methyl iodide

Methyl iodide is now registered in 47 other states.

In the five years methyl iodide has been on the market, it has seen relatively little use.

The use of methyl iodide as a fumigant has drawn concern.

And later its replacement methyl iodide was pulled off the market after numerous public protests.

A lawsuit was filed in 2011 challenging California's approval of methyl iodide.

Only one strawberry farmer in California used methyl iodide in 2011.

The sodium assists the reaction of the zinc with the methyl iodide.

Methyl iodide is an excellent substrate for S2 substitution reactions.

It is made by reacting a sodium amalgam with methyl iodide.

Also methyl iodide at a level indicative of marine-dominant photosynthesis.

Methyl iodide was approved as a pesticide in California that December.

In April, the state issued a notice to approve methyl iodide with an exposure limit of 96 parts per billion for workers.

Hence the oxidative addition of methyl iodide is proposed as rate-determining step.

For example, reaction of a square planar complex with methyl iodide:

Methyl iodide is injected into soil, kills bugs, weeds and plant diseases.

"Arysta saw the writing on the wall and chose to pull their cancer-causing methyl iodide product."

In March 2012, the manufacturer voluntarily pulled methyl iodide products from the market, citing issues of economic viability.

Managers at the agency say it's not up to scientists to decide whether methyl iodide is approved and at what levels.

For example, methyl iodide can be prepared from methanol, red phosphorus, and iodine.

Iodine, methyl iodide, and 1,2-Dibromoethane are common activating agents.

The reaction mechanism is first-order with respect to methyl iodide and the catalyst (1).

Since it was approved in 2007 by the Environmental Protection Agency, methyl iodide had seen little use across the nation.

The methionine derivative could be obtained by using only one mol of methyl iodide.

Dose response of weeds to methyl iodide and methyl bromide.

An alkylating agent (methyl iodide in the case of Fráter's publication) is then added.