Buy Chloroform trichloromethane Cas 67-66-3
Buy Chloroform trichloromethane Cas 67-66-3
Chloroform,[9] or trichloromethane (often abbreviated as TCM), is an organochloride with the formula CHCl3 and a common solvent. It is a volatile, colorless, sweet-smelling, dense liquid produced on a large scale as a precursor to refrigerants and polytetrafluoroethylene (PTFE).[10] Chloroform was once used as an inhalational anesthetic between the 19th century and the first half of the 20th century.[11][12] It is miscible with many solvents but it is only very slightly soluble in water (only 8 g/L at 20°C). Buy Chloroform trichloromethane Cas 67-66-3
Structure and name
The molecule adopts a tetrahedral molecular geometry with C3v symmetry.[13] The chloroform molecule can be viewed as a methane molecule with three hydrogen atoms replaced with three chlorine atoms, leaving a single hydrogen atom. Buy Chloroform trichloromethane Cas 67-66-3
The name “chloroform” is a portmanteau of terchloride (tertiary chloride, a trichloride) and formyle, an obsolete name for the methylylidene radical (CH) derived from formic acid.[14]
Natural occurrence
Many kinds of seaweed produce chloroform, and fungi are believed to produce chloroform in soil.[15] Abiotic processes are also believed to contribute to natural chloroform productions in soils, although the mechanism is still unclear.[16]
History
Chloroform was synthesized independently by several investigators c. 1831: Buy Chloroform trichloromethane Cas 67-66-3
- Moldenhawer, a German pharmacist from Frankfurt an der Oder, appears to have produced chloroform in 1830 by mixing chlorinated lime with ethanol; however, he mistook it for Chloräther (chloric ether, 1,2-dichloroethane).[17][18]
- Samuel Guthrie, a U.S. physician from Sackets Harbor, New York, also appears to have produced chloroform in 1831 by reacting chlorinated lime with ethanol, and noted its anaesthetic properties; however, he also believed that he had prepared chloric ether.[19][20][21]
- Justus von Liebig carried out the alkaline cleavage of chloral. Liebig incorrectly states that the empirical formula of chloroform was C2Cl5 and named it “Chlorkohlenstoff” (“carbon chloride”).[22][23]
- Eugène Soubeiran obtained the compound by the action of chlorine bleach on both ethanol and acetone.[24]
In 1834, French chemist Jean-Baptiste Dumas determined chloroform’s empirical formula and named it:[25] “Es scheint mir also erweisen, dass die von mir analysirte Substanz, … zur Formel hat: C2H2Cl6.” (Thus it seems to me to show that the substance I analyzed … has as [its empirical] formula: C2H2Cl6.). [Note: The coefficients of his empirical formula should be halved.] … “Diess hat mich veranlasst diese Substanz mit dem Namen ‘Chloroform’ zu belegen.” (This had caused me to impose the name “chloroform” upon this substance [i.e., formyl chloride or chloride of formic acid].) Buy Chloroform trichloromethane Cas 67-66-3
In 1835, Dumas prepared the substance by alkaline cleavage of trichloroacetic acid.
In 1842, Robert Mortimer Glover in London discovered the anaesthetic qualities of chloroform on laboratory animals.[26]
In 1847, Scottish obstetrician James Y. Simpson was the first to demonstrate the anaesthetic properties of chloroform (provided by local pharmacist William Flockhart of Duncan, Flockhart and company,[27]) in humans, and helped to popularize the drug for use in medicine.[28]
The application of chloroform remained dangerous, and many deaths occurred through accidental overdose.[29][30] In 1848, John Snow developed an inhaler that regulated the dosage.[29]
By the 1850s, chloroform was being produced on a commercial basis.[30] An apparatus that could apply it safely and controllably was invented by Joseph Thomas Clover in 1862.[31][32]
In Britain, about 750,000 doses a week were being produced by 1895,[30] using the Liebig procedure, which retained its importance until the 1960s. Today, chloroform – along with dichloromethane – is prepared exclusively and on a massive scale by the chlorination of methane and chloromethane
Chloroform CAS:67-66-3 EC:200-663-8
Chloroform is a common laboratory reagent favored for use as a solvent due to the compounds relative unreactivity and miscibility with most organic compounds. Chloroform is also used in organic synthesis as a source for CCl2. In the swine tracheal smooth muscle, chloroform has been demonstrated to directly and in a concentration dependent manner induce contractions. It has been observed that Chloroform can release Ca2+ from ryanodine sensitive receptors in chloroform-induced contraction in swine tracheal smooth muscle. At concentrations of 100 and 250 ppm in mouse splenocyte, basal proliferation was increased yet a decrease in circulating neutrophils was documented.
