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PACLOBUTRAZOL | ||
PRODUCT IDENTIFICATION | ||
CAS NO |
76738-62-0 |
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EINECS NO. | 266-325-7 | |
FORMULA | C15H20ClN3O | |
MOL WT. | 293.80 | |
H.S. CODE |
2933.99.7900 | |
TOXICITY |
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SYNONYMS | Pestanal; Bonsai; Cultar; Paclobutrazol; | |
[(±)-(R',R')-beta-[(4-Chlorophenyl)methyl]-alpha-(1,1-dimethylethyl)-1H-1,2,4-triazole-1- ethanol; (RS,3RS)-1-(4-Chlorophenyl)-4,4-dimethyl-2-(1H-1,2,4-triazol-1-yl)pentan-3-ol; (2RS,3RS)-1-(4-Chlorophenyl)-4,4-dimethyl-2-(1H-1,2,4-triazol-1-yl)pentan-3-ol; Parlay; Trimmit; beta-((4-Chlorophenyl)methyl)-alpha-(1,1-dimethylethyl)-1H- 1,2,4-triazole-1-ethanol; Other RN: 66346-04-1, 77108-06-6 | ||
SMILES | n1c[n@]([C@@H]([C@H](C(C)(C)C)O)Cc2ccc(cc2)Cl)nc1.n1c[n@](nc1) [C@H]([C@@H](C(C)(C)C)O)Cc1ccc(cc1)Cl | |
CLASSIFICATION |
Plant Growth regulator, Herbicide | |
EXTRA NOTES |
EPA Pesticide Chemical Code 125601 | |
PHYSICAL AND CHEMICAL PROPERTIES | ||
PHYSICAL STATE | white crystals | |
MELTING POINT | 164 - 168 C | |
BOILING POINT |
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SPECIFIC GRAVITY |
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SOLUBILITY IN WATER | Soluble | |
SOLVENT SOLUBILITY |
Soluble in acetone | |
pH | ||
VAPOR DENSITY |
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REFRACTIVE INDEX |
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AUTOIGNITION |
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NFPA RATINGS | ||
FLASH POINT |
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STABILITY | Stable under ordinary conditions. | |
EXTERNAL LINKS & GENERAL DESCRIPTION | ||
Wikipedia Linking - Paclobutrazol Google Scholar Search - Paclobutrazol Drug Information Portal (U.S. National Library of Medicine) - Paclobutrazol PubChem Compound Summary - Paclobutrazol http://www.pesticideinfo.org/ - PaclobutrazolKEGG (Kyoto Encyclopedia of Genes and Genomes) - Paclobutrazol http://www.ebi.ac.uk/ - Paclobutrazol http://www.ncbi.nlm.nih.gov/ - Paclobutrazol Local: Some commercial growth retardants are;
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SALES SPECIFICATION | ||
APPEARANCE |
white to light grey crystalline powder | |
ASSAY |
95.0% min |
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ACIDITY |
0.5% max |
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Loss on drying |
1.0% max |
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INSOLUBLES |
0.5% max (in acetone) |
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TRANSPORTATION | ||
PACKING |
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HAZARD CLASS | 4.1 (Packing Group: II) | |
UN NO. | 1325 | |
OTHER INFORMATION | ||
Hazard Symbols: XN, Risk Phrases: 22, Safety Phrase: 36 |
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GENERAL DESCRIPTION OF PLANT HORMONE |
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Auxin is one of
five (or more) major plant hormones (Auxin, Cytokinins, Gibberellins, Ethylene
and Abscisic acid) which affect numerous plant growth processes functions
including cell division and elongation, autumnal loss of leaves, and the
formation of buds, roots, flowers, and fruit. Auxin action is inhibited by
light which is an important role of the growth of stems toward light
(phototropism), against the force of gravity (geotropism) and positively
hydrotropic (moisture-seeking). The cells exposed to light don't grow as quickly
as those on the shaded side, and thus the plant grows toward the light source.
Auxins usually have a ring system with at least one double bond and attached by
a side-chain that terminates in a carboxyl group. Indole acetic acid is the
exact structure of Auxin activity. Parent compounds of auxin action are;
Cytokinin is a N6-substituted adenines acting as phytohormones such as kinetin, zeatin, 6-isopentenyladenine, benzyl adenine. The principal functions are stimulate cell division in concert with auxin (cytokinesis) and influence the pathway of tissue differentiation (organogenesis). 6-Benzylaminopurine is the first generation synthetic cytokinin which elicits plant growth and development responses setting blossoms and stimulating fruit richness by stimulating cell division. Active cytokinin ingredients include:
Other Plant Growth Regulators include:
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