3-Indoleacetic acid - for plant cell culture, ≥98% , CAS No.87-51-4

CAS: 87-51-4 Cat. No.: I101074 Molecular Weight: 175.18 Beilstein Registry Number: 143358 EC Number: 201-748-2
AVAILABLE TO ORDER
GRADE & PURITY Suitable for plant cell culture ? Plant cell-culture grade — formulated for plant tissue and cell cultures. Use in plant biotechnology, callus, and suspension culture work. ≥98%
Synonyms
.beta.-Indoleacetic acid | bmse000177 | 1H-indol-3-ylacetic acid | Tox21_302731 | MLS001331664 | .beta.-IAA | auxin | b-Indolylacetic acid | MLS001332400 | (1H-indol-3-yl)acetate | (1H-Indol-3-yl)-acetate | .alpha.-IAA | 3-Indolylacetic acid | 3-indolyl-a
Storage
Store at -20°C,Argon charged
Shipped In
Ice chest + Ice pads
 ·  off list, applied to all prices below.
Size
Status
Price
Qty
5g
I101074-5g
1

$55.90

$65.90
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25g
I101074-25g
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100g
I101074-100g
3

$704.90

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Why this grade

for plant cell culture, ≥98% Suitable for plant cell culture for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Store at -20°C,Argon charged Ships Ice chest + Ice pads Check lot-specific COA for exact specifications.

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Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

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Literature proof

Cited in 35 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Synonyms
.beta.-Indoleacetic acid | bmse000177 | 1H-indol-3-ylacetic acid | Tox21_302731 | MLS001331664 | .beta.-IAA | auxin | b-Indolylacetic acid | MLS001332400 | (1H-indol-3-yl)acetate | (1H-Indol-3-yl)-acetate | .alpha.-IAA | 3-Indolylacetic acid | 3-indolyl-a
Specifications & Purity
for plant cell culture, ≥98%
Storage
Store at -20°C, Argon charged
Shipped In
Ice chest + Ice pads
This product requires cold chain shipping. Ground and other economy services are not available.
Grade
Suitable for plant cell culture
Purity
≥98%
Names and Identifiers
Pubchem Sid504750420
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504750420
Canonical SmilesC1=CC=C2C(=C1)C(=CN2)CC(=O)O
IUPAC Name2-(1H-indol-3-yl)acetic acid
InChIKeySEOVTRFCIGRIMH-UHFFFAOYSA-N
INCHI1S/C10H9NO2/c12-10(13)5-7-6-11-9-4-2-1-3-8(7)9/h1-4,6,11H,5H2,(H,12,13)
Isomeric SMILES C1=CC=C2C(=C1)C(=CN2)CC(=O)O
WGK Germany 3
RTECS NL3150000
Molecular Weight 175.18
Beilstein 143358
Reaxy-Rn 143358
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=143358&ln=

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganoheterocyclic compounds
ClassIndoles and derivatives
SubclassIndolyl carboxylic acids and derivatives
Intermediate Tree Nodes Not available
Direct ParentIndole-3-acetic acid derivatives
Alternative Parents 3-alkylindoles  Substituted pyrroles  Benzenoids  Heteroaromatic compounds  Monocarboxylic acids and derivatives  Carboxylic acids  Azacyclic compounds  Organopnictogen compounds  Organonitrogen compounds  Organic oxides  Hydrocarbon derivatives  Carbonyl compounds  
Molecular FrameworkAromatic heteropolycyclic compounds
Substituents Indole-3-acetic acid derivative - 3-alkylindole - Indole - Substituted pyrrole - Benzenoid - Heteroaromatic compound - Pyrrole - Azacycle - Monocarboxylic acid or derivatives - Carboxylic acid - Carboxylic acid derivative - Carbonyl group - Organopnictogen compound - Organooxygen compound - Organonitrogen compound - Organic oxygen compound - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Aromatic heteropolycyclic compound
DescriptionThis compound belongs to the class of organic compounds known as indole-3-acetic acid derivatives. These are compounds containing an acetic acid (or a derivative) linked to the C3 carbon atom of an indole.
External Descriptors Indole alkaloids - Auxins
3D Structure
Interactive Chemical Structure Model





Associated Targets(Human)
ACHE Tclin Acetylcholinesterase (18204 Activities)
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PDF Tchem Peptide deformylase mitochondrial (169 Activities)
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ALB Tchem Serum albumin (2651 Activities)
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KYAT1 Tbio Kynurenine--oxoglutarate transaminase I (96 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
FLT3 Tclin Tyrosine-protein kinase receptor FLT3 (13481 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Liver microsomes (16955 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Associated Targets(non-human)
def Peptide deformylase (54 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Escherichia coli (133304 Activities)
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Bacillus subtilis (32866 Activities)
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Oryza sativa (2923 Activities)
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Saccharomyces cerevisiae (19171 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
V79 (1637 Activities)
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Lactuca sativa (1092 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
BCHE Cholinesterase (8742 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Avena sativa (212 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Cucumis sativus (803 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Fusarium culmorum (260 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Macrophomina phaseolina (474 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Rhizoctonia solani (2251 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ftmPT1 Brevianamide F prenyltransferase (40 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PDF1A Peptide deformylase 1A, chloroplastic (24 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Globisporangium debaryanum (107 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
clpP ATP-dependent Clp protease proteolytic subunit (245 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Laetisaria fuciformis (2 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Cryphonectria parasitica (24 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Fuchsia (11 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Vigna mungo (68 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mechanisms of Action
Certificates(CoA,COO,BSE/TSE and Analysis Chart)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

