Thursday, March 29, 2012

What is Dichlorotris(triphenylphosphine)ruthenium(II)?

Dichlorotris(triphenylphosphine)ruthenium(II) is a allocation circuitous of ruthenium. This amber amber solid is a forerunner to added complexes including those acclimated as constant catalysis.
RuCl2(PPh3)3 facilitates oxidations, reductions, cross-couplings, cyclizations, and isomerization. It is acclimated in the Kharasch accession of chlorocarbons to alkenes.
Dichlorotris(triphenylphosphine)ruthenium(II) serves as a precatalyst for the hydrogenation of alkenes, nitro compounds, ketones, carboxylic acids, and imines. On the added hand, it catalyzes the blaze of alkanes to tertiary alcohols, amides to t-butyldioxyamides, and tertiary amines to α-(t-butyldioxyamides) application tert-butyl hydroperoxide. Application added peroxides, oxygen, and acetone, the agitator can burn alcohols to aldehydes or ketones. Application dichlorotris(triphenylphosphine)ruthenium(II) the N-alkylation of amines with alcohols is aswell accessible
A ruthenium-phosphine complex represented by formula (I): ##STR1## wherein R represents a hydrogen atom, a methyl group, or a methoxy group; S represents a tertiary amine; when y is 0, then x is 2, z is 4, and p is 1; and when y is 1, then x is 1, z is 1, and p is 0. The complex is inexpensive and exhibits excellent performance as a catalyst for various organic syntheses, and particularly asymmetric hydrogenation.
Phosphine (IUPAC name: phosphane) is the admixture with the actinic blueprint PH3. It is a colorless, flammable, baneful gas. Pure phosphine is odorless, but abstruse brand samples accept a awful abhorrent odor like garlic or adulteration fish, due to the attendance of commissioned phosphine and diphosphine (P2H4). With traces of P2H4 present, PH3 is spontaneously combustible in air, afire with a beaming flame. Phosphines are aswell a accumulation of organophosphorus compounds with the blueprint R3P (R = amoebic derivative). Organophosphines are important in catalysts area they circuitous to assorted metal ions; complexes acquired from a chiral phosphine can activate reactions to accord chiral products.
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Wednesday, March 28, 2012

What is 5-Bromo-2-fluorobenzaldehyde?

Benzaldehyde (C6H5CHO) is an amoebic admixture consisting of a benzene ring with a formyl substituent. It is the simplest ambrosial aldehyde and one of the a lot of industrially useful. This achromatic aqueous has a appropriate affable almond-like odor. In fact, benzaldehyde is the primary basic of absinthian almond oil and can be extracted from a amount of added accustomed sources. Benzaldehyde was aboriginal extracted from absinthian almonds in 1803 by the French pharmacist Martrès. In 1832 German chemists Friedrich Wöhler and Justus von Liebig aboriginal actinic benzaldehyde.
Benzaldehyde can be acquired by abounding processes. In the 1980s, an estimated 18 actor kilograms were produced annually in Japan, Europe, and North America, a akin that can be affected to continue. Currently aqueous appearance chlorination and blaze of toluene are the capital routes. Numerous added methods accept been developed, such as the fractional blaze of benzyl alcohol, acrid hydrolysis of benzal chloride, and the carbonylation of benzene.
Benzaldehyde can be actinic from cinnamaldehyde acquired from the oil of biscuit by refluxing in aqueous/alcoholic band-aid amid 90 °C and 150 °C with a abject (most frequently sodium carbonate or bicarbonate) for 5 to 80 hours, followed by beverage of the formed benzaldehyde. This acknowledgment aswell yields acetaldehyde.
Uses
Benzaldehyde is frequently active to advise almond flavor. Benzaldehyde is acclimated chiefly as a forerunner to added amoebic compounds, alignment from pharmaceuticals to artificial additives. The aniline dye malachite blooming is able from benzaldehyde and dimethylaniline. It is a forerunner to assertive acridine dyes as well. Via aldol condensations, benzaldehyde is adapted into derivatives of cinnamaldehyde and styrene.
First hydrocyanic acerbic is added to benzaldehyde, and the consistent nitrile is after hydrolysed to mandelic acid. (The arrangement aloft depicts alone one of the two formed enantiomers).
Glaciologists LaChapelle and Stillman appear in 1966 that benzaldehyde and N-heptaldehyde arrest the recrystallization of snow and accordingly the accumulation of abyss hoar. This analysis may anticipate avalanches acquired by ambiguous abyss chill layers. However, the chemicals are not in boundless use because they accident frondescence and alloy baptize supplies.
Benzaldehyde is a bee repellant and is acclimated to drive bees out of their hives if agriculture honey.
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Tuesday, March 27, 2012

What is Cholesteryl Acetate (Cholesterol acetate)?

