warnernellのブログ -4ページ目

warnernellのブログ

ブログの説明を入力します。



Numerous PAHs have brought on tumors in laboratory animals that were confronted with PAHs by means of their food items, from breathing contaminated air and when it was utilized to their pores and skin. When pregnant mice ate large doses of the PAH (benzo(a)pyrene) they skilled reproductive issues. Besides, the offspring of the pregnant mice showed beginning defects and a reduce of their human body excess weight. Other consequences consist of injury to pores and skin, body fluids and also the immune program which will help the body battle condition. Yet, these consequences haven't been noticed in people.



Acenaphthene can bother your skin and mucous membranes. Animal studies showed that rats fed two grams of acenaphthene for 32 times (long time) had changes in their blood and some hurt on the liver, kidney and lungs.



There is no details accessible from research on humans to tell what outcomes can result from getting subjected to specific PAHs at specific ranges. However, respiration PAHs and pores and skin get in touch with seem to be associated with most cancers in human beings. Animal scientific studies showed that mice confronted with 308 elements for every million (ppm) of PAHs (specifically benzo(a)pyrene) in food for ten days (short-term coverage) had offspring with start defects. Mice subjected to 923 ppm of benzo(a)pyrene in foods for a period of months produced troubles inside the liver and blood.



Chemical Title:Acenaphthene

CAS: 83-32-9

Molecular Formulation: C12H10

Molecular Weight: 154.2078

Synonyms: 1,8-Ethylenenaphthalene;1,2-Dihydroacenaphthene;

EINECS: 201-469-6

Density: one.043 g/cm3

Melting Stage: 90-94 ??(lit.)

Boiling Level: 278.999 ?? at 760 mmHg

Flash Stage: 135.257 ??

Solubility: 0.000347 g/100 mL in h2o

Danger Codes: 36/37/38-50/53-39/23/24/25-23/24/25-11-52/53-67-65-38

Transportation: UN 3077 9/PG 3


You are able to be exposed to most PAHs inside the environment, in your home and in the workplace. Simply because PAHs exist obviously within the environment, and they are man-made, it is possible to be uncovered in the amount of approaches. Acenaphthene has become detected in fumes from automobile exhaust, coal, coal tar, and at hazardous throw away websites. These are all resources of coverage.



Because acenaphthene msds
has become present in cigarettes, you are able to be exposed by respiratory cigarette and tobacco smoke. Publicity to other PAHs can take place by taking in food items grown in contaminated soil or by eating meat or other food that you grilled. Grilling and charring foods in fact increases the number of PAHs in the foods.



If you function in a plant that makes coal-tar or that makes use of petroleum or coal, or helps make or makes use of wooden preservatives, you can be exposed to acenaphthene and other PAHs.



Chemical Title:Acenaphthene

CAS: 83-32-9


Molecular Formula: C12H10

Molecular Fat: 154.2078

Synonyms: one,8-Ethylenenaphthalene;1,2-Dihydroacenaphthene;

EINECS: 201-469-6

Density: 1.043 g/cm3

Melting Point: 90-94 ??(lit.)

Boiling Stage: 278.999 ?? at 760 mmHg

Flash Point: 135.257 ??

Solubility: 0.000347 g/100 mL in h2o

Risk Codes: 36/37/38-50/53-39/23/24/25-23/24/25-11-52/53-67-65-38

Transportation: UN 3077 9/PG 3
Chemical Title: Acenaphthene

cas 83-32-9

SMILES: c1cc2cccc3c2c(c1)CC3

Molecular Method:

Molecular Excess weight:

Synonyms: 1,8-Ethylenenaphthalene;1,2-Dihydroacenaphthene;

EINECS: 201-469-6

Density: one.043 g/cm3

Melting Position: 90-94 ??(lit.)

Boiling Point: 278.999 ?? at 760 mmHg

Flash Level: one hundred thirty five.257 ??

Solubility: 0.000347 g/100 mL in drinking water

Danger Codes: 36/37/38-50/53-39/23/24/25-23/24/25-11-52/53-67-65-38

Transportation: UN 3077 9/PG three



Acenaphthene is one of the group of chemicals called polycyclic aromatic hydrocarbons, PAHs for short. PAHs are often found collectively in sets of two or maybe more. They're able to exist in over 1 hundred different combinations but the most frequent are treated being a team of fifteen. PAHs are found naturally within the environment however they can be man-made. Acenaphthene appears just like a white crystal-like solid. PAHs are produced when goods like coal, oil, gasoline, and garbage are burned however the burning process just isn't full.