Chloroform, with the chemical formula CHCl3, is a trichloromethane derivative, a dense, colorless, volatile liquid known for its distinctive sweet smell. Historically significant as an anesthetic, chloroform′s use today is predominantly in industrial and research settings due to its potency and risks associated with exposure. In scientific research, chloroform serves primarily as a solvent due to its ability to dissolve many organic compounds that are otherwise insoluble in water, making it invaluable in the extraction and purification of biochemicals like alkaloids, fats, oils, and some resins. Its non-polar nature allows it to participate in phase separation techniques, particularly in liquid-liquid extraction processes. When mixed with water, chloroform undergoes phase separation, enabling the selective dissolution of compounds based on their solubility in the chloroform phase versus the aqueous phase. This characteristic is extensively utilized in the purification of large biomolecules and in the preparation of samples for analysis in fields such as environmental science, where it is used to extract pollutants from water samples before analysis. Additionally, in organic synthesis, chloroform acts as a source of the dichlorocarbene (:CCl2) group when treated with strong base. This reactive intermediate is employed in the synthesis of various organic compounds through reactions such as the formation of dichlorocyclopropanes from alkenes, illustrating its pivotal role in facilitating complex chemical transformations.
Chloroform (CAS 67-66-3) References
- Role of ryanodine receptors in chloroform-induced contraction in Swine tracheal smooth muscle. | Lin, YR., et al. 2002. Toxicol Appl Pharmacol. 183: 146-51. PMID: 12387754
- Immunotoxicological profile of chloroform in female B6C3F1 mice when administered in drinking water. | Auttachoat, W., et al. 2009. Drug Chem Toxicol. 32: 77-87. PMID: 19514942
- Chloroform exposure in air and water in Swedish indoor swimming pools-urine as a biomarker of occupational exposure. | Ragnebro, O., et al. 2023. Ann Work Expo Health. 67: 876-885. PMID: 37339253
- Toluene-driven anaerobic biodegradation of chloroform in a continuous-flow bioelectrochemical reactor. | Tucci, M., et al. 2023. Chemosphere. 338: 139467. PMID: 37437617
- Efficient and Reversible Separation of Chloroform from Chlorinated Hydrocarbons and Water Utilizing a Two-Dimensional Coordination Network. | Li, GB., et al. 2023. ACS Appl Mater Interfaces. 15: 37602-37608. PMID: 37504065
- Cytotoxicity and genotoxicity evaluation of chloroform using Vicia faba roots. | Li, X., et al. 2023. Toxicol Ind Health. 39: 603-612. PMID: 37518894
- Anthropogenic Chloroform Emissions from China Drive Changes in Global Emissions. | An, M., et al. 2023. Environ Sci Technol. 57: 13925-13936. PMID: 37656597
- Chloroform in food samples from 2014 Canadian total diet study: occurrence and dietary exposure. | Cao, XL., et al. 2024. Food Addit Contam Part A Chem Anal Control Expo Risk Assess. 41: 143-150. PMID: 38193981
- Chloroform associated with bone mineral density and bone mineral content in adults: A population-based cross-sectional research. | Li, L., et al. 2024. PLoS One. 19: e0290132. PMID: 38427675
GNMT, Hemoglobin, KRTAP4-13, Olfr310, Olfr318, Olfr32, P5CR2, PEPD, Prealbumin, and TALK-1.
ADHα, Adh1, ADH7, ASIC3, BIGM103, COX6b1, GlyR α3, Hemoglobin α1, Olfactorin, RyR-1, TASK-1, TASK-5, Tim17B, V1RC3, V1RC33, V1rc7, V1RD1, and V1RD11.
Chloroform, or trichloromethane (often abbreviated as TCM), is an organic compound with the formula CHCl3 and a common solvent. It is a very volatile, colorless, strong-smelling, dense liquid produced on a large scale as a precursor to refrigerants and in turn, PTFE. Chloroform is a trihalomethane that serves as a powerful anesthetic, euphoriant, anxiolytic, and sedative when inhaled or ingested. Chloroform was used as an anesthetic between the 19th century and the first half of the 20th century. It is miscible with many solvents but it is only very slightly soluble in water (only 8 g/L at 20 °C).
Chloroform trichloromethane CAS 67 66 3
SDS: Please Contact Genprice for SDS
COA: Please Contact Genprice for Certificate of Analysis
Humidity Content: As specified on the COA
Specific Gravity at 25°: As specified on COA
Appearance: As specified on the SDS
Safety Hazardous: Depending on the Concentration
Impurity: As specified on the SDS
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