Cholesteryl Acetate (Cholesterol acetate)
Molecularformula:C29H48O2
Cas No.:604-35-3
Molecularweight:428.7
Appearance: White powder
Melting  point: 112-115 ℃ Loss on
Drying: Less than 1%
Assay:  ≥97.0 %
Cholesteryl acetate was a flowing liquid exhibiting optical properties previously attributed only to crystals. The discovery brought into question the belief of the time that only three states of matter could exist (liquid, solid, and gas). More recently, liquid crystals such as cholesteryl acetate have come to be used in cosmetics, wrist watches, thermometers, propane tank volume indicators, video displays, and in the "mood rings" of the late 1970s fad.
Synthesis of cholesteryl acetate from cholesterol involves heating the cholesterol in a solution of acetic acid and acetic anhydride. Although synthesized in the laboratory and on a commercial scale, cholesteryl acetate exists as a naturally occurring substance as well. For example, it is found as one of the three cholesterol esters composing the outer cuticle layer lipid coating of the brown dog tick
Cholesteryl acetate disrupts the packing order of the DMPC acyl chains from 0 to ca. 35 mol% cholesterylacetate. As the concentration of cholesterylacetate is increased from ca. 14 to ca. 35 mol% the DMPC acyl chains become more ordered and cholesterylacetate appears to form a crystalline phase that remains inn suspension with the lecithin. As more cholesterylacetate is added, these crystalline regions become larger and begin to form a precipitate which is structurally identical to those particles which remain in suspension.
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Monday, March 26, 2012

What is Sodium tetrachloroaurate (III) dihydrate

Sodium tetrachloroaurate (III) dihydrate
CAS Number: 13874-02-7
Molecular Weight: 397.80
Molecular Formula: NaAuCl4•2H2O
Physical Appearance: Yellow to gold powder or crystals
Description
Sodium tetrachloroaurate (III) dihydrate is a water/alcohol soluble Au(I) complex that is formed from NaAuCl4. It has potential for application in chemotherapeutics.
Sodium Tetrachloroaurate(III) Dihydrate is generally immediately available in most volumes. High purity, submicron and nanopowder forms may be considered.
Sodium is a metallic element with a symbol Na, and atomic number 11. It is a soft, silvery-white, highly reactive metal and is a member of the alkali metals within "group 1". It has one stable isotope, 23Na.
Elemental sodium was first isolated by Humphry Davy in 1807 by passing an electric current through molten sodium hydroxide. Elemental sodium does not occur naturally on Earth, because it quickly oxidizes in air and is violently reactive with water, so it must be stored in a non-oxidizing medium, such as a liquid hydrocarbon. The free metal is used for some chemical synthesis, analysis, and heat transfer applications.
Characteristics
At room temperature, sodium metal is soft enough that it can be cut with a knife. In air, the bright silvery luster of freshly exposed sodium will rapidly tarnish. The density of alkali metals generally increases with increasing atomic number, but sodium is denser than potassium. Sodium is a fairly good conductor of heat.
Sodium changes color at high pressures, turning black at 1.5 megabar, becoming a red transparent substance at 1.9 megabar, and is predicted to become clearly transparent at 3 megabar. The high pressure allotropes are insulators and take the form of sodium electride.
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What is Kinetin?

Kinetin is a kind of cytokinin, a class of plant hormone that promotes cell division. Kinetin was originally isolated by Miller and Skoog et al. as a compound from autoclaved herring sperm DNA that had cell division-promoting activity. It was given the name kinetin because of its ability to induce cell division, provided that auxin was present in the medium. The story of the discovery of kinetin is a fascinating example of the twists and turns of scientific discovery. Kinetin is often used in plant tissue culture for inducing formation of callus (in conjunction with auxin) and to regenerate shoot tissues from callus (with lower auxin concentration).
For a long time, it was believed that kinetin was an artifact produced from the deoxyadenosine residues in DNA, which degrade on standing for long periods or when heated during the isolation procedure. Therefore, it was thought that kinetin does not occur naturally, but, since 1996, it has been shown by several researchers that kinetin exists naturally in the DNA of cells of almost all organisms tested so far, including human and various plants. The mechanism of production of kinetin in DNA is thought to be via the production of furfural — an oxidative damage product of deoxyribose sugar in DNA — and its quenching by the adenine base's converting it into N6-furfuryladenine, kinetin.
Since 1994, Kinetin has been thoroughly tested for its powerful anti-aging effects in human skin cells and other systems. At present, kinetin is one of the widely used components in numerous skin care cosmetics and cosmeceuticals, such as Valeant products kinerase . There are some reports published on other biological effects of kinetin in human beings, for example its effects as anti-platelet aggregation factor reducing thrombosis formation. In addition, it has been shown to be capable of correcting RNA mis-splicing in the disease of familial dysautonomia, in which exon 20 of IKBKAP is skipped instead of included in the disease, leading to insufficient levels of IKBKAP protein product as a result of frame-shift-induced nonsense-mediated decay.
Kinetin stimulates skin cells at the deepest layers of skin's surface to keep them healthier longer. It is Kinerase's signature ingredient that has successfully transformed women's skin for more than 10 years, visibly improving wrinkles, tone and texture.
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Specifications of Ammonium hexachloroiridate(III)

