EU/US Properties Organoleptics Cosmetics Suppliers Safety Safety in use Safety references References Other Blenders Uses Occurrence Synonyms Articles Notes
 

3-indole butyric acid
butyric acid, indol-3-yl-

Supplier Sponsors

CAS Number: 133-32-4Picture of molecule3D/inchi
Other(deleted CASRN):111150-79-9
ECHA EINECS - REACH Pre-Reg:205-101-5
FDA UNII: 061SKE27JP
Nikkaji Web:J2.525I
Beilstein Number:0171120
MDL:MFCD00005664
XlogP3:2.30 (est)
Molecular Weight:203.24101000
Formula:C12 H13 N O2
BioActivity Summary:listing
NMR Predictor:Predict (works with chrome, Edge or firefox)
Category:pharmaceuticals / chemical synthisis
 
US / EU / FDA / JECFA / FEMA / FLAVIS / Scholar / Patent Information:
Google Scholar:Search
Google Books:Search
Google Scholar: with word "volatile"Search
Google Scholar: with word "flavor"Search
Google Scholar: with word "odor"Search
Google Patents:Search
US Patents:Search
EU Patents:Search
Pubchem Patents:Search
PubMed:Search
NCBI:Search
 
Physical Properties:
Assay: 95.00 to 100.00
Food Chemicals Codex Listed: No
Melting Point: 124.50 °C. @ 760.00 mm Hg
Boiling Point: 426.56 °C. @ 760.00 mm Hg (est)
Vapor Pressure:1.800000 mmHg (est)
Flash Point: 413.00 °F. TCC ( 211.80 °C. ) (est)
logP (o/w): 2.300
Soluble in:
 water, 250 mg/L @ 20 °C (exp)
 water, 1136 mg/L @ 25 °C (est)
 
Organoleptic Properties:
Odor and/or flavor descriptions from others (if found).
 
Cosmetic Information:
None found
 
Suppliers:
Alfa Biotechnology
For experimental / research use only.
3-Indolebutyric acid 98%
BOC Sciences
For experimental / research use only.
3-Indolebutyric acid (IBA) >98%
Odor: characteristic
Use: 3-Indolebutyric acid(IBA) is a plant hormone in the auxin family and is an ingredient in many commercial plant rooting horticultural products.
BST Tianjin Co.
Indole-3-butyric acid
Carbosynth
For experimental / research use only.
Indole-3-butyric acid
Glentham Life Sciences
Indole-3-butyric acid
Penta International
3-INDOLE BUTYRIC ACID
Santa Cruz Biotechnology
For experimental / research use only.
3-Indolebutyric Acid
Sigma-Aldrich: Sigma
For experimental / research use only.
Indole-3-butyric acid ≥99.0% (T)
sds
TCI AMERICA
For experimental / research use only.
3-Indolebutyric Acid >98.0%(HPLC)(T)
sds
 
Safety Information:
Preferred SDS: View
 
Hazards identification
 
Classification of the substance or mixture
GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)
None found.
GHS Label elements, including precautionary statements
 
Pictogram
 
Hazard statement(s)
None found.
Precautionary statement(s)
None found.
Oral/Parenteral Toxicity:
intraperitoneal-mouse LD50 100 mg/kg
"Agrochemicals Handbook," with updates, Hartley, D., and H. Kidd, eds., Nottingham, Royal Soc of Chemistry, 1983-86Vol. A231, Pg. 1983

oral-mouse LD50 100 mg/kg
"Agricultural Chemicals," Thomson, W.T., 4 vols., Fresno, CA, Thomson Publications, 1976/77 revisionVol. 3, Pg. 76, 1976/1977.

oral-rat LD > 500 mg/kg
National Academy of Sciences, National Research Council, Chemical-Biological Coordination Center, Review. Vol. 5, Pg. 7, 1953.

Dermal Toxicity:
Not determined
Inhalation Toxicity:
Not determined
 
Safety in Use Information:
Category:
pharmaceuticals / chemical synthisis
Recommendation for 3-indole butyric acid usage levels up to:
 not for fragrance use.
 
Recommendation for 3-indole butyric acid flavor usage levels up to:
 not for flavor use.
 
Safety References:
European Food Safety Authority (EFSA) reference(s):

Reasoned opinion on the review of the existing maximum residue levels (MRLs) for indolylbutyric acid according to Article 12 of Regulation (EC) No 396/2005
View page or View pdf

EPI System: View
Chemical Carcinogenesis Research Information System:Search
AIDS Citations:Search
Cancer Citations:Search
Toxicology Citations:Search
EPA Substance Registry Services (TSCA):133-32-4
EPA ACToR:Toxicology Data
EPA Substance Registry Services (SRS):Registry
Laboratory Chemical Safety Summary :8617
National Institute of Allergy and Infectious Diseases:Data
WGK Germany:3
4-(1H-indol-3-yl)butanoic acid
Chemidplus:0000133324
RTECS:NL5250000 for cas# 133-32-4
 
References:
 4-(1H-indol-3-yl)butanoic acid
NIST Chemistry WebBook:Search Inchi
Canada Domestic Sub. List:133-32-4
Pubchem (cid):8617
Pubchem (sid):134974585
 
