of Origin

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