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リンダン

リンダン 化学構造式
58-89-9
  • CAS番号.58-89-9
  • 化学名:リンダン
  • 别名:1,2,3,4,5,6-ヘキサクロロシクロヘキサン (γ-異性体);ゲキサン;ガンマ-BHC;リンダトクス;ベンゼンヘキサクロリド;ロレキサン;アグロシド;γ-リンダン;ガンマ-HCH;1α,2α,3β,4α,5α,6β-ヘキサクロロシクロヘキサン;リンダン;クウェル;リンデン;ヘキサクロロシクロヘキサン;γ-ヘキサクロロシクロヘキサン;ヘキサクロラン;Γ-BHC標準品;Γ-HCH標準品;Γ-HCH標準液 CRM4203-A;γヘキサクロロシクロヘキサン
  • 英語化学名:LINDANE
  • 英語别名:666;BBH;HGI;plk;HCH;HCCH;G-BHC;D-BHC;D-HCH;Kwell
  • CBNumber:CB5281877
  • Molecular Formula:C6H6Cl6
  • Formula Weight:290.81
  • MOL File:58-89-9.mol
リンダン 物理性質
  • 融点  :113-115 °C(lit.)
  • 沸点  :373.64°C (rough estimate)
  • 比重(密度)  :1.7152 (rough estimate)
  • 蒸気圧 :28.0, 55.3, 87.0, 168.8, 285.8, 297.0, and 538.5 at 19.58, 24.95, 28.42, 33.58, 37.82, 37.86, and43.32 °C, respectively (Boehncke et al., 1996)
  • 屈折率  :nD20 1.644
  • 闪点  :11 °C
  • 貯蔵温度  : 0-6°C
  • 溶解性 :H2O: insoluble0.01g/L (practically)
  • 水溶解度  :7.3 mg l-1 (25 °C)
  • 外見  :neat
  • Merck  :13,5523
  • BRN  :1907337
  • Henry's Law Constant :12.8 at 5 °C, 14.8 at 15 °C, 18.8 at 20 °C, 26.6 at 25 °C, 38.5 at 35 °C (gas stripping-GC, Cetin et al., 2006)
  • 暴露限界値 :NIOSH REL: TWA 0.5 mg/m3, IDLH 50 mg/m3; OSHA PEL: TWA 0.5 mg/m3; ACGIH TLV: TWA 0.5 mg/m3.
  • 安定性: :Stable. Incompatible with strong oxidizing agents.
  • NISTの化学物質情報 :Lindane(58-89-9)
  • IARC :1 (Vol. 113) 2018
  • EPAの化学物質情報 :Lindane (58-89-9)
安全性情報
危険有害性情報のコード(GHS)
  • 絵表示(GHS)
  • 注意喚起語Danger
  • 危険有害性情報
  • H225:引火性の高い液体および蒸気
  • H301:飲み込むと有毒
  • H304:飲み込んで気道に侵入すると生命に危険のおそ れ
  • H315:皮膚刺激
  • H336:眠気やめまいのおそれ
  • H362:授乳中の子に害を及ぼすおそれ
  • H370:臓器の障害
  • H373:長期にわたる、または反復暴露により臓器の障 害のおそれ
  • H410:長期的影響により水生生物に非常に強い毒性
  • H412:長期的影響により水生生物に有害
  • 注意書き
  • P201:使用前に取扱説明書を入手すること。
  • P210:熱/火花/裸火/高温のもののような着火源から遠ざ けること。-禁煙。
  • P260:粉じん/煙/ガス/ミスト/蒸気/スプレーを吸入しないこ と。
  • P263:妊娠中/授乳期中は接触を避けること。
  • P273:環境への放出を避けること。
  • P280:保護手袋/保護衣/保護眼鏡/保護面を着用するこ と。
  • P301+P310:飲み込んだ場合:直ちに医師に連絡すること。
  • P331:無理に吐かせないこと。
  • P391:漏出物を回収すること。
  • P403+P233:換気の良い場所で保管すること。容器を密閉 しておくこと。
  • P501:内容物/容器を...に廃棄すること。
リンダン 価格 もっと(28)
  • メーカー: 富士フイルム和光純薬株式会社(wako)
  • 製品番号: W01ACSAPP-9-025
  • 製品説明 : リンデン Standard
  • 純度: Lindane Standard, 100 ug/mL in MeOH
  • 包装: 1mL
  • 価格: ¥4400
  • 更新時間: 2021/03/23
  • 購入: 購入
  • メーカー: 富士フイルム和光純薬株式会社(wako)
  • 製品番号: W01ACSAS-E0102
  • 製品説明 : γ-BHC BHCndリンデンandard
  • 純度: gamma-BHC (Lindane) Standard, 1000 ug/mL in MeOH
  • 包装: 1mL
  • 価格: ¥11800
  • 更新時間: 2021/03/23
  • 購入: 購入
  • メーカー: 東京化成工業
  • 製品番号: H0056
  • 製品説明 : 1,2,3,4,5,6-ヘキサクロロシクロヘキサン (γ-異性体)
  • 純度: 1,2,3,4,5,6-Hexachlorocyclohexane (γ-Isomer) >99.0%(GC)
  • 包装: 5g
  • 価格: ¥2000
  • 更新時間: 2021/03/23
  • 購入: 購入
  • メーカー: 東京化成工業
  • 製品番号: H0056
  • 製品説明 : 1,2,3,4,5,6-ヘキサクロロシクロヘキサン (γ-異性体)
  • 純度: 1,2,3,4,5,6-Hexachlorocyclohexane (γ-Isomer) >99.0%(GC)
  • 包装: 25g
  • 価格: ¥3500
  • 更新時間: 2021/03/23
