First, because thiocyanate is also toxic, although to a lesser degree.

Note: this compound may also be recognized as guanidine thiocyanate.

Reliance on cassava as a carbohydrate provides a source of thiocyanate in some areas.

Mercury thiocyanate has a few uses in chemical synthesis.

Iron is determined colorimetrically, usually with thiocyanate, which gives a red colour in acid solution.

Perchlorate and thiocyanate are drugs that can compete with iodine at this point.

The low solubility product of mercury thiocyanate causes it to precipitate from solution.

Rhodanese can convert cyanide into the relatively harmless compound thiocyanate.

The first chemical for hypertension, sodium thiocyanate, was used in 1900 but had many side effects and was unpopular.

Inhibition of this step requires competitive inhibitors, such as perchlorate and thiocyanate.

The thiocyanate is the leaving group.

By age 14, he says, "I was studying the isomerization of benzyl thiocyanate to the isocyanate."

The thiocyanate is treated with sulfuric acid and then hydrolyzed with ice water.

Ammonium thiocyanate can also be used to determine the iron content in soft drinks by colorimetry.

The main method involves the thermal rearrangement of methyl thiocyanate:

Reaction with other pseudohalides such as azide, cyanide, and thiocyanate are possible as well.

The product is further processed (without being isolated) by a solution of potassium thiocyanate in hydrochloric acid.

Melam was discovered by Liebig in 1834 from the residue of heating ammonium thiocyanate.

Ferric thiocyanate has been suggested, and sulfur was said to have been detected in the mineral.

This reaction is important for the decontamination of cyanide, since the thiocyanate formed is relatively harmless.

Calcium hexamine thiocyanate is a nasal preparation.

Sodium thiocyanate is employed to convert alkyl halides into the corresponding alkylthiocyanates.

Ammonium thiocyanate is stable in air; however, upon heating it isomerizes to thiourea:

Sodium thiocyanate crystallizes in an orthorhombic cell.

This sample provided scientists a first-hand opportunity to study the virus, which was inactivated with guanidinium thiocyanate before transport.

It is usual, therefore, to add a salt such as sodium thiocyanate.

Last of the three was the best of them all, cobalt thiocyanate.

A significant inductive effect was produced by thiosulphate and thiocyanate.

Note: this compound may also be recognized as guanidine thiocyanate.

He also had a slight increase in urinary thiocyanate.

"It may even use the thiocyanate to exist."

Apart from the reaction you've carried out, thiocyanate can be used in the synthesis of more complex compounds.

Thiocyanate shares its negative charge approximately equally between sulfur and nitrogen.

Perchlorate and thiocyanate are drugs that can compete with iodine at this point.

Copper(I) thiocyanate is white solid which is stable in air under standard conditions.

As such, foodstuffs containing thiocyanate are best avoided by hypothyroid patients.

Iron is determined colorimetrically, usually with thiocyanate, which gives a red colour in acid solution.

Similarly, Co gives a blue complex with thiocyanate.

Many of these effects are believed to be controlled by the antithyroid activity of thiocyanate.

Ethyl thiocyanate is a chemical compound used as an agricultural insecticide.

Calcium hexamine thiocyanate is a pharmaceutical drug that has been used in nasal preparations.

Thiocyanate is known to be an important part in the biosynthesis of hypothiocyanite by a lactoperoxidase.

Finally, thiocyanate is produced which is a very unstable radical that can lead to cellular damage.

This solution forms a copper thiocyanate precipitate which is white and can be used in a titration.

Statistically significant decreases in serum thiocyanate levels followed participation in each of the three programs.

The thiocyanate is the leaving group.

The first chemical for hypertension, sodium thiocyanate, was used in 1900 but had many side effects and was unpopular.

Inhibition of this step requires competitive inhibitors, such as perchlorate and thiocyanate.

The cyclopentadienyl directing the thiocyanate to bond through its softer Sulphur donor.

Copper(I) thiocyanate is precipitated as a white powder.

Thiocyanate used to be known as rhodanide (from a Greek word for rose) because of the red colour of its complexes with iron.

In 1937, he patented a technique for synthesizing novel rhodanide- and cyanate-based compounds which showed bactericide and insecticide activity.

Thiocyanate (also known as rhodanide) is the anion [SCN].

It was first discovered in 1877 by Marceli Nencki who named it "Rhodaninsaure" in reference to its synthesis from ammonium rhodanide (in modern chemistry ammonium thiocyanate) and chloroacetic acid in water.