Skip to Content
Merck
All Photos(1)

Documents

Safety Information

345911

Sigma-Aldrich

N-(3-Indolylacetyl)-L-alanine

98%

Synonym(s):

IAA-L-Ala, Indole-3-acetyl-L-alanine

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

About This Item

Empirical Formula (Hill Notation):
C13H14N2O3
CAS Number:
57105-39-2
Molecular Weight:
246.26
MDL number:
MFCD00050395
UNSPSC Code:
12352209
eCl@ss:
32160406
PubChem Substance ID:
24861360
NACRES:
NA.22

Assay

98%

form

solid

optical activity

[α]24/D −21°, c = 1 in methanol

reaction suitability

reaction type: solution phase peptide synthesis

mp

138-140 °C (lit.)

application(s)

peptide synthesis

SMILES string

C[C@H](NC(=O)Cc1c[nH]c2ccccc12)C(O)=O

InChI

1S/C13H14N2O3/c1-8(13(17)18)15-12(16)6-9-7-14-11-5-3-2-4-10(9)11/h2-5,7-8,14H,6H2,1H3,(H,15,16)(H,17,18)/t8-/m0/s1

InChI key

FBDCJLXTUCMFLF-QMMMGPOBSA-N

Looking for similar products? Visit Product Comparison Guide

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

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

345911-1G:
345911-BULK:
345911-250MG:
345911-VAR:

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

Miguel A Uc-Chuc et al.
International journal of molecular sciences, 21(13) (2020-07-09)
Despite the existence of considerable research on somatic embryogenesis (SE), the molecular mechanism that regulates the biosynthesis of auxins during the SE induction process remains unknown. Indole-3-acetic acid (IAA) is an auxin that is synthesized in plants through five pathways.
João Daniel Santos Fernandes et al.
PloS one, 10(7), e0132369-e0132369 (2015-07-15)
Metabolic diversity is an important factor during microbial adaptation to different environments. Among metabolic processes, amino acid biosynthesis has been demonstrated to be relevant for survival for many microbial pathogens, whereas the association between pathogenesis and amino acid uptake and

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