Extremely tiny details is offered to the person substances inside the PAH team. A lot of the info available is for the PAH team like a complete. Details precise to acenaphthene is included in this simple fact sheet when obtainable.

Amantadine was the first antiviral drugs used to inhibit the influenza virus, some anti-cold drugs containing amantadine. Amantadine in vivo metabolic degradation of a small amount, while the children's liver and kidney function is not fully developed, easy to accumulate in the body. Food and Drug Administration in order to ensure children's safe use of drugs, including the amantadine children cold medicine instructions to amend it. Amantadine-containing species involved include sunflower medicine Pediatric Paracetamol and Amantadine Hydrochloride Granules, Renhe Pharmaceutical excellent Cardin (Pediatric Paracetamol and Amantadine Hydrochloride particles), the crack of the Asian pharmaceutical capsules (Compound Paracetamol and Amantadine Hydrochloride Capsules the sun stone medicine doll (Pediatric paracetamol and Amantadine Hydrochloride granules), Hong Chi Pharmaceutical Jin Shuang ammonia Jin Huangmin particles). According to Statistics South, 2010, Compound Paracetamol and Amantadine drugs accounted for the cold medicine market share of 2.76%.Benefit most from treatment of cold medicine preparations.

The role of amantadine inhibition of influenza virus, the Food and Drug Administration and its restrictions on children's cold medicine, including of amantadine children cold medicine sales will affect. Treatment of cold medicine preparations by virtue of the safe, side effects, priority will benefit. The main benefit species listed companies including: the Hornsey pharmaceutical anti-viral oral liquid, China Resources Sanjiu 999 brand children Ganmaoling particles. 2011 anti-viral oral accounted for 58% of the Hornsey pharmaceutical revenue, the highest proportion in the listed companies.


Investment advice:To modify the instructions on non-prescription drugs containing amantadine, and other types of cold medicine, especially the sales of traditional Chinese medicine preparation. We believe that trading investment opportunities, it is recommended that concern the Hornsey pharmaceutical, China Resources Sanjiu anti-viral oral solution, taking into account a larger proportion of pharmaceutical revenues in Hornsey most Hornsey pharmaceutical.

Risk Warning:Adverse drug reactions: the excess of some drugs and inappropriate taking are likely to cause adverse reactions, leading to the regulatory agency restrictions on the scope of drug use.

White crystalline powder; soluble in organic solvents, insoluble in water; sublimation of sex, with the aromatic.
Chemical Name:ADAMANTANE
CAS: 281-23-2
Molecular Formula: C10H16
Molecular Weight: 136.23404
SMILES: C1C2CC3CC1CC(C2)C3
Synonyms: Tricyclo[3.3.1.13,7]decane;tricyclo[3.3.1.1(3,7)]decane;Adamantane (8CI);tricyclo[3.3.1.1~3,7~]decane;Tricyclo(3.3.1.13,7)decane;Tricyclo[3.3.1.13.7]decan-1-amine (Amantadine);
EINECS: 206-001-4
Density: 1.07g/mL, (20 °C)
Melting point :266-268 °C)
Storage Transport:The sealing of a cool, dry ventilated save
Appearance:
An alicyclic hydrocarbon, camphor-like odor. The molecular formula C10H16. Arrangement of carbon atoms in the molecule is equivalent to the part of the carbon atoms are arranged in the diamond lattice. Present in the oil content of about four millionths. Colorless crystals, its structure is highly symmetric molecules close to spherical, closely packed in the crystal lattice. The melting point of 268 ° C (sealed tube), alkanes, the relative density of 1.07. Likely to crystallize. Hydrogen on the bridgehead carbon atoms (ie, 1,3,5,7) is prone to substitution reactions. Such as adamantane and the excess bromine and generate 1 - bromo-adamantane; and nitrogen dioxide in the 175 ° C, the reaction to generate 1 - Polynitroadamantanes; 1 - Diamond alcohol with chromium trioxide and acetic acid oxidation to generate. Adamantane by the isomerization of the the tetrahydro dimerization of cyclopentadiene in the presence of anhydrous aluminum chloride obtained. Its derivatives can be used as drugs, such as 1 - amino-adamantane hydrochloride and 1 - adamantyl triethylamine hydrochloride can prevent influenza caused by A2 virus. There are two kinds of adamantane Chlorides.

