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I5508

Sigma-Aldrich

DL-Indole-3-lactic acid

99%

Synonym(s):

β-(3-Indolyl)lactic acid, 2-Hydroxy-3-(3-indolyl)propanoic acid, 3-(3-Indolyl)-2-hydroxypropanoic acid, 3-Indolyllactic acid, Indolelactic acid

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About This Item

Empirical Formula (Hill Notation):
C11H11NO3
CAS Number:
832-97-3
Molecular Weight:
205.21
EC Number:
212-627-9
MDL number:
MFCD00005642
UNSPSC Code:
12352100
PubChem Substance ID:
24896071
NACRES:
NA.22

Quality Level

200

Assay

99%

mp

145-146 °C (lit.)

SMILES string

OC(Cc1c[nH]c2ccccc12)C(O)=O

InChI

1S/C11H11NO3/c13-10(11(14)15)5-7-6-12-9-4-2-1-3-8(7)9/h1-4,6,10,12-13H,5H2,(H,14,15)

InChI key

XGILAAMKEQUXLS-UHFFFAOYSA-N

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General description

DL-Indole-3-lactic acid can serve as a building block in the synthesis of various molecules, like Indole-3-acetic acid (IAA)

Application

Reactant for preparation of:
  • Antibacterial agents
  • Dietary sweetener

Packaging

Bottomless glass bottle. Contents are inside inserted fused cone.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

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’.

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Beneficial effects elicited by the root endophyte Piriformospora indica are widely known, but the mechanism by which these are achieved is still unclear. It is proposed that phytohormones produced by the fungal symbiont play a crucial role in the interaction
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Journal of proteome research, 9(8), 4176-4188 (2010-06-15)
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Determination of urinary 5-hydroxyindole-3-acetic acid using solid-phase extraction and reversed-phase high-performance liquid chromatography with electrochemical detection.
P P Chou et al.
Journal of chromatography, 341(1), 167-171 (1985-05-31)
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