Skip to Content
Merck
All Photos(1)

Key Documents

View All Documentation

A4003

Sigma-Aldrich

Ala-Tyr

≥98% (TLC), suitable for mass spectrometry (MS)

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Empirical Formula (Hill Notation):
C12H16N2O4
CAS Number:
3061-88-9
Molecular Weight:
252.27
EC Number:
221-305-7
MDL number:
MFCD00038164
UNSPSC Code:
12352202
PubChem Substance ID:
24890736
NACRES:
NA.26

product name

Ala-Tyr,

Assay

≥98% (TLC)

form

powder

technique(s)

mass spectrometry (MS): suitable

color

white

storage temp.

−20°C

SMILES string

C[C@H](N)C(=O)N[C@@H](Cc1ccc(O)cc1)C(O)=O

InChI

1S/C12H16N2O4/c1-7(13)11(16)14-10(12(17)18)6-8-2-4-9(15)5-3-8/h2-5,7,10,15H,6,13H2,1H3,(H,14,16)(H,17,18)/t7-,10-/m0/s1

InChI key

ALZVPLKYDKJKQU-XVKPBYJWSA-N

Gene Information

human ... SLC15A1(6564)

Looking for similar products? Visit Product Comparison Guide

Related Categories

Amino Acid Sequence

Ala-Tyr

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

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Efficient preparation and biological evaluation of a novel multivalency bifunctional chelator for 64Cu radiopharmaceuticals.
Shuanglong Liu et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 17(37), 10222-10225 (2011-08-05)
Manuela Hammitzsch-Wiedemann et al.
Analytical chemistry, 81(21), 8765-8773 (2009-10-09)
A separation selectivity model for capillary electrophoresis enantioseparations of weak bases in the presence of uncharged chiral selectors was described as a function of buffer pH and chiral selector concentration. On the basis of the selectivity at the extreme pH
Y Kano et al.
Journal of biochemistry, 95(4), 1041-1046 (1984-04-01)
The fat body of Sarcophaga peregrina larvae was found to have activity for synthesis of sarcophagine (beta-alanyl-L-tyrosine). This activity was due to a soluble enzyme (sarcophagine synthetase) that requires Mg2+ and ATP as cofactors. The enzyme activity decreased significantly after
T J Wadas et al.
Current pharmaceutical design, 13(1), 3-16 (2007-02-03)
Molecular imaging is an important scientific discipline that plays a major role in clinical medicine and pharmaceutical development. While several imaging modalities including X-ray computed tomography (CT) and magnetic resonance imaging (MRI) generate high-resolution anatomical images, positron emission tomography (PET)
Yanjun Yang et al.
Journal of agricultural and food chemistry, 55(19), 7891-7895 (2007-08-25)
Corn gluten meal (CGM) was hydrolyzed by Alcalase after starch removal of CGM was applied as a pretreatment. A new inhibitory peptide for angiotensin I-converting enzyme (ACE) was isolated from the hydrolysate of CGM with the use of Bio-Rad P-2
View All Related Papers

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service