Cobalt(II) thiocyanate
Chemical compound From Wikipedia, the free encyclopedia
Cobalt(II) thiocyanate is an inorganic compound with the formula Co(SCN)2.[1] The anhydrous compound is a coordination polymer with a layered structure. The trihydrate, Co(SCN)2(H2O)3, is a isothiocyanate complex used in the cobalt thiocyanate test (or Scott test) for detecting cocaine. The test has been responsible for widespread false positives and false convictions.[2][3]
Co2+ [N≡C−S−]2 | |
2.png) | |
| Identifiers | |
|---|---|
| |
3D model (JSmol) |
|
| ChemSpider | |
| ECHA InfoCard | 100.019.234 |
| EC Number |
|
PubChem CID |
|
| UNII | |
CompTox Dashboard (EPA) |
|
| |
| |
| Properties | |
| C2CoN2S2 | |
| Molar mass | 175.098 g/mol |
| Density | 2.484 g/cm3 |
| +11,090·10−6 cm3/mol | |
| Hazards | |
| GHS labelling: | |
  | |
| Warning | |
| H302, H312, H332, H410 | |
| P261, P264, P270, P271, P273, P280, P301+P312, P302+P352, P304+P312, P304+P340, P312, P322, P330, P363, P391, P501 | |
| Safety data sheet (SDS) | External MSDS |
| Related compounds | |
Other anions |
Cobalt(II) cyanate |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
| |
Structure and preparation
2_Xray.jpg)
The structures of Co(SCN)2 and its hydrate Co(SCN)2(H2O)3 have been determined using X-ray crystallography.[1] Co(SCN)2 forms infinite 2D sheets as in the mercury(II) thiocyanate structure type, where as Co(SCN)2(H2O)3 consists of isolated tetrahedral Co(SCN)2(H2O)2 centers and one equivalent of water of crystallization.[4]
The hydrate may be prepared by the salt metathesis reactions, such as the reaction of aqueous cobalt(II) sulfate and barium thiocyanate to produce a barium sulfate precipitate, leaving the hydrate of Co(SCN)2 in solution:[4]
- CoSO4 + Ba(SCN)2 → BaSO4 + Co(SCN)2
or the reaction of the hexakisacetonitrile cobalt(II) tetrafluoroborate and potassium thiocyanate, precipitating KBF4
- [Co(NCMe)6](BF4)2 + 2KSCN → 2KBF4 + Co(SCN)2.
The anhydrate can then be prepared via addition of diethylether as an antisolvent.[1]
Cobalt thiocyanate test
Detailed procedures for the cobalt thiocyanate test, often sold as the "morris reagent" are available. The reagent consists of 2% cobalt thiocyanate dissolved in dilute acid.[5] Glycerol is often added to stabilise the cobalt complex, ensuring it only goes blue when in contact with an analyte and not due to drying.[6]
Addition of the cobalt thiocyanate reagent to cocaine hydrochloride results in the surface of the particles turning a bright blue (faint blue for cocaine base). The solution changes back to pink upon adding some hydrochloric acid. Addition of chloroform, results in a blue organic layer for both cocaine hydrochloride and cocaine base. Diphenhydramine and lidocaine also give blue organic layers. These compounds are known false positives for cocaine. Lidocaine is commonly used to adulterate or mimic cocaine due to its local anaesthetic effect.
If the procedure is adjusted to basify the sample rather than acidifying it, the test can be used to test for ketamine hydrochloride.[7]
References
Wikiwand - on
Seamless Wikipedia browsing. On steroids.