Ads
related to: spectracide lawn weed killer directions- Landscape Weeds
Kill Weeds in Your Landscape
While Comfortably Guarding The Good
- Driveway & Patio Weeds
Kill & Prevent Weeds and Grasses in
Driveway, Patios & Other Hardscapes
- Product Picker
Let Us Help You Choose The Right
Products To Kill Your Weeds & Bugs!
- Refills
Refill & Reuse Your Current
Roundup® Sprayer and Bottles
- Control Lawn Weeds & Bugs
Shop Roundup® to Help Control
Your Lawn Weeds & Bugs
- Poison Ivy & Tough Brush
Kills Even The Toughest Weeds
To The Root, So It Won't Come Back
- Landscape Weeds
Search results
Results From The WOW.Com Content Network
The type of weed will clue you in on when to apply weed killer to the lawn. ... "Not following the labeled instructions can cause long-term serious illnesses or even death to humans and animals ...
Imazaquin inhibits the acetohydroxy acid synthase (AHAS) enzyme accountable for synthesis of the amino acids valine, leucine, and isoleucine. When applied, imazaquin halts weed growth which eventually kills the weed or causes the weed to die due to its incapability to compete with surrounding vegetation.
In January 2005, Rayovac purchased United Industries Corporation for about $476 million in cash and stock. Brands included in United Industries were Vigoro, Spectracide and Sta-Green lawn products, Cutter, Hot Shot and Repel insect control products, and pet supply products with the Marineland, Perfecto, and Eight in One brands. [9]
2,4-Dichlorophenoxyacetic acid is an organic compound with the chemical formula Cl 2 C 6 H 3 OCH 2 CO 2 H.It is usually referred to by its ISO common name 2,4-D. [4] It is a systemic herbicide that kills most broadleaf weeds by causing uncontrolled growth, but most grasses such as cereals, lawn turf, and grassland are relatively unaffected.
Dimethyl tetrachloroterephthalate (DCPA, with the main trade name Dacthal) is an organic compound with the formula C 6 Cl 4 (CO 2 CH 3) 2.It is the dimethyl ester of tetrachloroterephthalic acid, used as a preemergent herbicide with the ISO common name chlorthal-dimethyl.
According to the German Patent bureau, the industrial synthesis of diazinon is as follows: β-isobutyrylaminocrotonic acid amine was cyclized with NaOR (R is either a hydrogen or aliphatic chain of 1 to 8 carbons) in a mixture of 0 to 100% by weight of water and an alcohol having 1 to 8 carbon atoms, above 90°C (but below the boiling point of the mixture used).