  • 購入: 購入
  • メーカー: 関東化学株式会社(KANTO)
  • 製品番号: 49802-35
  • 製品説明 : γ‐HCH標準品
  • 純度: γ‐HCH standard
  • 包装: 250mg
  • 価格: ¥13000
  • 更新時間: 2021/03/23
  • 購入: 購入

LINDANE 化学特性,用途語,生産方法

  • 外観 白色, 結晶~粉末
  • 溶解性 水に難溶。多くの有機溶媒に可溶。石油系の溶媒には微溶。水7.3(25℃), 12 (35℃) いずれもmg/l。アセトン43.5, メタノール7.4, エタノール6.4, ベンゼン28.9, トルエン27.6, キシレン24.7, ジエチルエーテル20.8, 石油エーテル2.9, 酢酸エチル35.7, クロロホルム24.0, 四塩化炭素6.7, シクロヘキサン36.7, ジオキサン, 31.4, 酢酸12アセトンにやや溶けやすく、エタノールに溶けにくく、水にほとんど溶けない。
  • 用途 殺虫剤(販売禁止農薬) (NITE CHRIP)
  • 効能 殺シラミ薬, 殺疥癬虫薬
  • 農薬用途 殺虫剤
  • 説明 Lindane is one of eight different hexachlorocyclohexane (HCH), [58-89-9], C6H6Cl6, isomers and its Chemical Abstract name is 1α, 2α,3β,4α,5α,6β- hexachlorocyclohexane 58-89-9 (γ-HCH or γ -BHC, benzene hexachloride) (80). Commercial products containing lindane are marketed as either a mixture of isomers or as the pure γ -BHC isomer. Not unexpectedly, lindane is a highly stable lipophilic compound and it has been used extensively worldwide as an insecticide. In contrast, hexachloropentadiene, [77-47-4], C5Cl6, is an extremely reactive industrial intermediate used as a chemical intermediate in the synthesis of a broad range of cyclodiene-derived pesticides, which include endosulfan, endrin, heptachlor, and several different organohalogen flame retardants (81).
  • 化学的特性 white powder
  • 化学的特性 Lindane is a white to yellow, crystalline powder with a slight, musty odor (pure material is odorless).
  • 化学的特性 BHC is a white-to-brownish crystalline solid with a musty, phosgene-like odor.
  • 物理的性質 Colorless to yellow crystalline solid with a slight, musty, chlorinated-like odor. Odor threshold concentration is 12.0 mg/kg (Sigworth, 1964). Robeck et al. (1965) reported an odor threshold of 330 ppb.
  • Originator Kwell,Reed Carnrick,US,1952
  • 使用 Pesticide and insecticide.
  • 使用 The only identified uses for hexachlorocyclohexane-containing products are based on the insecticidal activity of the γ isomer (lindane), which is considered to be the only insecticidally effective component (Extoxnet 1996). Lindane or technical-grade hexachlorocyclohexane containing the γ isomer is used primarily as an insecticide in the treatment of wood and wooden structures, seed grains, and livestock (ATSDR 2005, HSDB 2009). Other major uses are as an insecticide for several dozen fruit and vegetable crops, in baits and seed treatments for rodent control, and for treatment of scabies (mites) and lice. It is approved by the U.S. Food and Drug Administration foruse in three products for the treatment of lice and scabies (one lotionand two shampoos) (FDA 2009). Agricultural and pesticide uses accounted for about 270,000 kg (594,000 lb) of lindane and 450,000 kg (1 million pounds) of technical-grade hexachlorocyclohexane in 1974;the remaining uses were industrial or pharmaceutical (IARC 1979).