Note: to be blunt with food or water, to reduce gastrointestinal irritation.

Adult usual dose of oral:
Antipyretic, analgesic, a 0.3-0.6g, 3 times a day, if necessary, every 4 hours 1.

Anti-rheumatic, day 3-5g (acute rheumatic fever can be used to 7 ~ 8g) orally 4 times.

Inhibition of platelet aggregation, there is no clear dosage, most advocate the application of small doses, such as 50-150mg every 24 hours.

Treatment of biliary ascariasis, a 1g, 2-3 times a day, once every 2-3 days; paroxysmal twist pain stop 24 hours after the disabled, and then de-worming treatment.

Pediatric usual dose of oral:
Antipyretic, analgesic, daily according to body surface area 1.5g / square meter, divided into 4 to 6 times a day orally, or each by 5-10mg/kg of weight or each 60mg per year-old, when necessary, 4 to 6 hours, 1 .
Anti-rheumatic, 80 ~ 100mg/kg of body weight daily, 3-4 times a service, such as 1-2 weeks without the efficacy, dosage can be adjusted under the plasma concentration. In some cases need to be increased to 130mg/kg daily.
Children used to mucocutaneous lymph node syndrome (Kawasaki disease), start daily by weight 80-100mg/kg, 3-4 times served hot back 2-3 days later changed to 30mg/kg a day divided into 2-4 during the times service, even service or more in February, thrombocytosis, blood hypercoagulable state, daily 5-10mg/kg, Dayton clothing.
Prevention of thrombosis, atherosclerosis and myocardial infarction: 0.3 / day; prevention of transient ischemic attack, 0.6g each time, 2 times a day.
Treatment of biliary ascariasis: each 1g, 2-3 times a day, even for 2-3 days.
Treatment of X-ray irradiation or radiotherapy-induced diarrhea, per serving, 0.6-0.9g, 4 times a day.
Tinea pedis rule, first with warm water or 1:5000 potassium permanganate solution, washed, and then the product powder spreading surface of the skin, usually 2-4 times more. Time to peak of salicylic acid in the morning administration long, long half-life of the evening the opposite. Reasonable administration of the morning dosage slightly increased. Night plus service time.

