Skip to Content
MilliporeSigma
All Photos(1)

Key Documents

View All Documentation

A9627

Sigma-Aldrich

Ala-Ala-Ala

≥98% (TLC)

Synonym(s):

Tri-L-alanine

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

About This Item

Empirical Formula (Hill Notation):
C9H17N3O4
CAS Number:
5874-90-8
Molecular Weight:
231.25
EC Number:
227-538-0
MDL number:
MFCD00025557
UNSPSC Code:
12352209
PubChem Substance ID:
24891479
NACRES:
NA.26
Pricing and availability is not currently available.

Product Name

Ala-Ala-Ala,

assay

≥98% (TLC)

Quality Level

200

form

powder

color

white

storage temp.

−20°C

SMILES string

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

InChI

1S/C9H17N3O4/c1-4(10)7(13)11-5(2)8(14)12-6(3)9(15)16/h4-6H,10H2,1-3H3,(H,11,13)(H,12,14)(H,15,16)/t4-,5-,6-/m0/s1

InChI key

BYXHQQCXAJARLQ-ZLUOBGJFSA-N

Looking for similar products? Visit Product Comparison Guide

Related Categories

Compare Similar Items

View Full Comparison

Show Differences

1 of 4

This Item
A9502A5025A2628
Ala-Ala-Ala

A9627

Ala-Ala-Ala

Ala-Ala

A9502

Ala-Ala

Ala-Ala-Ala-Ala-Ala

A5025

Ala-Ala-Ala-Ala-Ala

L-Alanine β-naphthylamide protease substrate

A2628

L-Alanine β-naphthylamide

form

powder

form

powder

form

powder

form

powder

assay

≥98% (TLC)

assay

≥98% (TLC)

assay

≥99% (TLC)

assay

≥98% (TLC)

storage temp.

−20°C

storage temp.

-

storage temp.

-

storage temp.

2-8°C

Quality Level

200

Quality Level

200

Quality Level

200

Quality Level

200

color

white

color

white

color

white to off-white

color

-

Amino Acid Sequence

Ala-Ala-Ala

Application

Trialanine (Ala-Ala-Ala) may be used along with other short chain alanines, tetra- and penta-alanine, as model compounds to study physicochemical parameters of small peptides.

Storage Class

11 - Combustible Solids

wgk_germany

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

    • Choose from one of the most recent versions:

    Certificates of Analysis (COA)

    Lot/Batch Number
    BCBW9583
    BCBN6172V
    BCBH2496V
    1402028V
    1417331V

    Don't see the Right Version?

    If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

    Search for a COA

    Already Own This Product?

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

    Visit the Document Library

    Customers Also Viewed

    Slide 1 of 3

    1 of 3

    Gly-Gly-Gly BioUltra, ≥99.0% (NT)

    Sigma-Aldrich

    50239

    Gly-Gly-Gly

    Phe-Phe

    Sigma-Aldrich

    P4126

    Phe-Phe

    Poly-DL-alanine mol wt 1,000-5,000

    Sigma-Aldrich

    P9003

    Poly-DL-alanine

    K Karthikeyan et al.
    AAPS PharmSciTech, 13(1), 143-149 (2011-12-15)
    Nonsteroidal anti-inflammatory drugs (NSAIDs) induce gastric injury on long-term usage. This study aims at reducing the side effect of NSAIDs by encapsulating in zein, an acid-resistant biopolymer. Aceclofenac-loaded zein microspheres were prepared by emulsification and solvent evaporation method. The stability
    Kyung Rok Chu et al.
    Archives of pharmacal research, 35(7), 1187-1195 (2012-08-07)
    This study examined the effects of the particle size of various poorly water-soluble drugs on their dissolution behavior through physicochemical and mathematical analysis. As model drugs, hydrochlorothiazide, aceclofenac, ibuprofen and a discovery candidate were selected. The materials were crystallized using
    Erik Legrand
    Expert opinion on pharmacotherapy, 5(6), 1347-1357 (2004-05-28)
    Aceclofenac (Almirall Prodesfarma SA) is an oral NSAID that is effective in the treatment of painful inflammatory diseases and has been used to treat > 75 million patients worldwide. It has proved as effective as diclofenac, naproxen and piroxicam in
    R N Brogden et al.
    Drugs, 52(1), 113-124 (1996-07-01)
    Aceclofenac is a phenylacetic acid derivative with anti-inflammatory and analgesic properties similar to those of diclofenac. However, preclinical studies suggest that the potential of aceclofenac to cause gastrointestinal damage is less than that of diclofenac. Double-blind comparative trials indicate that
    Madhusmruti Khandai et al.
    Current drug delivery, 9(5), 495-505 (2012-04-24)
    The aim of this present research work was to prepare and evaluate alginate microspheres of aceclofenac by ionic gelation method for targeting the drug release in intestinal region and decrease distinct tissue protection in the stomach. This method offers to
    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