α-Chloralose
Synonym(s):α-Chloralose;1,2-O-(2,2,2-Trichloroethylidene)-α-D -glucofuranose;Anhydro-D -glucochloral;Chloralose
- CAS NO.:15879-93-3
- Empirical Formula: C8H11Cl3O6
- Molecular Weight: 309.53
- MDL number: MFCD00005542
- EINECS: 240-016-7
- SAFETY DATA SHEET (SDS)
- Update Date: 2024-11-01 18:09:03
What is α-Chloralose?
Description
Chloralose, (R)-1,2-O-(2,2,2-trichloroethylidene)-
α-D-glucofuranose, is a crystalline powder which is soluble in water,
fairly soluble in alcohol, diethyl ether, glacial acetic acid,
sparingly soluble in chloroform, practically insoluble in
petroleum ether.
Chloralose is produced by reaction of glucose with waterfree
chloral under heating (21).
Chemical properties
needle-like crystals or powder
The Uses of α-Chloralose
Coating seeds to protect them from birds.
The Uses of α-Chloralose
Chloralose is used for the control of rodents, particularly mice, and as a bird repellent and a bird narcotic.
The Uses of α-Chloralose
It has been employed widely as an animal anesthetic in the laboratory setting. alpha-chloralose is a true anesthetic or an immobilizing agent with sedative-hypnotic properties has important implications. Canada geese (Branta canadensis) and blue geese (Chen caerulescens) were caught with alpha-chloralose, an oral hypnotic administered on bait. Wild turkeys (Meleagris gallopavo) were captured with alpha-chloralose, an oral anesthetic.
What are the applications of Application
α-Chloralose is a compound studied for its effect on presynaptic GABAA receptors
Hazard
May cause addiction, highly toxic.
Safety Profile
Poison by ingestion, subcutaneous, and intraperitoneal routes. Questionable carcinogen with experimental tumorigenic data. When heated to decomposition it emits toxic fumes of Cl-.
Metabolic pathway
Chloralose is effectively a chloral generator which, in turn, affords trichloroethanol by metabolism. This is the narcotic agent. Sleep is induced in mice before death and therefore the compound is regarded as a humane mouse killer. It is particularly effective when a quick clearout is required but there is evidence that mice can become tolerant.
Degradation
Chloralose is hydrolysed by acid and base to glucose and chloral (2, trichloroacetaldehyde).
Properties of α-Chloralose
Melting point: | 178-182 °C |
alpha | 18 º (c=2, 95% C2H5OH) |
Boiling point: | 424.33°C (rough estimate) |
Density | 1.6066 (rough estimate) |
vapor pressure | Negligible at room temperature |
refractive index | 1.5320 (estimate) |
solubility | ethanol: 10 mg/mL or yellow-brown, clear to slightly hazy, colorless to faintly yellow |
form | neat |
pka | 12.89±0.60(Predicted) |
form | Solid |
color | White to Almost white |
optical activity | [α]20/D +17±2°, 5 hr, c = 2% in ethanol |
Water Solubility | 0.44 g/100 mL (15 ºC) |
Merck | 14,2072 |
BRN | 85418 |
Stability: | Stable. Incompatible with strong oxidizing agents. |
CAS DataBase Reference | 15879-93-3(CAS DataBase Reference) |
EPA Substance Registry System | Chloralose (15879-93-3) |
Safety information for α-Chloralose
Signal word | Danger |
Pictogram(s) |
Skull and Crossbones Acute Toxicity GHS06 Environment GHS09 |
GHS Hazard Statements |
H301:Acute toxicity,oral H332:Acute toxicity,inhalation H336:Specific target organ toxicity,single exposure; Narcotic effects H410:Hazardous to the aquatic environment, long-term hazard |
Precautionary Statement Codes |
P261:Avoid breathing dust/fume/gas/mist/vapours/spray. P264:Wash hands thoroughly after handling. P264:Wash skin thouroughly after handling. P270:Do not eat, drink or smoke when using this product. P273:Avoid release to the environment. P301+P310:IF SWALLOWED: Immediately call a POISON CENTER or doctor/physician. |
Computed Descriptors for α-Chloralose
Abamectin manufacturer
JSK Chemicals
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