Ammonium hexachloroiridate(III)
CAS 15752-05-3
F.Weight. 459.06
Molecular Formula: Cl6H12IrN3
Synonyms: Ammonium chloroiridite, Triammonium hexachloroiridate, EINECS 239-842-0, CID161145, Iridate(3-), hexachloro-, triammonium
assay 99.99% trace metals basis
form solid
solubility H2O: slightly soluble
Ammonium Chloride, an inorganic compound with the formula NH4Cl, is a white crystalline salt, highly soluble in water. Solutions of ammonium chloride are mildly acidic. Sal ammoniac is a name of the natural, mineralogical form of ammonium chloride. The mineral is especially common on burning coal dumps (formed by condensation of coal-derived gases), but also on some volcanoes and liquorice. It is the product from the reaction of hydrochloric acid and ammonia.
Ammonium chloride is used as a flux in preparing metals to be tin coated, galvanized or soldered. It works as a flux by cleaning the surface of workpieces by reacting with the metal oxides at the surface to form a volatile metal chloride. For this purpose, it is sold in blocks at hardware stores for use in cleaning the tip of a soldering iron and can also be included in solder as flux.
Ammonium chloride is used as an expectorant in cough medicine. Its expectorant action is caused by irritative action on the bronchial mucosa. This causes the production of excess respiratory tract fluid which presumably is easier to cough up. Ammonium salts are an irritant to the gastric mucosa and may induce nausea and vomiting.
Ammonium chloride is used as a systemic acidifying agent in treatment of severe metabolic alkalosis, in oral acid loading test to diagnose distal renal tubular acidosis, to maintain the urine at an acid pH in the treatment of some urinary-tract disorders.
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Thursday, March 22, 2012

Where to get Oxycarbonyruodium chloride?

Ruthenium(III) chloride is the chemical compound with the formula RuCl3. "Ruthenium(III) chloride" more commonly refers to the hydrate RuCl3·xH2O. Both the anhydrous and hydrated species are dark brown or black solids. The hydrate, with a varying proportion of water of crystallization, often approximating to a trihydrate, is a commonly used starting material in ruthenium chemistry.
Properties
The anhydrous forms of Ruthenium(III) chloride are well characterized but rarely used. Crystalline material is usually prepared by heating powdered ruthenium metal to 700 °C under a 4:1 mixture of chlorine and carbon monoxide: the product is carried by the gas stream and crystallises upon cooling. RuCl3 exists is two crystalline modifications. The black α-form adopts the CrCl3-type structure with long Ru-Ru contacts of 346 pm. The dark brown metastable β-form crystallizes in a hexagonal cell; this form consists of infinite chains of face-sharing octahedra with Ru-Ru contacts of 283 pm. The β-form is irreversibly converted to the α-form at 450–600 °C.
RuCl3 vapour decomposes into the elements at high temperatures ; the enthalpy change at 750 °C (1020 K), ΔdissH1020 has been estimated as +240 kJ/mol.
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Specifications of 2-Amino-6-bromopyridine

2-Amino-6-bromopyridine
CAS Number: 19798-81-3
Molecular Weight: 173.01
Molecular Formula: C5H5BrN2
Synonyms 6-Bromo-2-pyridinamine
Physical Appearance: White to tan powder
Melting point 88-91 ºC
Description of 2-Amino-6-bromopyridine
Employed in an efficient one-pot synthesis of 7-azaindoles. Used in the synthesis of anti-HIV agents.
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Wednesday, March 21, 2012

What is Tetrakis(triphenylphosphine)palladium(0)?

Tetrakis(triphenylphosphine)palladium(0)
Synonyms Palladium(0)tetrakis(triphenylphosphine)
Molecular Formula C72H60P4Pd
Molecular Weight 1155.58
CAS Registry Number 14221-01-3
Melting point 103-107 ºC
Water solubility insoluble
Tetrakis(triphenylphosphine)palladium(0) is the chemical compound Pd[P(C6H5)3]4, often abbreviated Pd(PPh3)4, or even PdP4. It is a bright yellow crystalline solid that becomes brown upon decomposition in air.
Palladium is a chemical element with the chemical symbol Pd and an atomic number of 46. It is a rare and lustrous silvery-white metal discovered in 1803 by William Hyde Wollaston. He named it after the asteroid Pallas, which was itself named after the epithet of the Greek goddess Athena, acquired by her when she slew Pallas. Palladium, platinum, rhodium, ruthenium, iridium and osmium form a group of elements referred to as the platinum group metals (PGMs). These have similar chemical properties, but palladium has the lowest melting point and is the least dense of them.
Application
Catalyst for Negishi coupling, Suzuki coupling, Stille coupling, and Sonogashira coupling reaction
Catalyst for Buchwald-Hartwig amination reaction
Catalyst for the carbonylation of vinyl iodides
Catalyst for reduction reaction of aryl bromides
Catalyst for carbon-tin bond formation
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Tuesday, March 20, 2012

Uses of Cholesteryl pelargonate (Cholesterol pelargonate)?