  • 使用 Insecticide.
  • 適応症 Lindane (Gamma benzene hexachloride, Kwell, Thionex) is a cyclic chlorinated hydrocarbon originally developed as an agricultural insecticide. It is absorbed through the chitinous exoskeleton and stimulates the nervous system, resulting in seizures and death of the insect. It is both a pediculicide and scabicide, with a 45% to 70% ovicidal effect. Resistance has been shown to Pediculosis capitis and Sarcoptes scabiei.
    Lindane can be absorbed through intact skin following topical application and has the potential for CNS toxicity. It should therefore be used with great caution in infants, children <2 years of age, elderly patients, and pregnant and lactating women. It may be irritating to the eyes or mucous membranes; hence, these areas should be avoided. Irritant dermatitis may occur with use of excessive amounts or over prolonged periods. Toxicity, if overused, may result in nausea, vomiting, seizures, or even bone marrow suppression.
    Lindane is an organochlorine with very slow onset of action and poor ovicidal activity; it takes over 3 hours to kill the lice during which increased lice crawling and twitching can cause increased pruritus for the patient. Lindane is available as a shampoo for the treatment of pediculosis capitis and/or pubis and in cream and lotion form for treating scabies and all forms of pediculosis. GBH also repels ticks and other arthropods and kills chiggers.
  • Manufacturing Process Chlorine gas was gradually passed into 660 parts of benzene contained in a lead-lined reaction vessel until 890 parts of the gas had been absorbed. The mixture was stirred continuously and the temperature maintained at 15°C to 20°C.
    The supply of chlorine was then interrupted and the precipitated solid filtered off and dried. In weight, it was found to be equivalent to 900 parts. The mother liquid was then mixed with 330 parts of benzene and the mixture again treated with 890 parts of chlorine in the manner described.
    After filtering the reaction mixture resulting from the second chlorination, the filtrate was again mixed with a smaller quantity of benzene and again chlorinated in a similar manner. In this way, a continuous process for the preparation of benzene hexachloride resulted.
    That benzene hexachloride isomer mixture is then the raw material for lindane production. The production of lindane per se is not a chemical synthesis operation but a physical separation process. It is possible to influence the gamma isomer content of benzene hexachloride to an extent during the synthesis process. Basically, however, one is faced with the problem of separating a 99%-plus purity gamma isomer from a crude product containing perhaps 12 to 15% of the gamma isomer. The separation and concentration process is done by a carefully controlled solvent extraction and crystallization process. One such process is described by R.D. Donaldson et al. Another description of hexachlorocyclohexane isomer separation is given by R.H. Kimball.
  • brand name Benhexachlor;Gamex;Gamma benzene;Hexachloride.
  • Therapeutic Function Pediculicide, Scabicide
  • 世界保健機関(WHO) Lindane has been available for more than 25 years and is widely used as an agricultural and household pesticide.
  • 一般的な説明 Colorless solid with a musty odor; pure material is odorless. Used as a pesticide and scabicide.
  • 空気と水の反応 Insoluble in water.
  • 反応プロフィール LINDANE is incompatible with strong bases. LINDANE is incompatible with powdered metals such as iron, zinc and aluminum. LINDANE is also incompatible with oxidizing agents. LINDANE can undergo oxidation when in contact with ozone. When exposed to alkalis, LINDANE undergoes dehydrochlorination.
  • 健康ハザード LINDANE is a stimulant of the nervous system, causing violent convulsions that are rapid in onset and generally followed by death or recovery within 24 hours. The probable human oral lethal dose is 50-500 mg/kg, or between 1 teaspoon and 1 ounce for a 150-lb (70 kg) person.
  • 健康ハザード High acute toxicity; symptoms — headache,dizziness, nausea, vomiting, diarrhea, tremor,cyanosis, epileptic convulsions; stimulant tonervous system, which can lead to violent convulsions; such convulsions may setrapidly that may either progress to recovery within 24 hours or could lead to death(Hayes 1982); ingestion of 2–10 g probably fatal to human; an irritant to eyeand skin; chronic exposure causes liverinjury; oral LD50 value (mice): 86 mg/kg;carcinogenic to animals, causing liver andlung tumors; exposure limit: TLV : TWA(skin) 0.5 mg/m3 (ACGIH, MSHA, andOSHA); RCRA Waste Number U120.
