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531480

Sigma-Aldrich

Fmoc-Ala-OH

95%, for peptide synthesis

Sinônimo(s):

N-(9-Fluorenylmethoxycarbonyl)-L-alanine, Fmoc-L-alanine

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About This Item

Fórmula empírica (Notação de Hill):
C18H17NO4
Número CAS:
35661-39-3
Peso molecular:
311.33
Beilstein:
2225975
Número CE:
252-660-6
Número MDL:
MFCD00037139
Código UNSPSC:
12352209
ID de substância PubChem:
24877820
NACRES:
NA.26

product name

Fmoc-Ala-OH, 95%

Nível de qualidade

100

Ensaio

95%

atividade óptica

[α]20/D −18°, c = 1 in DMF

adequação da reação

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

pf

147-153 °C (lit.)

aplicação(ões)

peptide synthesis

grupo funcional

Fmoc
amine
carboxylic acid

temperatura de armazenamento

2-8°C

cadeia de caracteres SMILES

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

InChI

1S/C18H17NO4/c1-11(17(20)21)19-18(22)23-10-16-14-8-4-2-6-12(14)13-7-3-5-9-15(13)16/h2-9,11,16H,10H2,1H3,(H,19,22)(H,20,21)/t11-/m0/s1

chave InChI

QWXZOFZKSQXPDC-NSHDSACASA-N

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Descrição geral

Fmoc-Ala-OH also known as Fmoc-L-alanine, is a versatile reagent used in Fmoc solid-phase peptide synthesis.

Aplicação

Fmoc-Ala-OH is commonly used :
  • as a building block in the preparation of triazolopeptides , and azapeptides
  • in the synthesis of bis-cationic porphyrin peptides using the standard Fmoc solid-phase synthesis
  • to transform Mannich-adducts into α-halogenated amides without undergoing aziridination

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Equipamento de proteção individual

Eyeshields, Gloves, type N95 (US)

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Certificados de análise (COA)

Lot/Batch Number
STBK8567
STBK8241
STBK1840
STBJ8127
STBJ0464

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