Indolelactic acid | CAS:1821-52-9 | Manufacturer ChemFaces

Indolelactic acid

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Size /Price /Stock	10 mM * 1 mL in DMSO / $29.6 / In-stock
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Indolelactic acid Description

Source:	The roots of Heracleum candicans.
Solvent:	Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Storage:	Providing storage is as stated on the product vial and the vial is kept tightly sealed, the product can be stored for up to 24 months(2-8C). Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20C. Generally, these will be useable for up to two weeks. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please email to: service@chemfaces.com
After receiving:	The packaging of the product may have turned upside down during transportation, resulting in the natural compounds adhering to the neck or cap of the vial. take the vial out of its packaging and gently shake to let the compounds fall to the bottom of the vial. for liquid products, centrifuge at 200-500 RPM to gather the liquid at the bottom of the vial. try to avoid loss or contamination during handling.

Recently, ChemFaces products have been cited in many studies from excellent and top scientific journals

More...

Cell. 2018 Jan 11;172(1-2):249-261.e12.
doi: 10.1016/j.cell.2017.12.019.
IF=36.216(2019)

PMID: 29328914

Cell Metab. 2020 Mar 3;31(3):534-548.e5.
doi: 10.1016/j.cmet.2020.01.002.
IF=22.415(2019)

PMID: 32004475

Mol Cell. 2017 Nov 16;68(4):673-685.e6.
doi: 10.1016/j.molcel.2017.10.022.
IF=14.548(2019)

PMID: 29149595

ACS Nano. 2018 Apr 24;12(4): 3385-3396.
doi: 10.1021/acsnano.7b08969.
IF=13.903(2019)

PMID: 29553709

Nature Plants. 2016 Dec 22;3: 16206.
doi: 10.1038/nplants.2016.205.
IF=13.297(2019)

PMID: 28005066

Sci Adv. 2018 Oct 24;4(10): eaat6994.
doi: 10.1126/sciadv.aat6994.
IF=12.804(2019)

PMID: 30417089

Structure Identification:

Biologia Plantarum, 1970, 12(3):246-255.

Pathways of IAA production from tryptophan by plants and by their epiphytic bacteria: Metabolism of indolepyruvic acid and indolelactic acid.[Reference: WebLink]

METHODS AND RESULTS:
Metabolites of indolepyruvic acid and Indolelactic acid were investigated using 2 systems: a bacterial (pea stem homogenates containing the epiphytic bacteria) and a plant system (pea stem sections under sterile conditions). The products of spontaneous indolepyruvic acid decomposition in aqueous solution and during chromatography were investigated, too.Biological indolepyruvic acid conversion yields, besides those substance amounts which occur spontaneously, indoleacetic acid, indoleethanol (tryptophol) and (only in the sterile plant system) indoleacetaldehyde. An inhibitor extract from pea stems decreases the indoleacetic acid and increases the indoleethanol and indoleacetaldehyde gain.
CONCLUSIONS:
Indolelactic acid is not metabolized in the sterile plant sections. Indolelactic acid oxidation by the bacteria-containing homogenate yields indolepyruvic acid and is inhibited by the inhibitor extract.

Journal of Chromatography A, 2015, 205( 1):125-137.

Identification of 3-indoleacetic acid in pinus sylvestris L. by gas chromatography-mas spectrometry, and quantitative analysis by ion-pair reversed-phase liquid chromatography wit spectrofluorimetric detection.[Reference: WebLink]

METHODS AND RESULTS:
The phytochormone 3-indoleacetic acid (IAA) was conclusively identified by gas chromatography-mas spetrometry of its methyl ester in purified extracts of Scots pine, Pinus sylvestris L. Preceding purification included reversed-phase ion-pair chromatography on a Nucleosil C18 column with tetrabutylammonium ion as counter ion. A number of indole acids were separated in this high-performance liquid chromatographic (HPLC) system. In particular, IAA was separated from the reported plant constituents 4-chloro-IAA, 5-hydroxy-IAA, 3-indoleacrylic acid, 3-Indolelactic acid, 3-indolepropionic acid, 3-indolebutyric acid and tytophan. In connection with a spectrofluorine detector, the HPLC system was also used for the quantitative analysis of IAA in pine samples. Systematic errors caused a constant under-estimation of the IAA content by 12% and could easily be corrected for. The random error was 14%. Eight-week-old pine seedings contained 46 ng g−1 of IAA.
CONCLUSIONS:
The sensitivity of the method, applied to the analysis of pine extracts, was 50 pg of IAA. Evidence is presented that the method, when applied to the analysis of pine extracts, is specific of IAA.

CAS No.	1821-52-9	Price	$100 / 20mg
Catalog No.	CFN95263	Purity	>=98%
Molecular Weight	205.2	Type of Compound	Alkaloids
Formula	C₁₁H₁₁NO₃	Physical Description	Powder
Download	COA MSDS	Similar structural	Comparison (Web) (SDF)

Product Name	Indolelactic acid
CAS No.:	1821-52-9
Catalog No.:	CFN95263
Molecular Formula:	C₁₁H₁₁NO₃
Molecular Weight:	205.2 g/mol
Purity:	>=98%
Type of Compound:	Alkaloids
Physical Desc.:	Powder
Source:	The roots of Heracleum candicans.
Solvent:	Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Price:	$100 / 20mg
Download:	COA MSDS
Similar structural:	Comparison (Web) (SDF)

Size /Price /Stock	10 mM * 100 uL in DMSO / Inquiry / In-stock 10 mM * 1 mL in DMSO / Inquiry / In-stock
Related Libraries	Alkaloids Compound Library

	1 mg	5 mg	10 mg	20 mg	25 mg
1 mM	4.8733 mL	24.3665 mL	48.7329 mL	97.4659 mL	121.8324 mL
5 mM	0.9747 mL	4.8733 mL	9.7466 mL	19.4932 mL	24.3665 mL
10 mM	0.4873 mL	2.4366 mL	4.8733 mL	9.7466 mL	12.1832 mL
50 mM	0.0975 mL	0.4873 mL	0.9747 mL	1.9493 mL	2.4366 mL
100 mM	0.0487 mL	0.2437 mL	0.4873 mL	0.9747 mL	1.2183 mL

CFN99899	Indole-3-acrylic acid methyl ester	19626-92-7	201.2	C₁₂H₁₁NO₂
CFN95263	Indolelactic acid	1821-52-9	205.2	C₁₁H₁₁NO₃
CFN97559	Methyl 3-carbazolecarboxylate	97931-41-4	225.2	C₁₄H₁₁NO₂
CFN97256	1H-Indole-3-carboxylic acid	771-50-6	161.2	C₉H₇NO₂
CFN97515	Methyl 3-indolecarboxylate	942-24-5	175.2	C₁₀H₉NO₂
CFN96192	2-(1H-Indole-3-carboxamido)benzoic acid	171817-95-1	280.3	C₁₆H₁₂N₂O₃
CFN91534	Cephalandole B	915315-44-5	294.3	C₁₇H₁₄N₂O₃
CFN96487	Indole-3-glyoxylamide	5548-10-7	188.18	C₁₀H₈N₂O₂
CFN97552	Paniculidine A	97399-93-4	231.3	C₁₄H₁₇NO₂
CFN97553	Paniculidine B	97399-94-5	233.3	C₁₄H₁₉NO₂