Usage of some diseases and the best dosage:
Systemic arterial embolism occurred in brain heart disease prevention valve alone, aspirin is invalid, but in combination with dipyridamole, will enhance the effect of small doses of dipyridamole.
Avoid and glucocorticoids in combination; avoid coumarin anticoagulant drugs, lowering blood sugar drug methotrexate, barbiturates, aniline and other combination.
After meals. American College of Chest Physicians Antithrombotic and Thrombolytic Therapy Association (ACCP) evidence-based guidelines state that the use of aspirin to prevent myocardial infarction, stroke and vascular death, the patient should be based on condition, the optimal dose.
A large number of clinical trials have shown that the majority of patients, including patients with chronic stable or unstable angina, aspirin 75mg / day can effectively reduce the risk of acute myocardial infarction and death. This dose can be reduced transient cerebral ischemic attack in patients with stroke and death incidence. Europe a stroke prevention studies have shown that a history of transient ischemic attack and stroke in patients with a history of aspirin 25mg, 2 times a day, 50mg / day can reduce the risk of stroke or death. Clinical Practice has proved that even in patients taking higher aspirin doses than the table, will not effect a further increase in the occurrence of side effects is greatly increased. Therefore, in the treatment of various thrombotic diseases, patients should use the smallest effective dose, ie, long-term application of 50-160mg / day, in order to achieve maximum efficacy, minimize side effects, this is the patients taking aspirin the optimal dose.
Analgesic, antipyretic: Aspirin through the expansion of blood vessels in the short run play to relieve headaches effects, the role of the drug on the dull than sharp pain. The drug can relieve mild or moderate dull pain such as headache, toothache, neuralgia, muscle pain and menstrual pain, and also used for colds, flu, fever. The goods can only relieve symptoms, not treat the cause pain, cause of fever, it takes the same time participate in treatment with other drugs. Anti-inflammatory, anti-rheumatic: Aspirin, the drug of choice for treatment of rheumatic fever, antipyretic medication can reduce inflammation, improvement in joint symptoms, erythrocyte sedimentation rate decreased, but not remove the basic pathology of rheumatoid changes, we can not prevent heart damage and other complications. If there has been significant myocarditis, are generally in favor of the first with adrenocorticotropic hormone, rheumatoid symptom control, disable hormones before, the product treatment, in order to reduce the rebound phenomenon caused by the disabled hormone. Arthritis: In addition to rheumatoid arthritis, the product is also used to treat rheumatoid arthritis can improve symptoms, to create conditions for further treatment. In addition, the product is used for osteoarthritis, ankylosing spondylitis, juvenile arthritis, and other non-rheumatic inflammation, musculoskeletal pain, can also relieve symptoms. Antithrombotic: The products on platelet aggregation inhibition, prevent thrombosis, the clinical can be used for the prevention of transient ischemic attack (TIA), myocardial infarction, atrial fibrillation, artificial heart valves, arteriovenous fistula or other of the post-operative thrombosis formation. Also be used for the treatment of unstable angina. Skin and mucous membrane lymph node syndrome: Of aspirin in children suffering from Kawasaki disease, the aim is to reduce the inflammatory response and the prevention of intravascular thrombus formation. Prevention of gastrointestinal tumors: The long-term regular use of aspirin can significantly reduce the incidence of tumors of the gastrointestinal tract.

As early as 1853 Charles Gerhardt, salicylic acid and acetic anhydride synthesized acetylsalicylic acid, but no attention has been paid; 1898 German chemist Feihuofuman, synthetic, and for his father to treat rheumatism arthritis, excellent efficacy; 1899 by Theodore Dreiser introduced into clinical, and named aspirin. So far, aspirin has been applied a century, the medical history of the three classic one of the drugs, it still is the world's most widely used antipyretic, analgesic and anti-inflammatory drugs, but also as a comparison and evaluation of other drugs Standard preparations. Antithrombotic effect in vivo, can inhibit the platelet release reaction, inhibition of platelet aggregation, reduction of TXA2 generated. Clinically used to prevent the onset of cardiovascular and cerebrovascular diseases.

Aspirin in the 1898 listing, in recent years it also has the role of anti-platelet aggregation, and so re-aroused great interest. Aspirin and other salicylic acid derivatives and polyvinyl alcohol, cellulose acetate, etc. Containing Hydroxyl polymer melt esterification, its polymer, the resulting product of anti-inflammatory and antipyretic analgesics than free A aspirin is more long-lasting.

According to literature, said the inventor of aspirin was Felix Hoffman of Germany, but this invention, plays a very important role in a Jewish chemist Arthur Ai Xing Green. Artur Ai Xing Green's bitter story takes place in 1934-1949. In 1934, Felix Hoffman claimed that he invented aspirin. Then Germany is in the dark period of Nazi persecution of Jews intensified. In this case, the arrogant Nazi rulers more reluctant to recognize the inventor of aspirin in the fact that the Jews, so they would be wrong to wear the crown of the inventor Felix Hoffmann, a person's head. "Germanic racial superiority theory" laced with gold. Nazi rulers in order to block the mouth of Artur Ai Xing Green, also put into a concentration camp. After World War II, about 1949, Artur Ai Xing Green raised this issue, but he soon died. Since then, this matter will go down the drain. British physician, historian Walter Snyder twists and turns to get the license of Bayer AG, Germany, access to all files in the Bayer laboratory, and finally restore the hard facts of the history of the true face of this invention. He pointed out: the invention of aspirin, Artur Ai Xing Green contributed. The fact is that in 1897, Felix Hoffman is indeed the first synthesized the main substances constitute aspirin, but he is under the guidance of his superiors - the well-known chemist Arthur Ai Xing Green and completely Ai Xing Green technology routes only to be successful.