Cholesteryl nonanoate, also called cholesteryl pelargonate, 3β-cholest-5-en-3-ol nonaoate or cholest-5-ene-3-β-yl nonanoate, is an ester of cholesterol and nonanoic acid. It is a liquid crystal material forming cholesteric liquid crystals with helical structure. It forms spherulite crystals.
Uses
It is used in some hair colors, make-ups, and some other cosmetic preparations. It is also used in some pleochroic dyes and together with e.g. cholesteryl oleyl carbonate and cholesteryl benzoate in some thermochromic applications.
Cholesteryl pelargonate (Cholesterol pelargonate) can be also used as a component of the liquid crystals used for liquid crystal displays.
Cholesterol is a steroid alcohol that is essentially insoluble in aqueous solutions. Cholesterol can be esterified with a fatty acid to form cholesteryl esters. The latter form discrete lipid droplets in cells, especially in cells of steroidogenic tissues, and in the lipid core of low-density lipoproteins in the blood. Cholesterol is a fatty lipid sparingly insoluble in water but soluble in a number of organic solvents. It is the most common sterol of eukaryotes which a key constituent of cell membranes and works as the precursor of bile acids, cholecalciferol (vitamin D)  and steroid hormones including cortisol, cortisone,  aldosterone and sex hormone progesterone in vertebrates. Cholesterol is used as an emulsifying agent in pharmaceuticals. The most cholesterols are synthesized by the liver and other tissues include the adrenal glands and reproductive organs. Some cholesterol  is absorbed from dietary sources. The largest concentration of cholesterol is in the myelin sheath that surrounds nerves and in the plasma membrane that surrounds all cells in vertebrates (25% of brain lipid is cholesterol).
Cholesterol can be esterified with a fatty acid to form cholesteryl esters which form discrete lipid droplets in cells, especially in cells of steroidogenic tissues, and in the lipid core of low-density lipoproteins in the blood. The collection on the walls of arteries interferes with the flow of blood. The High level of cholesterol in the blood is a major risk factor for coronary heart diseases. Cholesteric materials are liquid crystals of mesomorphic phase in which molecules are parallel to each other within the plane of a layer, but the direction is oriented in loose parallel lines to form a helix through the layers. Cholesteric materials are temperature sensitive and have color changing ability upon temperature
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Monday, March 19, 2012

What is N-Benzyl-4-(benzylamino)picolinamide?

N-Benzyl-4-(benzylamino)picolinamide
Synonyma: N-BENZYL-4-(BENZYLAMINO)PICOLINAMIDE;4-(Benzylamino)-N-benzylpyridine-2-carboxamide;4-(Benzylamino)-N-benzylpyridine-2-carboxamide 98%
Molecular Formula:C20H19N3O
CAS No.: 913836-29-0
Molecular weight:317.38436
Picolinamide, 2-pyridinecarboxylic acid amide, was found to be a strong inhibitor of poly (ADP-ribose) synthetase of nuclei from rat pancreatic islet cells. Another experiment using isolated pancreatic islets of rats showed that picolinamide protects against streptozotocin-induced depression of proinsulin synthesis as well as against streptozotocin-induced reduction of NAD content. The protection by picolinamide against the NAD depression was considered to be due to the blockage of an increased degradation of NAD mediated by a streptozotocin-induced increase in poly (ADP-ribose) synthetase activity.
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What is 4-Fluoro-2-methoxy-N-methylaniline?


4-Fluoro-2-methoxy-N-methylaniline
Molecular Formula:C8H10FNO
CAS No.:941294-13-9
N-methylaniline
is an aniline derivative. It is a toxic organic compound with the chemical formula C6H5NH(CH3). The substance exists as a colorless or slightly yellow viscous liquid, which is insoluble in water and brown when exposed to air. It is used as a latent and coupling solvent and is also used is as an intermediate for dyes, agrochemicals and other organic products manufacturing.
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Sunday, March 18, 2012

Properties and uses of Ruthenium(IV) oxide

Ruthenium(IV) oxide (RuO2) is a atramentous actinic admixture absolute the attenuate metal ruthenium and oxygen. The a lot of about acclimated O2 agitator is ruthenium(IV) oxide; however, affliction have to be taken back hydrates of this oxide exist.
RuO2 is about acclimated as a agitator in assorted automated applications or an electrode in electrochemical processes. RuO2 is awful acknowledging with abbreviation agents, due to its acerbic properties.
Properties
Ruthenium(IV) oxide takes on the rutile crystal structure, similar to titanium dioxide and several other metal oxides. Due to its structure, ruthenium(IV) oxide easily forms hydrates.
Ruthenium(IV) oxide is a (nearly black) purple crystalline solid at room temperature. The hydrates of RuO2 have a blue color to them.
Ruthenium oxide has great capacity to store charge when used in aqueous solutions. Average capacities of ruthenium(IV) oxide have reached 650 F/g when in H2SO4 solution and annealed at temperatures lower than 200 °C. In attempts to optimise its capacitive properties, prior work has looked at the hydration of ruthenium oxide, its crystallinity and particle size.
Uses
Ruthenium(IV) oxide is extensively used for the coating of titanium anodes for the electrolytic production of chlorine and for the preparation of resistors or integrated circuits.
Ruthenium(IV) oxide is a versatile catalyst and doping agent. Hydrogen sulfide can be split by light by using a photocatalyst of CdS particles doped with ruthenium(IV) oxide loaded with ruthenium dioxide. This may be useful in the removal of H2S from oil refineries and from other industrial processes. The hydrogen produced could be used to synthesize ammonia, methanol, and possibly fuel a future hydrogen economy.
Ruthenium (IV) oxide is being used as the main component in the catalyst of the Deacon process which produces chlorine by the oxidation of hydrogen chloride.It can be also used as active material in supercapacitor because has very high charge transfer capability.
Ruthenium oxide resistors can be used as sensitive thermometers in the temperature range .02<T<4K.
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Thursday, March 15, 2012

What is Silver Potassium Cyanide?

