Passa al contenuto
Merck
Tutte le immagini(1)

Documenti fondamentali

Visualizza tutta la documentazione

162663

Sigma-Aldrich

DL-2-Aminobutyric acid

99%, for peptide synthesis, ReagentPlus®

Sinonimo/i:

AABA, Homoalanine, alpha-amino-n-butyric acid

Autenticatiper visualizzare i prezzi riservati alla tua organizzazione & contrattuali
Tutte le immagini(1)

About This Item

Formula condensata:
C2H5CH(NH2)CO2H
Numero CAS:
2835-81-6
Peso molecolare:
103.12
Beilstein:
635889
Numero CE:
220-616-5
Numero MDL:
MFCD00008093
Codice UNSPSC:
12352116
ID PubChem:
24849999
NACRES:
NA.22

Nome del prodotto

DL-2-Aminobutyric acid, ReagentPlus®, 99%

Livello qualitativo

200

Nome Commerciale

ReagentPlus®

Saggio

99%

Stato

solid

Impiego in reazioni chimiche

reaction type: solution phase peptide synthesis

Punto di fusione

291 °C (dec.) (lit.)

applicazioni

peptide synthesis

Stringa SMILE

CCC(N)C(O)=O

InChI

1S/C4H9NO2/c1-2-3(5)4(6)7/h3H,2,5H2,1H3,(H,6,7)
QWCKQJZIFLGMSD-UHFFFAOYSA-N

Cerchi prodotti simili? Visita Guida al confronto tra prodotti

Descrizione generale

DL-2-Aminobutyric acid also known as α-aminobutyric acid, is commonly used in solution-phase peptide synthesis.

Applicazioni

DL-2-Aminobutyric acid can be used to synthesize 2-(2,5-dioxopyrrolidin-1-yl) butanoic acid.

Note legali

ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany

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)

Scegli una delle versioni più recenti:

Certificati d'analisi (COA)

Lot/Batch Number
BCCG8786
BCCG8195
BCCD1594
BCBL7245V
BCBB2521V

Non trovi la versione di tuo interesse?

Se hai bisogno di una versione specifica, puoi cercare il certificato tramite il numero di lotto.

Cerca un COA

Possiedi già questo prodotto?

I documenti relativi ai prodotti acquistati recentemente sono disponibili nell’Archivio dei documenti.

Visita l’Archivio dei documenti

I clienti hanno visto anche

Slide 1 of 5

1 of 5

DL-Norleucine

Sigma-Aldrich

N1398

DL-Norleucine

4-Aminobutyric acid for synthesis

Sigma-Aldrich

8.00302

4-Aminobutyric acid

β-Alanine BioXtra, ≥99.0% (NT)

Sigma-Aldrich

05160

β-Alanine

NG,NG-Dimethylarginine dihydrochloride

Sigma-Aldrich

D4268

NG,NG-Dimethylarginine dihydrochloride

2-Aminobenzaldehyde ≥98%

Sigma-Aldrich

A9628

2-Aminobenzaldehyde

Ryan J Martinie et al.
Journal of the American Chemical Society, 137(21), 6912-6919 (2015-05-13)
The iron(II)- and 2-(oxo)glutarate-dependent (Fe/2OG) oxygenases catalyze an array of challenging transformations, but how individual members of the enzyme family direct different outcomes is poorly understood. The Fe/2OG halogenase, SyrB2, chlorinates C4 of its native substrate, l-threonine appended to the
Fatemeh Mahmoodani et al.
Journal of food science and technology, 51(9), 1847-1856 (2014-09-06)
Skin and bone gelatins of pangasius catfish (Pangasius sutchi) were hydrolyzed with alcalase to isolate Angiotensin Converting Enzyme (ACE) inhibitory peptides. Samples with the highest degree of hydrolysis (DH) were separated into different fractions with molecular weight cut-off (MWCO) sizes
Christian Rausch et al.
Proteins, 81(5), 774-787 (2012-12-15)
Apart from their crucial role in metabolism, pyridoxal 5'-phosphate (PLP)-dependent aminotransferases (ATs) constitute a class of enzymes with increasing application in industrial biotechnology. To provide better insight into the structure-function relationships of ATs with biotechnological potential we performed a fundamental
Kun Huang et al.
The Journal of biological chemistry, 282(48), 35337-35349 (2007-09-22)
The contribution of the insulin A-chain to receptor binding is investigated by photo-cross-linking and nonstandard mutagenesis. Studies focus on the role of Val(A3), which projects within a crevice between the A- and B-chains. Engineered receptor alpha-subunits containing specific protease sites
Young-Man Seo et al.
Organic & biomolecular chemistry, 10(12), 2482-2485 (2012-02-22)
A deracemization method was developed to generate optically pure L-homoalanine from racemic homoalanine using D-amino acid oxidase and ω-transaminase. A whole cell reaction using a biphasic system converted 500 mM racemic homoalanine to 485 mM L-homoalanine (>99% ee).
Visualizza tutti i documenti correlati

Il team dei nostri ricercatori vanta grande esperienza in tutte le aree della ricerca quali Life Science, scienza dei materiali, sintesi chimica, cromatografia, discipline analitiche, ecc..

Contatta l'Assistenza Tecnica.