Aspirin is a long history of antipyretic analgesics, was born March 6, 1899. Used to treat colds, fever, headache, toothache, joint pain, rheumatism, can inhibit platelet aggregation, surgery for the prevention and treatment of ischemic heart disease, angina, heart and lung infarction, cerebral thrombosis, used in blood vessel formation and bypass grafting.

Chemical Name: ASPIRIN
CAS: 50-78-2
SMILES: CC(=O)Oc1ccccc1C(=O)O
Molecular Formula: C9H8O4
Molecular Weight: 180.15742
Synonyms: Rhodine(7CI);Salicylic acid acetate (8CI);2-(Acetyloxy)benzoic acid;AC 5230;Acetophen;Acetysal;Acimetten;Acisal;Saletin;Solpyron;Supac;Temperal;Toldex;Trombyl;Yasta;o-(Acetyloxy)benzoic acid;Acetyl Salicylic Acid;Adiro;Asaflow;Asagran;Asatard;Ascoden 30;Ascriptin;Aspalon;Aspirdrops;Aspirin;Aspirin Protect 300;Aspirin-Direkt;Aspro;Aspropharm;Astrix;Benaspir;Bialpirinia;Caprin;Coricidin D;Dolean pH 8;Easprin;Ecotrin;Endosprin;Entericin;Ewin;Extren;Gelprin;
EINECS: 200-064-1
Density: 1.35
Melting Point: 134-136 ℃(lit.)
Boiling Point: 321.4 ℃ at 760 mmHg
Flash Point: 131.1 ℃
Solubility: water: 3.3 g/L (20 ℃)
Risk Codes: 22-36/37/38
Transportation: UN 1851

Nature Description: white needle-like or platy crystal or powder. The melting point of 135 ~ 140 ℃. Odorless, microstrip sour. Stable in dry air, slowly hydrolyze into salicylic acid and acetic acid in moist air. Soluble in ethanol, dissolved in ether and chloroform, slightly soluble in water, can be dissolved in sodium hydroxide solution or sodium carbonate solution, but at the same decomposition. The product 1g can be dissolved in 300ml water 5ml alcohol 10-15ml ether and 17ml chloroform.

Safety Instructions: S26: In case of contact with eyes, rinse immediately with plenty of water and hospital treatment; S36/37/39: Wear suitable protective clothing, gloves and protective glasses or face shields.
Hazard Symbols: Xn: harmful substances
Risk Codes: R22: Harmful if swallowed; R36/37/38: have a stimulating effect on the eyes, respiratory tract and skin.
Transport of Dangerous Goods Number: UN1851
Application: application of the earliest and most widely used and most common antipyretic analgesic anti-rheumatic drug. Has antipyretic, analgesic, anti-rheumatic and anti-platelet aggregation, and many other pharmacological effects, play the rapid efficacy, efficacy and stability, ultra-dose easy to diagnosis and treatment, and rarely allergic reactions. Commonly used in cold and fever, headache, neuralgia, joint pain, muscle pain, rheumatic fever, acute within the wet arthritis, rheumatoid arthritis and toothache. "National Essential Drugs List" included in the varieties of acetylsalicylic acid is the other drug intermediates.
Production methods: Salicylic acid acetylation derived: acetic anhydride (the feedstock in the reaction tank to 0.7889 times the total amount of salicylate), then add two-thirds of the amount of salicylic acid, and stir to heat up in the 81-82 ℃ reaction of 40-60min. Cooling to 81-82 ° C insulation reaction 2h. Check for free salicylic acid after passing, cooling to 13 ° C, precipitation crystallization, rejection filter, washing drying, air drying at 65-70 ° C, acetyl salicylic acid.

The so-called pharmaceutical intermediates, in fact, for drug synthesis process in a number of chemical raw materials or chemical products. This chemical products, does not require drug production licenses in the ordinary chemical plant can produce some level, can be used for the synthesis of pharmaceuticals.