Description of Silver Potassium Cyanide
Silver Potassium Cyanide is poisonous and Used in silver plating, as a bactericide and in the manufacture of antiseptics. Not registered as a pesticide in the U.S.
Silver Potassium Cyanide is colorless crystalline compound, Silver Potassium Cyanide is highly soluble in water and has similar appearance to sugar. It is known among the few substances that form soluble compounds with gold. So, it is used in jewelry for chemical gilding & buffing. This substance can also be used in gold mining for the extraction of metal from ores, where sodium cyanide is more predominantly used.
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Specifications of 2,3-Difluoro-4-nitroanisole

2,3-Difluoro-4-nitroanisole
Molecular Formula:C7H5F2NO3
CAS No.:66684-59-1
Molecular Formula: C7H5F2NO3
Molecular Weight:189.12   
Melting point (oC): 96-99
o-Nitroanisole is reasonably anticipated to be a human carcinogen based on evidence of malignant tumor formation at multiple tissue sites in multiple species of experimental animals (For detasils See NTP, 1993).
When administered in the diet to male and female rats, o-nitroanisole induced increased incidences of mononuclear cell leukemia and neoplasms of the urinary bladder, kidney, and large intestine. When administered in the diet to male and female mice, o-nitroanisole induced increased incidences of benign and malignant hepatocellular neoplasms in males and increased incidences of hepatocellular adenomas in females.
PROPERTIES
O-nitroanisole is a colorless to slightly yellow liquid with a boiling point of 277°C and a melting point of 9-10°C. It is insoluble in water but is soluble in most organic solvents, including alcohol and ether. As a bulk chemical, o-nitroanisole is stable for two weeks at temperatures up to 60°C when stored protected from light. When heated to decomposition, o-nitroanisole emits toxic fumes of NOx.
USE
o-Nitroanisole is used primarily as a precursor to o-anisidine which is prepared by direct nitro-reduction. o-Anisidine is used extensively in the synthesis of azo dyes either directly after being converted to a diazonium salt or as a precursor for the preparation of dianisidine which is diazotized and coupled. Directly or indirectly, o-anisidine is used in the manufacture of over 100 azo dyes (For detasils See NTP, 1993). o-Nitroanisole has also been used as an intermediate for pharmaceuticals (IARC V.65, 1996).
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Wednesday, March 14, 2012

Differences between Palladium and Palladium acetylacetonate


Palladium acetylacetonate is a compound with formula Pd(C5H7O2)2. It is the palladium complex of acetylacetone. This compound is commercially available and used as a catalyst in organic synthesis.
Palladium Acetylacetonate is a Palladium source that is soluble in organic solvents. The high purity acetylacetonate anion complexes by bonding each oxygen atom to the metallic cation Acetylacetonate Packaging, Lab Quantityto form a chelate ring.Because of this property, Palladium Acetylacetonate is commonly used in various catalysts and catalytic reagents for organic synthesis. It is generally immediately available in most volumes.
Palladium is a chemical element with the chemical symbol Pd and an atomic number of 46. It is a rare and lustrous silvery-white metal discovered in 1803 by William Hyde Wollaston. He named it after the asteroid Pallas, which was itself named after the epithet of the Greek goddess Athena, acquired by her when she slew Pallas. Palladium, platinum, rhodium, ruthenium, iridium and osmium form a group of elements referred to as the platinum group metals (PGMs). These have similar chemical properties, but palladium has the lowest melting point and is the least dense of them.
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Tuesday, March 13, 2012

