2,4-D is 2,4-dichlorophenoxyacetic acid, a synthetic auxin with molecular formula . The 2 and 4 specify positions of chlorine substituents on the aromatic ring. The acid name identifies a particular chemical structure, rather than every compound that produces an auxin-like response.[ref]
PubChem Compound database by National Center for Biotechnology Information. CID1486, structure, formula and synthetic-auxin classification
Its transport behavior makes it informative in comparisons with indole-3-acetic acid and naphthaleneacetic acid. A 2001 Arabidopsis thaliana experiment compared an AUX1-defective mutant under matched external auxin treatments. In the reported gravitropism assay, the membrane-permeable analogue naphthaleneacetic acid restored the response, whereas the corresponding 2,4-D treatment did not.[ref]
That contrast concerns a particular transport defect and endpoint. Equal external concentrations do not establish equal concentrations within the responsive cells, and a missing response does not by itself show that a compound lacks hormonal activity. Chemical uptake, subsequent distribution and the measured growth response are separate parts of the mechanism.
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