C0413
4-Chlorophenoxyacetic acid
BioReagent, suitable for plant cell culture, crystalline
Synonym(s):
4-CPA
Sign In to View Organizational & Contract Pricing.
Select a Size
About This Item
Empirical Formula (Hill Notation):
C8H7ClO3
CAS Number:
Molecular Weight:
186.59
UNSPSC Code:
10171502
NACRES:
NA.72
PubChem Substance ID:
EC Number:
204-581-3
Beilstein/REAXYS Number:
1211804
MDL number:
Form:
crystalline
InChI key
SODPIMGUZLOIPE-UHFFFAOYSA-N
InChI
1S/C8H7ClO3/c9-6-1-3-7(4-2-6)12-5-8(10)11/h1-4H,5H2,(H,10,11)
SMILES string
OC(=O)COc1ccc(Cl)cc1
product line
BioReagent
form
crystalline
technique(s)
cell culture | plant: suitable
application(s)
agriculture
Quality Level
Looking for similar products? Visit Product Comparison Guide
Application
4-Chlorophenoxyacetic acid has been used in para-chlorophenoxyacetic acid (p-CPA) residue assay.
4-chlorophenoxy acetic acid (4-CPA), a chlorine derivative of phenoxyacetic acid (PA), is a plant growth regulator used as a herbicide.
Biochem/physiol Actions
4-Chlorophenoxyacetic acid is a synthetic auxin, that is used to induce parthenocarpic ovary growth on flowers of wild type plants.
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral
Storage Class
11 - Combustible Solids
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Tomato fruit development in the auxin-resistant dgt mutant is induced by pollination but not by auxin treatment
Mignolli F, et al.
Journal of Plant Physiology, 169(12), 1165-1172 (2012)
p-CPA enhances growth and quality of muskmelon fruits
Hayata Y, et al.
Plant Growth Regulation, 36(1), 13-18 (2002)
Ediz Yeşilkaya et al.
Hormone research, 72(4), 225-235 (2009-09-30)
Plant growth regulators are considered to leave minimal amounts of remnants and therefore cause no significant side effects in humans. In this study, we aimed to investigate the hormonal and histopathological effects of 4-chlorophenoxy acetic acid (4-CPA), a commonly used
Oscar Moran et al.
Biochemistry, 42(18), 5176-5185 (2003-05-07)
Molecular simulation techniques were applied to predict the interaction of the CLC-0 Cl(-) channel and the channel-blocking molecule p-chlorophenoxyacetic acid (CPA). A three-dimensional model of the CLC-0 channel was constructed on the basis of the homology with the bacterial Cl(-)
Alessio Accardi et al.
The Journal of general physiology, 122(3), 277-293 (2003-08-13)
The Torpedo Cl- channel, CLC-0, is inhibited by clofibric acid derivatives from the intracellular side. We used the slow gate-deficient mutant CLC-0C212S to investigate the mechanism of block by the clofibric acid-derivative p-chlorophenoxy-acetic acid (CPA). CPA blocks open channels with
Related Content
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service