Other Information:
(IUPAC):Atomic Weights of the Elements 2011 (pdf)
Videos:The Periodic Table of Videos
tgsc:Atomic Weights use for this web site
(IUPAC):Periodic Table of the Elements
CHEBI:View
CHEMBL:View
Golm Metabolome Database:Search
KEGG (GenomeNet):C11284
HMDB (The Human Metabolome Database):HMDB02096
FooDB:FDB001404
Export Tariff Code:2933.99.8210
VCF-Online:VCF Volatile Compounds in Food
ChemSpider:View
Wikipedia:View
Formulations/Preparations:
•trade names: hormodin, seradix •technical grade: 97.0%. dust: 0.01%-4.5%; soluble concentrateliquid: 0.0004%-1.03%; wettable powderdust: 0.1%-0.8%. •mixtures: boll-set (+gibberellic acid), cytoplex hms (+gibberellic acid+kinetin), early harvest (+cytokinins+gibberellic acid), maxon ii (+gibberellic acid), pgr-iv (+gibberellic acid), super lagniappe (+cytokinins+gibberellic acid). •trade names: synergol, chryzoplus, chryzopon, chryzosan, chryzotek, chryzotop, rhizopon aa. •discontinued names: rootone.
 
Potential Blenders and core components note
None Found
 
Potential Uses:
None Found
 
Occurrence (nature, food, other):note
 corn leaf
Search Trop Picture
 corn seed
Search Trop Picture
 pea
Search Trop Picture
 potato
Search Trop Picture
 
Synonyms:
 butyric acid, indol-3-yl-
 hormex
 hormodin
 indol-3-butyric acid
4-(1H-indol-3-yl)-butyric acid
4-(1H-indol-3-yl)butanoic acid
4-(indol-3-yl)butyric acid
4-(1H-indol-3-yl)butyric acid
4-indol-3-ylbutanoic acid
4-indol-3-ylbutyric acid
 indol-3,4'-yl butyric acid
 indole 3-butyric acid
 indole-3 butyric acid
 indole-3-butanoic acid
1H-indole-3-butanoic acid
 indole-3-butrylic acid
 indole-3-butyic acid
 indole-3-butyric acid
4-(3-indole)-butyric acid
3-indolebutyric acid
b-indolebutyric acid
3-indolebutyricacid
 indolyl-3-butyric acid
4-(3-indolyl)butanoic acid
4-(3-indolyl)butyric acid
[3-(3-indolyl)propyl]carboxylic acid
3-iodolebutyric acid
 jiffy grow
 oxyberon
 rhizopon AA
 seradix
 stim-root
 

Articles:

PubMed:In vitro regeneration in olive (Olea europaea L.) cv, 'Frontio' from nodal segments.
PubMed:Antioxidant activity of selected stilbenoids and their bioproduction in hairy root cultures of muscadine grape (Vitis rotundifolia Michx.).
PubMed:A comparative study of the removal of 3-indolebutyric acid using advanced oxidation processes.
PubMed:In vitro regeneration through organogenesis and somatic embryogenesis in pigeon pea [ Cajanus cajan (L.) Millsp.] cv. JKR105.
PubMed:Production of lignans in calluses of Schisandra chinensis.
PubMed:Cytokinin induced shoot regeneration and flowering of Scoparia dulcis L. (Scrophulariaceae)-an ethnomedicinal herb.
PubMed:Development of sample preparation method for auxin analysis in plants by vacuum microwave-assisted extraction combined with molecularly imprinted clean-up procedure.
PubMed:Advanced oxidation and mineralization of 3-indole butyric acid (IBA) by Fenton and Fenton-like processes.
PubMed:Extraction and high performance liquid chromatographic determination of 3-indole butyric acid in pea plants by using imidazolium-based ionic liquids as extractant.
PubMed:Synthesis and biological activities of 4-trifluoromethylindole-3-acetic acid: a new fluorinated indole auxin.
PubMed:Determination of household chemicals using gas chromatography and liquid chromatography with tandem mass spectrometry.
PubMed:Expression of NAC1 up-stream regulatory region and its relationship to the lateral root initiation induced by gibberellins and auxins.
PubMed:Plant regeneration from protoplasts isolated from embryogenic suspension cultured cells of Cinnamomum camphora L.
PubMed:Influence of genotype and explant source on indirect organogenesis by in vitro culture of leaves of Melia azedarach L.
PubMed:Auxins affected ginsenoside production and growth of hairy roots in Panax hybrid.
PubMed:Histological analysis of indirect somatic embryogenesis in the Marsh clubmoss Lycopodiella inundata (L.) Holub (Pteridophytes).
PubMed:Somatic embryogenesis and plant recovery from mature tissues of olive cultivars (Olea europaea L.) "canino" and "moraiolo".
PubMed:Transformation of passionfruit (Passiflora edulis fv flavicarpa Degener.) using Agrobacterium tumefaciens.
PubMed:Micropropagation of Morus laevigata Wall. from mature trees.
PubMed:Flavonoid Accumulation Is Correlated with Adventitious Roots Formation in Eucalyptus gunnii Hook Micropropagated through Axillary Bud Stimulation.
PubMed:The influence of auxins, light and cell differentiation on solasodine production bySolanum eleagnifolium Cav. calli.
PubMed:Micropropagation of Stevia rebaudiana Through Leaf Explants from Adult Plants.
PubMed:Gas chromatography-mass spectrometry evidence for several endogenous auxins in pea seedling organs.
PubMed:Comparison of three reagents for detecting indole production by anaerobic bacteria in microtest systems.
 
Notes:
Indole-3-butyric acid (IBA) is a plant hormone in the auxin family and is an ingredient in many commercial plant rooting horticultural products. (Wikipedia)
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