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L3377

Sigma-Aldrich

Leu-D-Leu

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About This Item

Empirische Formel (Hill-System):
C12H24N2O3
CAS-Nummer:
17665-02-0
Molekulargewicht:
244.33
MDL-Nummer:
MFCD00066071
UNSPSC-Code:
12352200
PubChem Substanz-ID:
24896339

Form

solid

Methode(n)

HPLC: suitable
mass spectrometry (MS): suitable

Lagertemp.

−20°C

SMILES String

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

InChI

1S/C12H24N2O3/c1-7(2)5-9(13)11(15)14-10(12(16)17)6-8(3)4/h7-10H,5-6,13H2,1-4H3,(H,14,15)(H,16,17)/t9-,10+/m0/s1

InChIKey

LCPYQJIKPJDLLB-VHSXEESVSA-N

Anwendung

Leu-D-Leu may be used as a reference peptide in the development of separation and detection technologies such as CE-ESI-MS.

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

Eyeshields, Gloves, type N95 (US)

Analysenzertifikate (COA)

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Hongzhi Ye et al.
Electrophoresis, 31(20), 3400-3406 (2010-09-30)
In this article, an approach has been developed for the analysis of some small peptides with similar pI values by CE-ESI-MS based on the online concentration strategy of dynamic pH junction. The factors affected on the separation, detection and online
Joachim Vater et al.
Rapid communications in mass spectrometry : RCM, 23(10), 1493-1498 (2009-04-08)
An innovative technique to investigate the intermediates involved in the biosynthesis of the lipoheptapeptide surfactin from Bacillus subtilis OKB105 combining whole-cell matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOFMS) with targeted generation of knock-out mutants was demonstrated. This method allows efficient
Y K Cho et al.
The Journal of biological chemistry, 273(38), 24305-24308 (1998-09-12)
Porcine pepsin proteolysis of the hexapeptide Leu-Ser-p-nitro-Phe-Nle-Ala-Leu-OMe (where OMe = methoxy and Nle = norleucine) in the presence of dipeptide Leu-Leu synthesizes a new hexapeptide Leu-Ser-p-nitro-Phe-Leu-Leu. Contrary to transpeptidation kinetics of other proteases, which depend upon an acyl-enzyme intermediate, the
S N Mitra et al.
Biopolymers, 34(9), 1139-1143 (1994-09-01)
The crystal structure of a dipeptide L-leucyl-L-leucine (C12H24N2O3) has been determined. The crystals are monoclinic, space group P2(1), with a = 5.434(4) A, b = 15.712(7) A, c = 11.275(2) A, beta = 100.41(1) degrees, and Z = 2. The
Pim W J M Frederix et al.
Dalton transactions (Cambridge, England : 2003), 41(42), 13112-13119 (2012-09-20)
A [FeFe]-hydrogenase model compound (µ-S(CH(2))(3)S)Fe(2)(CO)(4)(PMe(3))(2) [1] has been encapsulated in a low molecular weight (LMW) hydrogelator (Fmoc-Leu-Leu). Linear infrared absorption spectroscopy, gel melting and ultrafast time-resolved infrared spectroscopy experiments reveal significant contrasts in chemical environment and photochemistry between the encapsulated
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