China's beta-lactam antibiotics after nearly 50 years of development, has formed a complete production system. Almost all beta-lactam antibiotics (except for the patent period of the species) in China can produce low cost, penicillin production in the world's top export supply the international market; the cephalosporins basic self-sufficient, can buy part of exports.
Intermediates in China, and beta-lactam antibiotics, supporting all be able to produce their own, in addition to semi-synthetic antibiotic nucleus 7-ACA and 7-ADCA need some imported, all of the side chain intermediates can be produced, and a large number of exports.
The main supporting intermediate phenylacetic acid to beta-lactam antibiotics, for example, our existing manufacturers phenylacetate 30, with a total production capacity of about 20,000 tons. But the small scale of most enterprises, the largest annual output of 2000 tons, most other annual output of hundreds of tons. Domestic the phenylacetate total demand in 2003 is about 1.4 million tons, the consumption structure as follows: penicillin G accounted for 85%, other medical (4%), spices (7%), pesticides and other areas accounted for 4%.
With the development of domestic spices, medicine, pesticide and other industries, acid demand will increase further. Expected in 2005, China's pharmaceutical industry will consume about 14,000 tons of phenylacetic acid, the pesticide industry will consume 500 tons, the spice industry consumption of about 2000 tons. Plus other areas of consumption, expected domestic phenylacetate total demand will reach 18,000 tons in 2005.

At present, China has developed and put into mass production quinolones norfloxacin, ciprofloxacin, ofloxacin, enoxacin, lomefloxacin, fleroxacin magnitude. Including norfloxacin, ciprofloxacin, ofloxacin, producing the largest amount, 98% of the total output of accounting for the fluoroquinolone antibacterial drug.
The quinolones general condensation with piperazine (or piperazine) derived from fluorine-containing benzene ring synthesis of fluorinated quinoline compounds. Abundant fluorite reserves in China, which is one of the largest countries of the fluorine-containing drugs and intermediates production, there are more than 80% of the fluorine-containing intermediates for export. Overall, the development of fluorobenzene intermediates in China earlier, the current production capacity is generally excess; the benzotrifluoride class intermediate development of late, with fast development in recent years; and heterocyclic aromatic compounds, especially fluorinated pyridine class, our present, only the individual research institutes and manufacturers with the synthesis of fluorinated pyridines intermediates, fluorine-containing pyridine intermediates will become one of the main directions of domestic fluorine-containing intermediates, R & D in the next few years.

China has become the world's largest production of the antipyretic analgesics, aspirin, paracetamol, dipyrone and other varieties yield surpassed tons, non-phenacetin, aminopyrine, security for more than forests and other species of output over 1000 tons. Of antipyretic analgesics output growth is expected that the future will increase rate of about 8%. Antipyretic analgesics supporting the production of intermediates production, and production enterprises. With the growth of antipyretic analgesics, and its intermediates has also received considerable development.
Domestic paracetamol consumption in 2003 a rapid increase in exports also showed a rapid growth, the export volume of 28,163 tons, an increase of annual export volume amounted to about 1 times. The first half of 2004, its export growth slowed, but still an increase, 2004 to May paracetamol exports of 12,501 tons, slightly higher than the same period last year. The aminophenol important intermediates for the synthesis of paracetamol in recent years, rapid growth. At present, China's annual production of aminophenol is about 32,000 tons, is expected to 2005, domestic paracetamol production will reach more than 50,000 tons, the pharmaceutical industry will consume 45,000 tons aminophenol, coupled with the application in other fields, 2005 aminophenol total demand of about 50,000 tons, a larger gap in the market, development and utilization of broad prospects.

Throughout the industry, the production of pharmaceutical intermediates in China has six characteristics: First, the production enterprises to the private sector, operating flexibility, and investment in small, basically a few million to 20 million yuan; manufacturers The geographical distribution is relatively concentrated, mainly located in Taizhou, Zhejiang and Jiangsujintan areas; Third, as the country's increasing emphasis on environmental issues, environmental treatment facilities for production enterprises to build pressure increases; four product updates faster. A product is generally 3 to 5 years after the market, its profit margin dropped significantly, forcing companies must constantly develop new products and continuously improving production process in order to maintain high production and profits; five is due to the production of pharmaceutical intermediates, high-profit chemical products, both the production process is basically the same, so there will be a growing number of small chemical companies joined the ranks of the production of pharmaceutical intermediates, leading to the disorder in an increasingly competitive industry; six, compared with the raw material drug production intermediate low profit margins, pharmaceutical raw materials and the production of pharmaceutical intermediates, and a result, some enterprises have not only the production of intermediates, and also use their own advantage, and began producing bulk drugs.