13 results found

Lot NumberCertificate TypeDateItem
G2222432Certificate of AnalysisMay 09, 2026 I101074
G2222459Certificate of AnalysisMay 09, 2026 I101074
C2630021Certificate of AnalysisApr 07, 2026 I101074
H2511748Certificate of AnalysisAug 14, 2025 I101074
E2013102Certificate of AnalysisMar 14, 2024 I101074
F2009084Certificate of AnalysisMar 06, 2024 I101074
J2317022Certificate of AnalysisOct 19, 2023 I101074
D2419066Certificate of AnalysisJul 05, 2022 I101074
F2506086Certificate of AnalysisJul 05, 2022 I101074
G2222439Certificate of AnalysisJul 05, 2022 I101074
H2409091Certificate of AnalysisJul 05, 2022 I101074
H2525099Certificate of AnalysisJul 05, 2022 I101074
L2431092Certificate of AnalysisJul 05, 2022 I101074

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Chemical and Physical Properties
SensitivityAir and light sensitive
Flash Point(°F)339.8℉
Flash Point(°C)171℃
Melt Point(°C)167°C
Molecular Weight175.180 g/mol
XLogP31.400
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count2
Rotatable Bond Count2
Exact Mass175.063 Da
Monoisotopic Mass175.063 Da
Topological Polar Surface Area53.100 Ų
Heavy Atom Count13
Formal Charge0
Complexity205.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Documents & Articles
Citations of This Product
References
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15. Cheng Ye, Tian Dong-Yang, Chen Cui-Li, Bao Ning, Wu Zeng-Qiang.  (2024)  Determination of indole-3-acetic acid using disposable molecularly imprinted electrochemical sensors based on bifunctional monomers.  MICROCHIMICA ACTA,  191  (10): (1-9).  [PMID:39327334] [10.1007/s00604-024-06717-2]
16. Juan Liu, Shiqing Sun, Kangyu Chen, Shumei Gao, Dixing Chen, Yuejin Zhang, Changwei Hu.  (2025)  Discerning promotion mechanisms of fungi Clonostachys rosea on growth of freshwater microalga Chlorella sp. by non-contact culture.  Algal Research-Biomass Biofuels and Bioproducts,      [PMID:] [10.1016/j.algal.2025.103967]
17. Zhenhui Li, Song Lin, Mei Zhu, Xiaoman Liu, Xin Huang.  (2025)  Enhanced Antibacterial Activity of Hydrophobic Modified Lysozyme Against Gram-Negative Bacteria Without Accumulated Resistance.  MOLECULES,  30  (2): (232).  [PMID:39860102] [10.3390/molecules30020232]
18. Xin Tan, Renwang Sheng, Weikun Li, Yinghua Tao, Zonghao Liu, Ning Yang, Syeda Safia Hashmi, Feiling Feng, Fangzhou Liu, Liqin Ge.  (2025)  Mannose-Glycated Metal-Phenolic Microcapsules Orchestrate Phenotype Switch of Macrophages for Boosting Tumor Immunotherapy.  Advanced Science,      [PMID:40014038] [10.1002/advs.202415565]
19. Zheng Jianxiu, Wang Liyan, Liu Ahui, Shen Haofei, Wang Bin, Jiang Yanbiao, Jing Panpan, Guan Defeng, Yu Liulin, Zhang Xuehong.  (2024)  Predicting the therapeutic role and potential mechanisms of Indole-3-acetic acid in diminished ovarian reserve based on network pharmacology and molecular docking.  HEREDITAS,  161  (1): (1-17).  [PMID:39568012] [10.1186/s41065-024-00348-6]
20. Yi Hao, Jian Shang, Shuyan Liu, Xuemeng Tian, Xin Yao, Fengjun Liu, Ruizhen Zhu, Yue Wang, Ruixia Gao, Sicen Wang.  (2025)  Preparation of protein-resistant magnetic molecularly imprinted polymers as solid-phase extraction adsorbents via a one-stone-two-birds strategy for selective enrichment of tetracycline in milk.  TALANTA,      [PMID:39904252] [10.1016/j.talanta.2025.127678]
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22. Lisi Wang, Xiaoqing Li, Yijing Ai, Brij Mohan, Hongji Li, Zhisong Lu, Baoli Wang, Wei Sun.  (2025)  Sustainable Precursor-Based Titanium Dioxide–Graphene Nanocomposite Electrochemical Sensor for Sensitive Detection of Diuron in Vegetables.  Foods,  14  (17): (2946).  [PMID:40941062] [10.3390/foods14172946]
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