Functions of Cholesterol


Cholesterol, from the Greek chole- (bile) and stereos (solid) followed by the chemical suffix -ol for an alcohol, is an organic chemical substance classified as a waxy steroid of fat. It is an essential structural component of mammalian cell membranes and is required to establish proper membrane permeability and fluidity. In addition, cholesterol is an important component for the manufacture of bile acids, steroid hormones, and vitamin D. Cholesterol is the principal sterol synthesized by animals, in vertebrates it is formed predominantly in the liver. Small quantities are synthesized in other eukaryotes such as plants and fungi. It is almost completely absent among prokaryotes, i.e. bacteria.
Function
Cholesterol is required to build and maintain membranes; it modulates membrane fluidity over the range of physiological temperatures. The hydroxyl group on cholesterol interacts with the polar head groups of the membrane phospholipids and sphingolipids, while the bulky steroid and the hydrocarbon chain are embedded in the membrane, alongside the nonpolar fatty acid chain of the other lipids. Through the interaction with the phospholipid fatty acid chains, cholesterol increases membrane packing, which reduces membrane fluidity. In this structural role, cholesterol reduces the permeability of the plasma membrane to neutral solutes, protons, (positive hydrogen ions) and sodium ions.
Within the cell membrane, cholesterol also functions in intracellular transport, cell signaling and nerve conduction. Cholesterol is essential for the structure and function of invaginated caveolae and clathrin-coated pits, including caveola-dependent and clathrin-dependent endocytosis. The role of cholesterol in such endocytosis can be investigated by using methyl beta cyclodextrin (MβCD) to remove cholesterol from the plasma membrane. Recently, cholesterol has also been implicated in cell signaling processes, assisting in the formation of lipid rafts in the plasma membrane. Lipid raft formation brings receptor proteins in close proximity with high concentrations of second messenger molecules. In many neurons, a myelin sheath, rich in cholesterol, since it is derived from compacted layers of Schwann cell membrane, provides insulation for more efficient conduction of impulses.
Within cells, cholesterol is the precursor molecule in several biochemical pathways. In the liver, cholesterol is converted to bile, which is then stored in the gallbladder. Bile contains bile salts, which solubilize fats in the digestive tract and aid in the intestinal absorption of fat molecules as well as the fat-soluble vitamins, A, D, E, and K. Cholesterol is an important precursor molecule for the synthesis of vitamin D and the steroid hormones, including the adrenal gland hormones cortisol and aldosterone, as well as the sex hormones progesterone, estrogens, and testosterone, and their derivatives.
Some research indicates cholesterol may act as an antioxidant.
Dietary sources of Cholesterol
Animal fats are circuitous mixtures of triglycerides, with bottom amounts of phospholipids and cholesterol. As a consequence, all foods absolute beastly fat accommodate cholesterol to capricious extents. Major comestible sources of cholesterol cover cheese, egg yolks, beef, pork, poultry, fish, and shrimp. Human breast milk aswell contains cogent quantities of cholesterol.
From a comestible perspective, cholesterol is not begin in cogent amounts in bulb sources.In addition, bulb articles such as beat seeds and atom accommodate cholesterol-like compounds alleged phytosterols, which are believed to attempt with cholesterol for assimilation in the intestines. Phytosterols can be supplemented through the use of phytosterol-containing anatomic foods or nutraceuticals that are broadly accustomed as accepting a accurate LDL cholesterol-lowering efficacy. Current added guidelines acclaim doses of phytosterols in the 1.6-3.0 grams per day ambit (Health Canada, EFSA, ATP III,FDA) with a contempo meta-analysis demonstrating an 8.8% abridgement in LDL-cholesterol at a beggarly dosage of 2.15 gram per day. However, the allowances of a diet supplemented with phytosterol has been questioned.
Total fat assimilation aswell plays a role in claret cholesterol levels. This aftereffect is anticipation to appear about by changes in the abundance of cholesterol and lipoproteins that are actinic by the body. In particular, saturated, monounsaturated and polyunsaturated fats accept been apparent to access HDL-based cholesterol levels, with saturated fats aswell accretion LDL-based cholesterol levels. Trans fats accept been apparent to abate levels of HDL whilst accretion levels of LDL. Based on such affirmation and affirmation implicating low HDL and top LDL levels in cardiovascular ache (see Hypercholesterolemia), abounding bloom authorities apostle abbreviation LDL cholesterol through changes in diet in accession to added affairs modifications. The USDA for archetype recommends that those adulatory to abate their cholesterol through a change in diet should aim to absorb beneath than 7% of their circadian activity needs from saturated fat and beneath than 200 mg of cholesterol per day. An another appearance is that any abridgement to comestible cholesterol assimilation could be counteracted by the organs compensating to try to accumulate claret cholesterol levels constant.
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Monday, March 12, 2012

Applications of Tetrakis(triphenylphosphine)palladium(0)

Tetrakis(triphenylphosphine)palladium(0) is the chemical compound Pd[P(C6H5)3]4, often abbreviated Pd(PPh3)4, or even PdP4. It is a bright yellow crystalline solid that becomes brown upon decomposition in air.
Properties
The four P atoms are at the corners of a tetrahedron surrounding the palladium(0) center. This anatomy is archetypal for four-coordinate 18e complexes. The agnate complexes Ni(PPh3)4 and Pt(PPh3)4 are aswell able-bodied known. Such complexes reversibly abstract PPh3 ligands in solution, absolution the 16e M(PPh3)3. Thus, reactions attributed to Pd(PPh3)4 in actuality appear from Pd(PPh3)3 or even Pd(PPh3)2.
Applications
Tetrakis(triphenylphosphine)palladium(0) is broadly acclimated as a agitator for palladium-catalyzed coupling reactions. Prominent applications cover the Heck reaction, Suzuki coupling, Stille coupling, Sonogashira coupling, and Negishi coupling. These processes activate with two alternating ligand dissociations followed by the oxidative accession of an aryl halide to the Pd(0) center:Pd(PPh3)4 + ArBr → PdBr(Ar)(PPh3)2 + 2 PPh3
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Sunday, March 11, 2012

What is Iridium tetrachloride used for?