  • 火災危険 When heated to decomposition, LINDANE emits toxic fumes of chlorine, hydrochloric acid, and phosgene.
  • 农业用途 Insecticide, Rodenticide: Lindane has been used against insects in a wide range of applications including treatment of animals, buildings, man for ectoparasites, clothes, water for mosquitoes, living plants, seeds and soils. Most applications have been canceled due to excessive residues, e.g., stored foodstuffs, that may cause cancer. Formulators, distributors and users of lindane represent a special risk group. The major use of lindane in recent years has been to pretreat seeds. Other uses include sunflowers, peas, wheat, barley and oats. Lindane is currently also used in lotions, creams and shampoos for the control of lice and mites in humans. Not approved for use in EU countries. A U.S. EPA restricted Use Pesticide (RUP). Lindane should be handled as a carcinogen, with extreme caution. Most applications have been canceled. It has not been produced in the U.S. since 1977; however, it is still imported into the U.S. and formulated to treat head lice, body lice and scabies.
  • 製品名 AALINDAN®; AFICIDE®; AGRISOL G-20®; AGROCIDE®; AGRONEXIT®; AMEISENATOD®; AMEISENMITTEL (MERCK)®; APARASIN®; APHTIRIA®; APLIDAL®; ARBITEX®; BEN-HEX®; BENTOX 10®; CELANEX®; CHLORESENE®; CODECHINE®; DELSANEX DAIRY FLY SPRAY®; DETMOL-EXTRAKT®; DETOX 25®; DEVORAN®; DOL GRANULE®; DRILL TOXSPEZIAL AGLUKON®; DUAL MURGANIC RPB SEED TREATMENT®; ENTOMOXAN®; EXAGAMA®; FORLIN®; GALLOGAMA®; GAMACID®; GAMAPHEX®; GAMENE®; GAMMA-COL®; GAMMALIN®; GAMMALIN 20; GAMMALEX®; GAMMASAN 30®; GAMMATERR®; GAMMAPHEX®; GAMMEX®; GAMMEXANE®; GAMMEXENE®; GAMMOPAZ®; GEXANE®; HECLOTOX®; HEXA®; HEXAFLOW®; HEXATOX®; HEXAVERM®; HEXICIDE®; HEXYCLAN®; HORTEX®; INEXIT®; ISOTOX®; JACUTIN®; KOKOTINE®; KWELL®; LENTOX®; LINDAGRAM®; LIDENAL®; LINDAFOR®; LINDAGAM®; LINDAGRAIN®; LINDAGRANOX®; LINDAPOUDRE®; LINDATOX®; LINDOSEP®; LINTOX®; LOREXANE®; MARSTAN FLY SPRAY®; MERGAMMA 30®; MILBOL 49®; MIST-O-MATIC LINDEX®; MSZYCOL®; NEXEN FB®; NEXIT®; NEXIT-STARK®; NEXOL-E®; NICOCHLORAN®; NOVIGAM®; OMNITOX®; OVADZIAK®; OWADZIAK®; PEDRACZAK®; PFLANZOL®; QUELLADA®; RODESCO INSECT POWDER®; SANG GAMMA®; SILVANO®; SPRITZ-RAPIDIN®; SPRUEHPFLANZOL®; STREUNEX®; TAP 85®; TRI- 6®; VITON®
  • 接触アレルゲン Lindane is a pesticide used for its antiinsect properties in agriculture, wood protection, in antiinsect paints and veterinary and human medicine against many and veterinary and human medicine against many and demodicidosis. Its use is controlled, particularlybecause of neurological toxicity
  • 臨床応用 Lindane is 1,2,3,4,5,6-hexachlorocyclohexane, -benzenehexachloride, or benzene hexachloride (Kwell, Scabene,Kwildane, G-Well). This halogenated hydrocarbon is preparedby the chlorination of benzene. A mixture of isomersis obtained in this process, five of which have been isolated:α, β, γ, δ, and ε. The γ-isomer, present to 10% to 13% inthe mixture, is responsible for the insecticidal activity. The -isomer may be separated by various extraction and chromatographictechniques.Lindane occurs as a light buff to tan powder with a persistentmusty odor, and it is bitter. It is insoluble in water butsoluble in most organic solvents. It is stable under acidic orneutral conditions but undergoes elimination reactions underalkaline conditions.The action of lindane against insects is threefold: it is a directcontact poison, it has a fumigant effect, and it acts as astomach poison. The effect of lindane on insects is similar tothat of DDT. Its toxicity in humans is somewhat lower thanthat of DDT. Because of its lipid solubility properties, however,lindane when ingested tends to accumulate in the body.Lindane is used locally as a cream, lotion, or shampoo forthe treatment of scabies and pediculosis.
