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00920

Sigma-Aldrich

N-Acetyl-L-aspartic acid

≥99.0% (T)

Sinonimo/i:

(2S)-2-Acetamidobutanedioic acid, N-Acetyl-S-aspartic acid

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About This Item

Formula condensata:
HO2CCH2CH(NHCOCH3)CO2H
Numero CAS:
Peso molecolare:
175.14
Beilstein:
1726198
Numero MDL:
Codice UNSPSC:
12352209
eCl@ss:
32160406
ID PubChem:
NACRES:
NA.22

Livello qualitativo

Saggio

≥99.0% (T)

Forma fisica

powder

Attività ottica

[α]20/D +12±1°, c = 2% in 6 M HCl

Impiego in reazioni chimiche

reaction type: solution phase peptide synthesis

Colore

colorless to white

Punto di fusione

137-140 °C (lit.)
141-146 °C

applicazioni

peptide synthesis

Stringa SMILE

CC(=O)N[C@@H](CC(O)=O)C(O)=O

InChI

1S/C6H9NO5/c1-3(8)7-4(6(11)12)2-5(9)10/h4H,2H2,1H3,(H,7,8)(H,9,10)(H,11,12)/t4-/m0/s1
OTCCIMWXFLJLIA-BYPYZUCNSA-N

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Applicazioni

N-Acetyl-L-aspartic acid can be used as a reactant to synthesize:
  • Protected homoserine γ-lactones by selective reduction and acid-catalyzed cyclization reaction.
  • Racemic amino substituted succinimide derivatives via cyclocondensation reaction.

Altre note

Review; acetyl donor in acetylcholine formation in brain.

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

Eyeshields, Gloves, type N95 (US)


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