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A1878

Sigma-Aldrich

Ala-Leu

≥99% (TLC)

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About This Item

Empirical Formula (Hill Notation):
C9H18N2O3
CAS Number:
3303-34-2
Molecular Weight:
202.25
EC Number:
221-977-1
MDL number:
MFCD00065106
UNSPSC Code:
12352202
PubChem Substance ID:
24890594
NACRES:
NA.26
Pricing and availability is not currently available.

Product Name

Ala-Leu,

Assay

≥99% (TLC)

Quality Level

200

form

powder

color

white

storage temp.

−20°C

SMILES string

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

InChI

1S/C9H18N2O3/c1-5(2)4-7(9(13)14)11-8(12)6(3)10/h5-7H,4,10H2,1-3H3,(H,11,12)(H,13,14)/t6-,7-/m0/s1

InChI key

RDIKFPRVLJLMER-BQBZGAKWSA-N

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1 of 4

This Item
G327250950PHG0006
Guanidina hydrochloride BioUltra, for molecular biology, ≥99.5% (AT)

50933

Guanidina hydrochloride

Guanidina hydrochloride for molecular biology, ≥99%

G3272

Guanidina hydrochloride

Guanidina hydrochloride ≥98%

50950

Guanidina hydrochloride

Guanidina hydrochloride

PHG0006

Guanidina hydrochloride

grade

for molecular biology

grade

for molecular biology

grade

-

grade

-

assay

≥99.5% (AT)

assay

≥99%

assay

≥98%

assay

-

product line

BioUltra

product line

-

product line

-

product line

-

Quality Level

200

Quality Level

400

Quality Level

200

Quality Level

400

form

powder or crystals

form

crystalline powder

form

powder or crystals

form

powder

Biochem/physiol Actions

Alanyl dipeptides such as ala-leu, ala-lys, ala-gly, ala-pro, ala-tyr and ala-phe may be used in physicochemical studies or to evaluate dipeptide separation technologies. Alanyl dipeptides may also be used for studying cell uptake mechanisms, dipeptide metabolism or cell growth supplementation benefits.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves
  • Specification Sheet

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    Certificates of Analysis (COA)

    Lot/Batch Number
    BCCF0047
    BCCB6890
    BCBT9748
    BCBS0882V
    BCBN9071V

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    Matthew Rosati et al.
    Molecular and biochemical parasitology, 217, 7-12 (2017-08-16)
    The aminopeptidase PfA-M1 is a key contributor to peptide catabolism in the human malaria parasite Plasmodium falciparum. PfA-M1 substrate specificity is shaped by the cylindrical S1 subsite, which accommodates the sidechain of the substrate P1 residue. At the top of
    Alice B Nongonierma et al.
    Food research international (Ottawa, Ont.), 94, 79-89 (2017-03-16)
    The release of dipeptidyl peptidase IV (DPP-IV) inhibitory peptides from bovine milk protein isolate (MPI) during trypsin hydrolysis was studied using a design of experiments (DOE) approach. A 3 factor×3 level DOE including temperature (40, 50 and 60°C), enzyme to
    Víctor Cruz et al.
    The journal of physical chemistry. B, 115(16), 4880-4886 (2011-04-08)
    An exhaustive umbrella sampling simulation of the alanine dipeptide in solution is reported. The presence of stable Y conformations in solution is assessed by both quantum calculations and experimental data from X-ray and NMR protein-solved structures available in the protein
    Voislav Blagojevic et al.
    Analytical chemistry, 83(9), 3470-3476 (2011-04-21)
    The ability to resolve isomeric protonated dipeptides was investigated with the new technique of differential ion mobility mass spectrometry that uses "modifier" molecules to enhance differential mobility. Two pairs of protonated peptides [glycine-alanine (GlyAla) and alanine-glycine (AlaGly), glycine-serine (GlySer) and
    Marie-Pierre Gaigeot
    Physical chemistry chemical physics : PCCP, 12(35), 10198-10209 (2010-06-12)
    Following our previous work [J. Phys. Chem. B. Lett., 2009, 113, 10059], DFT-based molecular dynamics (DFTMD) simulations of 2-Ala peptide (i.e. Ac-Ala-NHMe dialanine peptide analog with methyl group caps at the extremities) immersed in liquid water at room temperature are
    View All Related Papers

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