Passa al contenuto
Merck
Tutte le immagini(1)

Documenti fondamentali

Visualizza tutta la documentazione

47628

Sigma-Aldrich

Fmoc-Ile-OH

≥98.0% (T)

Sinonimo/i:

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

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

About This Item

Formula empirica (notazione di Hill):
C21H23NO4
Numero CAS:
71989-23-6
Peso molecolare:
353.41
Beilstein:
4716717
Numero CE:
276-255-9
Numero MDL:
MFCD00037125
Codice UNSPSC:
12352209
eCl@ss:
32160406
ID PubChem:
57651048
NACRES:
NA.26

Saggio

≥98.0% (T)

Stato

solid

Attività ottica

[α]20/D −12±1°, c = 1% in DMF

Impiego in reazioni chimiche

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

Punto di fusione

145-147 °C (lit.)

applicazioni

peptide synthesis

Gruppo funzionale

Fmoc
amine
carboxylic acid

Temperatura di conservazione

2-8°C

Stringa SMILE

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

InChI

1S/C21H23NO4/c1-3-13(2)19(20(23)24)22-21(25)26-12-18-16-10-6-4-8-14(16)15-9-5-7-11-17(15)18/h4-11,13,18-19H,3,12H2,1-2H3,(H,22,25)(H,23,24)/t13-,19-/m0/s1
QXVFEIPAZSXRGM-DJJJIMSYSA-N

Cerchi prodotti simili? Visita Guida al confronto tra prodotti

Categorie correlate

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
BCCD7459
BCCD7457
BCCD5472
BCBZ6720
BCBT4068

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 6

1 of 6

Fmoc-D-Ile-OH ≥96.0% (HPLC)

Sigma-Aldrich

16905

Fmoc-D-Ile-OH

Fmoc-Asp(OtBu)-OH ≥98.0% (HPLC)

Sigma-Aldrich

47618

Fmoc-Asp(OtBu)-OH

Fmoc-Glu(OtBu)-OH ≥98.0% (HPLC)

Sigma-Aldrich

47625

Fmoc-Glu(OtBu)-OH

Fmoc-Tyr(tBu)-OH ≥98.0% (HPLC)

Sigma-Aldrich

47623

Fmoc-Tyr(tBu)-OH

Fmoc-Lys(Boc)-OH ≥98.0% (HPLC)

Sigma-Aldrich

47624

Fmoc-Lys(Boc)-OH

Fmoc-Ser(tBu)-OH ≥98.0% (HPLC)

Sigma-Aldrich

47619

Fmoc-Ser(tBu)-OH

Moise Ndao et al.
Langmuir : the ACS journal of surfaces and colloids, 34(29), 8678-8684 (2016-04-05)
Diatoms are unicellular algae that construct cell walls called frustules by the precipitation of silica, using special proteins that order the silica into a wide variety of nanostructures. The diatom species Cylindrotheca fusiformis contains proteins called silaffins within its frustules
Karthik Nadendla et al.
Molecular pharmaceutics, 16(7), 2922-2928 (2019-05-24)
We have previously described the photoactivated depot (PAD) approach for the light-stimulated release of therapeutic proteins such as insulin. The aim of this method is to release insulin from a shallow dermal depot in response to blood glucose information, using
R Ashton Lavoie et al.
International journal of molecular sciences, 20(7) (2019-04-11)
The growing integration of quality-by-design (QbD) concepts in biomanufacturing calls for a detailed and quantitative knowledge of the profile of impurities and their impact on the product safety and efficacy. Particularly valuable is the determination of the residual level of
R Ashton Lavoie et al.
Biotechnology and bioengineering, 117(2), 438-452 (2019-10-28)
The clearance of host cell proteins (HCPs) is of crucial importance in biomanufacturing, given their diversity in composition, structure, abundance, and occasional structural homology with the product. The current approach to HCP clearance in the manufacturing of monoclonal antibodies (mAbs)
K R Sunil Kumar et al.
ACS nano, 8(5), 4157-4165 (2014-04-01)
To apply motor proteins as natural nanomolecular machines to transporting systems in nanotechnology, complete temporal control over ON/OFF switching of the motility is necessary. We have studied the photoresponsive inhibition properties of azobenzene-tethered peptides for regulation of kinesin-microtubule motility. Although
Visualizza tutti i documenti correlati

Articoli

Natural Amino Acid Building Blocks for Peptide Synthesis

With a growing peptide drug market the fast, reliable and uncomplicated synthesis of peptides is of paramount importance.

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.