Home - Products - Others - Other Targets - Indole-3-acetic acid

Indole-3-acetic acid

CAS No. 87-51-4

Indole-3-acetic acid( Indoleacetic acid | Heteroauxin | Hexteroauxin | Rhizopin )

Catalog No. M19209 CAS No. 87-51-4

Indole-3-acetic acid (IAA) is the most common plant hormone of the auxin class and it regulates various aspects of plant growth and development.

Purity : >98% (HPLC)

COA

Datasheet

HNMR

HPLC

MSDS

Handing Instructions

Size	Price / USD	Stock	Quantity
500MG	37	In Stock
1G	Get Quote	In Stock

Get Quotation Bulk Inquiry Add to Cart

Biological Information

Product Name

Indole-3-acetic acid
Note

Research use only, not for human use.
Brief Description

Indole-3-acetic acid (IAA) is the most common plant hormone of the auxin class and it regulates various aspects of plant growth and development.
Description

Indoleacetic acid is used to apply as a plant growth hormone. It is an inducer of plant cell elongation and division shown to cause uncontrolled growth.
In Vitro

——
In Vivo

——
Synonyms

Indoleacetic acid | Heteroauxin | Hexteroauxin | Rhizopin
Pathway

Others
Target

Other Targets
Recptor

Others
Research Area

——
Indication

——

Chemical Information

CAS Number

87-51-4
Formula Weight

175.18
Molecular Formula

C10H9NO2
Purity

>98% (HPLC)
Solubility

DMSO : ≥ 30 mg/mL; 171.25 mM
SMILES

C1=CC=C2C(=C1)C(=CN2)CC(=O)O
Chemical Name

1H-Indole-3-acetic acid

Shipping & Storage Information

Storage

(-20℃)
Shipping

With Ice Pack
Stability

≥ 2 years

Reference

Calculator

Molecular Weight Calculator

Dilution Calculator

Molarity Calculator

molnova catalog

related products

pTH (53-84) (human)

pTH (53-84) (human)
BDC2.5 mimotope 1040...

BDC2.5 mimotope 1040-51 is a mimotope peptide for diabetogenic T cell clone BDC2.5. isolated from non-obese diabetic mice.This is a effectively agonistic peptide (mimotope) for diabetogenic T cell clone BDC2.5. from non-obese diabetic (NOD) mice. T cells from prediabetic and diabetic NODs respond to BDC2.5 mimotope peptides.
Ralinepag

Ralinepag is a potent, orally bioavailable and non-prostanoid prostacyclin (IP) receptor agonist, with EC50s of 8.5 nM, 530 nM and 850 nM for human and rat IP receptor and human DP1 receptor, respectively.

Sign In Join Free