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FMOC-Ala-OH

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FMOC-Ala-OH Basic information

Product Name:
FMOC-Ala-OH
Synonyms:
  • N-ALPHA-(9-FLUORENYLMETHOXYCARBONYL)-L-ALANINE
  • N-ALPHA-(9-FLUORENYLMETHYLOXYCARBONYL)-L-ALANINE
  • N-ALPHA-FMOC-L-ALA
  • N-ALPHA-FMOC-L-ALANINE
  • Fmoc-DL-Alanine
  • L-ALANINE-2-13C, N-FMOC DERIV 99&
  • Fmoc-L-alanine,98%
  • L-Alanine-2-13C-N-FMOC
CAS:
35661-39-3
MF:
C18H17NO4
MW:
311.33
EINECS:
252-660-6
Product Categories:
  • Fmoc-Amino acid series
  • Alanine [Ala, A]
  • Protected Amino Acids
  • Fluorenes, Flurenones
  • Amino Acids
  • Fmoc-Amino Acids and Derivatives
  • Amino Acids (N-Protected)
  • Biochemistry
  • Fmoc-Amino Acids
Mol File:
35661-39-3.mol
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FMOC-Ala-OH Chemical Properties

Melting point:
147-153 °C (lit.)
alpha 
-19 º (c=1,DMF)
Boiling point:
451.38°C (rough estimate)
Density 
1.2626 (rough estimate)
refractive index 
-18.5 ° (C=1, DMF)
storage temp. 
Store below +30°C.
solubility 
DMSO (Slightly), DMF (Sparingly), Methanol (Slightly)
form 
Solid
pka
3.91±0.10(Predicted)
color 
White
optical activity
[α]20/D 18°, c = 1 in DMF
Water Solubility 
Soluble in water.
BRN 
2225975
InChIKey
QWXZOFZKSQXPDC-NSHDSACASA-N
CAS DataBase Reference
35661-39-3(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
24/25-36/37/39-27-26
WGK Germany 
3
HazardClass 
IRRITANT
HS Code 
29242990

MSDS

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FMOC-Ala-OH Usage And Synthesis

Chemical Properties

white to light yellow crystal powde

Uses

FMOC-Ala-OH is potentially useful for proteomics studies and solid phase peptide synthesis techniques. Alanine is one of the simplest amino acids - a methyl group as the side chain. This small side chain confers a high degree of flexibility when incorporated into a polypeptide chain. The Fmoc group is typically removed with a base such as pyridine - an orthogonal de-protection strategy to the acid labilie Boc group.

Preparation

A solution of the Fmoc-OX derivatives (20 mmol) in 100 mL acetone was added dropwise to a stirred solution of Alanine (20 mmol) and NaHCO(50 mmol) in 100 mL water. After stirring overnight the reaction mixture was concentrated under reduced pressure and then extracted with CH2Cl2 (50 mL) to remove the unreacted Fmoc-OX derivatives. The reaction mixture was cooled and acidified with 10% HCl to congo red litmus paper to give a white solid, which was filtered and washed with water several times, dried to give a white solid (FMOC-Ala-OH).Yield=89.5%.

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