Nomenclature

Type Plant Growth Regulator
Common name Paclobutrazol
Other name
Iupac name

(2RS,3RS)-1-(4-chlorophenyl)-4,4-dimethyl-2-(1H-1,2,4-triazol-1-yl)pentan-3-ol

Formulation type
Formulation TypeOptions
97%TC  
25%SC  
Chemical Abstracts Name

(R*,R*)-(?-b-[(4-chlorophenyl)methyl]-a-(1,1-dimethylethyl)-1H-1,2,4-triazole-1-ethanol

CAS RN 76738-62-0
EEC no
Official code
Development code

Physical Chemistry

M.F.

C15H20ClN3O

Structure M
Mol. wt 293.8
Appearance

White, crystalline solid.

M.p.

165-166 ℃

B.p.
V.p.

0.001 mPa (20 ℃)

F.p.
S.g./density

1.22 g/ml

Solubility

In water 26 mg/l (20 ℃). In acetone 110, cyclohexanone 180, dichloromethane 100, hexane 10, xylene 60, methanol 150, propylene glycol 50 (all in g/l, 20 ℃).

Stability

Stable for more than 2 years at 20 ℃, and more than 6 months at 50 ℃. Stable to hydrolysis (pH 4-9), and not degraded by u.v. light (pH 7, 10 days).

Henry

1.13 ×10-5 Pa m3 mol-1 (calc.)

KowlogP

= 3.2

Pka

Applications

Biochemistry

Inhibits gibberellin and sterol biosynthesis, and hence the rate of cell division.

Mode of Action

Plant growth regulator taken up into the xylem through the leaves, stems, or roots, and translocated to growing sub-apical meristems. Produces more compact plants and enhances flowering and fruiting.

Uses

Used on fruit trees to inhibit vegetative growth and to improve fruit set; on pot-grown ornamentals and flower crops (e.g. chrysanthemums, begonias, freesias, poinsettias and bulbs) to inhibit growth; on rice to increase tillering, reduce lodging, and increase yield; on turf to retard growth; and on grass seed crops to reduce height and prevent lodging. To be applied as a foliar spray, as a soil drench, or by trunk injection. Has some fungicidal activity against mildew and rusts.

Phytotoxicity

Non-phytotoxic, though it intensifies greening. Some spotting has been noted on periwinkle foliage at higher temperatures.

Compatibility
General details

Mammalian Toxicology

Reviews

Product analysis by glc or by hplc. Residues determined by tlc.

Oral

Acute oral LD50 for male rats 2000, female rats 1300, male mice 490, female mice 1200, guinea pigs 400-600, male rabbits 840, female rabbits 940 mg/kg.

Skin & Eye

Acute percutaneous LD50 for rats and rabbits >1000 mg/kg. Mild skin irritant; moderate eye irritant (rabbits). Not a skin sensitiser (guinea pigs).

Inhalation

LC50 (4 h) for male rats 4.79, female rats 3.13 mg/l air.

Noel

(1 y) for dogs 75 mg/kg daily; (2 y) for rats 250 mg/kg diet.

ADI

(JMPR) 0.1 mg/kg b.w. [1988].

Toxicity class

WHO (a.i.) III; EPA (formulation) IV

EC hazard

Ecotoxicology

Birds

Acute oral LD50 for mallard ducks >7900 mg/kg.

Fish

LC50 (96 h) for rainbow trout 27.8 mg/l. NOEC 3.3 mg/l.

Daphnia

LC50 (48 h) 33.2 mg/l.

Algae

EC50 (cell volume) for Chlorella fusca 180 umol/l (Pestic. Sci.,47, 337 (1996)).

Worms

Environmental Fate

Plants
Animals
Soil/environment

Soil DT50 0.5-1.0 y in general; in calcareous clay loam (pH 8.8, 14% o.m.), DT50 <42 d; in coarse sandy loam (pH 6.8, 4% o.m.), DT50 >140 d.

Miscellaneous

Analysis

Product analysis by glc or by hplc. Residues determined by tlc.

Packing