Iridium tetrachloride is an excellent water soluble crystalline Iridium source for uses compatible with chlorides. Chloride compounds can conduct electricity when fused or dissolved in water. Chloride materials can be decomposed by electrolysis to chlorine gas and the metal. They are formed through various chlorination processes whereby at least one chlorine anion (Cl-) is covalently bonded to the relevant metal or cation. Ultra high purity and proprietary formulations can be prepared. The chloride ion controls fluid equilibrium and pH levels in metabolic systems. They can form either inorganic or organic compounds.
Preparation
Iridium is afar from the added platinum accumulation metals as apparent ammonium hexachloroiridate(IV), (NH4)2[IrCl6] (CAS amount [16940-92-4]), which can be bargain to iridium metal in a beck of hydrogen. The absorptive Ir appropriately produced reacts with chlorine at 300–400 °C to aftermath iridium chloride. Like the accompanying rhodium compound, IrCl3 adopts the anatomy apparent for aluminium chloride.
The hydrated anatomy is acquired by heating hydrated iridium oxide with hydrochloric acid.
Uses of Iridium tetrachloride
Hydrated iridium chloride is acclimated in the class for the alertness of added iridium compounds such as Vaska's complex, trans-[IrCl(CO)(PPh3)2]. Alkene complexes such as the dimeric {Ir(COD)Cl}2[3], and {Ir(cycloctene)2Cl}2 can aswell be able by heating the trichloride with the adapted alkene in water/alcohol mixtures. Industrially, a lot of iridium complexes are generated from H2IrCl6 or (NH4)2IrCl6 as these salts are the a lot of accepted bartering forms of iridium chlorides, getting anon acquired in the ablution of iridium.
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Thursday, March 8, 2012

What is POTASSIUM DICYANOAURATE(I)?

POTASSIUM DICYANOAURATE(I)
Molecular Formula C2AuKN2
CAS No. 13967-50-5
Specific Gravity: 3.45 g/cm3
Solubility in H2O: Very soluble in H2O.
Appearance and Odor: White crystal powder, odor of almonds.
POTASSIUM is the actinic aspect with the attribute K (from Neo-Latin kalium) and diminutive amount 19. Elemental potassium is a bendable silvery-white acrid metal that oxidizes rapidly in air and is actual acknowledging with water, breeding acceptable calefaction to burn the hydrogen emitted in the reaction.
Potassium is an acutely alive metal, which reacts berserk with oxygen and baptize in air. With oxygen, it converts to potassium achromatize and with baptize potassium hydroxide. The acknowledgment of potassium with baptize is alarming because of its agitated exothermic appearance and the assembly of hydrogen gas. Hydrogen reacts afresh with atmospheric oxygen, bearing water, which reacts with the actual potassium. This acknowledgment requires alone traces of water; because of this, potassium and its aqueous admixture with sodium — NaK — are almighty desiccants that can be acclimated to dry solvents above-mentioned to distillation.
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Safety of CHLORO(TRIETHYLPHOSPHINE)GOLD(I)

Specifications of CHLORO(TRIETHYLPHOSPHINE)GOLD(I)
Offered as 250 mg (sc-227606)
CAS Number: 15529-90-5
Molecular Weight: 350.58
Molecular Formula: C6H15AuClP
Safety of CHLORO(TRIETHYLPHOSPHINE)GOLD(I)
Risk Statements: R23,R24,R25,R36,R37,R38
Safety Statements: S26,S28,S36,S37,S39,S45
assay 97%
bp 210 °C/0.03 mmHg(lit.)
mp 84-86 °C(lit.
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Wednesday, March 7, 2012

Properyies of Cholesteryl Acetate (Cholesterol acetate)

Cholesteryl Acetate (Cholesterol acetate)
Molecular Weight: 428.69
Molecular Formula: C29H48O2
Purity: ≥95%
Form: Solid
Physical Appearance: White crystalline powder
Solubility: Does not mix well with water. Soluble in chloroform.
Storage: Store at 4° C
Properties of Cholesteryl Acetate (Cholesterol acetate)
Boling Point: 493.3ºC
Boiling Point Pressure: 760 mmHg
Flash Point: 248.8ºC
Density: 0.99 g/cm3
Vapor Pressure: 7.13E-10 mmHg at 25ºC
Refractive Index: 1.515
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Uses of Dichlorotris(triphenylphosphine)ruthenium(II)

