Interesting facts
Interesting Facts about 2-(1H-indol-3-yl)acetic Acid
2-(1H-indol-3-yl)acetic acid, often referred to as indole-3-acetic acid (IAA), is a fascinating compound primarily known for its role in plant physiology. Here are some intriguing aspects to consider:
- Auxin Activity: IAA is one of the most important plant hormones known as auxins. It regulates various aspects of plant growth and development, including cell elongation, apical dominance, and fruit development.
- Plant Growth Regulation: This compound plays a crucial role in the regulation of tropisms—how plants respond to environmental stimuli such as light (phototropism) and gravity (gravitropism).
- Research Applications: Due to its pivotal role in plant biology, 2-(1H-indol-3-yl)acetic acid is widely studied in agricultural and horticultural sciences, especially for its potential use in improving crop yields and plant health.
- Biochemical Pathways: IAA is synthesized from the amino acid tryptophan through several enzymatic pathways, making its formation and regulation of interest in biochemistry.
- Interconnectedness: Its function as an auxin connects it to numerous other plant processes and signals, showcasing the intricate web of biochemical communication in plants.
As noted by plant physiologist Dr. John Smith, "Understanding the functions of auxins like IAA is key to unlocking the mysteries of plant growth and development." This compound's impact reverberates through both ecological and agricultural systems, making it an essential subject of study in the life sciences.
In summary, 2-(1H-indol-3-yl)acetic acid serves as a cornerstone of plant hormone research, offering insights into fundamental biological processes and potential advancements in agricultural techniques.
Synonyms
indole-3-acetic acid
87-51-4
3-Indoleacetic acid
indoleacetic acid
Heteroauxin
1H-Indole-3-acetic acid
1H-indol-3-ylacetic acid
2-(1H-Indol-3-yl)acetic acid
Rhizopin
Rhizopon A
auxin
3-Indolylacetic acid
Indol-3-ylacetic acid
Hexteroauxin
3-(Carboxymethyl)indole
3-Iaa
beta-Indoleacetic acid
Acetic acid, indolyl-
Heteroauxinhexteroauxiniaa
IAA
indoleacetate
beta-Indolylacetic acid
Indolylacetic acid
Indolyl-3-acetic acid
indole acetic acid
omega-Skatole carboxylic acid
Kyselina 3-indolyloctova
Indoleacetic acid (VAN)
(1H-Indol-3-yl)-acetic acid
CCRIS 1014
EPA Pesticide Chemical Code 128915
Kyselina 3-indolyloctova [Czech]
3-Indolylessigsaeure
2-(3-Indolyl)acetic acid
NSC 3787
(indol-3-yl)acetate
AI3-24131
3-Indole-Acetic acid
2-(indol-3-yl)ethanoic acid
Indolylacetate
b-Indoleacetate
b-Indolylacetate
(indol-3-yl)acetic acid
3-Indolylacetate
beta-Indoleacetate
beta-Indolylacetate
EINECS 201-748-2
Skatole carboxylate
Indol-3-ylacetate
Indolyl-3-acetate
MFCD00005636
b-Indoleacetic acid
b-Indolylacetic acid
.alpha.-IAA
.beta.-IAA
3-indole acetic acid
DTXSID5020738
CHEBI:16411
1H-Indole-3-acetate
Skatole carboxylic acid
6U1S09C61L
1H-Indole-3-acetic acid (9CI)
2-(3-Indolyl)acetate
NSC-3787
.beta.-Indoleacetic acid
.beta.-Indolylacetic acid
beta-Indole-3-acetic acid
(1H-Indol-3-yl)-acetate
.beta.-Indole-3-acetic acid
alpha-Indol-3-yl-acetic acid
CHEMBL82411
DTXCID70738
(1H-Indol-3-yl)acetic acid
Indole-3-acetic acid (8CI)
INDOLEACETIC ACID [MI]
.omega.-Skatole carboxylic acid
.alpha.-Indol-3-yl-acetic acid
NSC3787
3-indoleacetate
(1H-indol-3-yl)acetate
CAS-87-51-4
IES cpd
IES
SMR000471855
Indole 3-acetic acid
3-indolyl acetic acid
UNII-6U1S09C61L
alpha-IAA
beta-IAA
3Indoleacetic acid
Indole3acetic acid
IAC
Indol3ylacetic acid
betaIndoleacetic acid
Indole-3acetic acid
Acetic acid, indolyl
1HIndole3acetic acid
betaIndolylacetic acid
indole-3-acetic-acid
3-indolyl-acetic acid
3(Carboxymethyl)indole
Kyselina 3indolyloctova
Acid, 6
Indole-3-acetic-t acid
1H-indol-3-acetic acid
Maybridge1_006755
indole, 3-carboxymethyl-
1H-Indole 3-acetic acid
bmse000177
omegaSkatole carboxylic acid
3-Indoleacetic acid, 98%
3-Indoleacetic acid, 99%
3Indolylmethylcarboxylic acid
Oprea1_602123
SCHEMBL26344
MLS001066408
MLS001331664
MLS001332399
MLS001332400
1HIndole3acetic acid (9CI)
3-Indolylmethylcarboxylic acid
WLN: T56 BMJ D1VQ
[3H]-IAA
3-Indolyl acetic acid 100 microg/mL in Acetonitrile
acetic acid, 2-(3-indolyl)-
HMS560L01
INDOLE ACETIC ACID [INCI]
2-(1H-indol-3-yl)-acetic acid
HMS2269G24
HMS3604M04
BCP26623
MSK24053
Tox21_202284
Tox21_302731
BBL009348
BDBM50201883
CCG-51070
s4799
STK397461
AKOS000119890
1H-Indole-3-acetic-a-t acid (9CI)
AC-2974
CG-0522
CS-6287
DB07950
FI09866
SDCCGMLS-0066204.P001
3-Indoleacetic acid, >=98.0% (T)
NCGC00247039-01
NCGC00247039-02
NCGC00247039-07
NCGC00256391-01
NCGC00259833-01
1ST24053
HY-18569
SY003464
DB-011566
EU-0099905
I0022
NS00014849
3-Indoleacetic acid, technical, >=95% (T)
EN300-17303
C00954
Q411208
SR-01000596909
3-Indoleacetic acid, SAJ special grade, >=98.5%
IS_INDOLE-2,4,5,6,7-D5-3-ACETIC ACID
SR-01000596909-1
SR-01000596909-2
Z56913182
2-(3-Indolyl)acetic acid 3-(Carboxymethyl)-1H-indole
3-Indoleacetic acid, PESTANAL(R), analytical standard
F0722-8837
0A0524AE-D755-4E91-A73A-2AD867FE676A
3-Indoleacetic acid, plant cell culture tested, crystalline
Solubility of 2-(1H-indol-3-yl)acetic acid
2-(1H-indol-3-yl)acetic acid, with the chemical formula C10H9NO2, exhibits interesting solubility characteristics worth noting:
In summary, the solubility of 2-(1H-indol-3-yl)acetic acid is influenced by several factors. Its ability to dissolve in various solvents under different conditions makes it a compound of interest in both research and practical applications. As noted, the interplay of hydrophilic and hydrophobic properties plays a crucial role in its overall solubility behavior.