Dichlorotris(triphenylphosphine)ruthenium(II) is a allocation circuitous of ruthenium. This amber amber solid is a forerunner to added complexes including those acclimated as constant catalysis.
Properties
RuCl2(PPh3)3 is the artefact of the acknowledgment of ruthenium trichloride trihydrate with a methanolic band-aid of triphenylphosphine.
2 RuCl3(H2O)3 + 7 PPh3 → 2 RuCl2(PPh3)3 + 2 HCl + 5 H2O + 1 OPPh3
When conducted in the attendance of beyond balance of triphenylphosphine, the amalgam affords atramentous RuCl2(PPh3)4.
The allocation apple of RuCl2(PPh3)3 can be beheld as either five-coordinate or octahedral. One allocation website is active by one of the hydrogen atoms of a phenyl group. This Ru---H agostic alternation is continued (2.59 Å) and weak. The low agreement of the admixture is reflected by the differing lengths of the Ru-P bonds: 2.374, 2.412, and 2.230 Å. The Ru-Cl band lengths are both 2.387 Å.
Use
RuCl2(PPh3)3 facilitates oxidations, reductions, cross-couplings, cyclizations, and isomerization. It is acclimated in the Kharasch accession of chlorocarbons to alkenes.
Dichlorotris(triphenylphosphine)ruthenium(II) serves as a precatalyst for the hydrogenation of alkenes, nitro compounds, ketones, carboxylic acids, and imines. On the added hand, it catalyzes the blaze of alkanes to tertiary alcohols, amides to t-butyldioxyamides, and tertiary amines to α-(t-butyldioxyamides) application tert-butyl hydroperoxide. Application added peroxides, oxygen, and acetone, the agitator can burn alcohols to aldehydes or ketones. Application dichlorotris(triphenylphosphine)ruthenium(II) the N-alkylation of amines with alcohols is aswell accessible
RuCl2(PPh3)3 calmly catalyzes the atomization of formic acerbic into carbon dioxide and hydrogen gas in the attendance of an amine. Since carbon dioxide can be trapped and hydrogenated on an automated scale, formic acerbic represents a abeyant accumulator and busline medium.
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Monday, March 5, 2012

Where to buy TETRAKIS(TRIPHENYLPHOSPHINE)PLATINUM?

TETRAKIS(TRIPHENYLPHOSPHINE)PLATINUM is the chemical compound with the formula Pt(P(C6H5)3)4, often abbreviated Pt(PPh3)4. The bright yellow compound is widely used as a precursor to other platinum complexes.
The molecule is tetrahedral, with point group symmetry of Td, as expected for a four-coordinate metal complex of a metal with the d10 configuration. Even though this complex follows the 18 electron rule, it dissociates triphenylphosphine in solution to give the 16e− derivative containing only three PPh3 ligands: Pt(PPh3)4 → Pt(PPh3)3 + PPh3
The complex is typically prepared in one-pot reaction from potassium tetrachloroplatinate(II). Reduction of TETRAKIS(TRIPHENYLPHOSPHINE)PLATINUM with alkaline ethanol in the presence of excess triphenylphosphine affords the product as a precipitate. The reaction occurs in two distinct steps. In the first step, PtCl2(PPh3)2 is generated. In the second step, this platinum(II) complex is reduced. The overall synthesis can be summarized as:
K2[PtCl4] + 2KOH + 4PPh3 + C2H5OH → Pt(PPh3)4 + 4KCl + CH3CHO + 2H2O
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Sunday, March 4, 2012

Where to get Oxycarbonydichlorotris(triphenylphosphine)ruthenium?

Specifications of Oxycarbonydichlorotris(triphenylphosphine)ruthenium
Molecular Formula Ru(CO)2Cl2(PPh3)2
Synonyms Oxycarbonydichlorotris(triphenylphosphine)ruthenium
Dichlorotris(triphenylphosphine)ruthenium(II) is a coordination complex of ruthenium. This chocolate brown solid is a precursor to other complexes including those used as homogeneous catalysis.
Properties
Oxycarbonydichlorotris(triphenylphosphine)ruthenium is the product of the reaction of ruthenium trichloride trihydrate with a methanolic solution of triphenylphosphine.
When conducted in the presence of larger excess of triphenylphosphine, the synthesis affords black Oxycarbonydichlorotris(triphenylphosphine)ruthenium.
The coordination sphere of Oxycarbonydichlorotris(triphenylphosphine)ruthenium can be viewed as either five-coordinate or octahedral. One coordination site is occupied by one of the hydrogen atoms of a phenyl group. This Ru---H agostic interaction is long (2.59 Å) and weak. The low symmetry of the compound is reflected by the differing lengths of the Ru-P bonds: 2.374, 2.412, and 2.230 Å. The Ru-Cl bond lengths are both 2.387 Å.
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Thursday, March 1, 2012

Applications of PALLADIUM(II) NITRATE DIHYDRATE

PALLADIUM(II) NITRATE DIHYDRATE
Synonym: Palladium dinitrate hydrate
CAS Number: 313222-87-6
Molecular Weight: 248.45
Molecular Formula: N2PdO6 ·H2O
Physical Appearance: Powder
Application of PALLADIUM(II) NITRATE DIHYDRATE
Catalyst for alkene nitration to glycol dinitrates; also used as a precursor to supported Pd catalysts.
Reactant for
Preparation of platinum-palladium/carbon alloy nanocatalysts for methanol-tolerant oxygen reduction reaction in fuel cells
Synthesis of Cu-Pd alloy thin films on Ti substrates by co-electrodeposition of Pd and Cu from nitrate-base electrolytic baths
Preparation of palladium catalyst supported on vertically aligned multi-walled carbon nanotubes for microwave-assisted Heck reactions of p-iodonitrobenzene with styrene and Et acrylate
Preparation of a sinter-resistant Pd/SiO2 nanocatalyst
Preparation of di-phenyl sulfide-modified Pd/TiO2 catalysts for acetylene hydrogenation
Synthesis of alumina-supported palladium catalysts active for the gas phase hydrogenation of crotonaldehyde
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