  • 安全性プロファイル Confirmed carcinogen with experimental carcinogenic and neoplastigenic data. A human systemic poison by ingestion. Also a poison by ingestion, skin contact, intraperitoneal, intravenous, and intramuscular routes. Human systemic effects by ingestion: convulsions, dyspnea, and cyanosis. Experimental teratogenic and reproductive effects. Mutation data reported. See also BENZENE HEXACHLORIDE and other benzene hexachloride entries. When heated to decomposition it emits toxic fumes of Cl-, HCl, and phosgene.
  • 職業ばく露 The major commercial usage of BHC is based upon its insecticidal properties. α-BCH is used as an Agricultural chemical, pesticide, pharmaceutical, and veterinary drug. The 7-isomer has the highest acute toxic ity, but the other isomers are not without activity. It is gen erally advantageous to purify the 7-isomer from the less active isomers. The γ-isomer acts on the nervous system of insects, principally at the level of the nerve ganglia. As a result, lindane has been used against insects in a wide range of applications including treatment of animals, buildings, humans for ectoparasites, clothes; water for mosquitoes; living plants; seeds and soils. Some applications have been abandoned due to excessive residues, e.g., stored food stuffs. By voluntary action, the principal domestic producer of technical grade BHC requested cancellation of its BHC registrations on September 1, 1976. As of July 21, 1978, all registrants of pesticide products containing BHC voluntar ily canceled their registrations or switched their former BHC products to lindane formulations.
  • Carcinogenicity Lindane (as γ-hexachlorocyclohexane), hexachlorocyclohexan e (technical grade), and other hexachlorocyclohexane isomers are reasonably anticipated to be human carcinogens based on sufficient evidence of carcinogenicity from studies in experimental animals.
  • 環境運命予測 Biological. In a laboratory experiment, a strain of Pseudomonas putida culture transformed lindane to g-3,4,5,6-tetrachlorocyclohexane (g-TCCH), g-pentachlorocyclohexane (g-PCCH) and a-BHC (Benezet and Matsumura, 1973). g-TCCH was also reported as a product of lindane degradation by Clostridium sphenoides (MacRae et al., 1969; Heritage and MacRae, 1977, 1977a), an anaerobic bacterium isolated from flooded soils (MacRae et al., 1969; Sethunathan and Yoshida, 1973a). Lindane degradation by Escherichia coli also yielded g-PCCH (Francis et al., 1975). Evidence suggests that degradation of lindane in anaerobic cultures or flooded soils amended with lindane occurs via reductive dehalogenation producing chlorine-free volatile metabolites (Sethunathan and Yoshida, 1973a).
    After a 30-day incubation period, the white rot fungus Phanerochaete chrysosporium converted lindane to carbon dioxide. Mineralization began between the third and sixth day of incubation. The production of carbon dioxide was highest between 3 to 18 days o
    Beland et al. (1976) studied the degradation of lindane in sewage sludge under anaerobic conditions. Lindane underwent reductive hydrodechlorination forming 3,4,5,6-tetrachlorocyclohex- 1-ene (g-BTC). The amount of g-BTC that formed reached a maximum conc
    When lindane was incubated in aerobic and anaerobic soil suspensions for 3 weeks, 0 and 63.8% was lost, respectively (MacRae et al., 1984). Using settled domestic wastewater inoculum, lindane (5 and 10 mg/L) did not degrade after 28 days of incubation at 25°C (Tabak et al., 1981).
    Soil. In moist soils, lindane biodegraded to g-pentachlorocyclohexene (Elsner et al., 1972; Kearney and Kaufman, 1976; Fuhremann and Lichtenstein, 1980). Under anaerobic conditions, degradation by soil bacteria yielded g-BTC and a-BHC (Kobayashi
  • 代謝経路 The metabolic pathways of gamma-HCH are complex and more than 80 metabolites have been identified (Macholz and Kujawa, 1985). Dehydrohalogenation reactions are important. Gamma-HCH may be converted into other HCH isomers in the environment and also microorganisms and plants may convert gamma-HCH (1) into the alpha (2), beta (3), or delta (4) isomers (see Schemel). Bioisomerisation does not appear to be a significant pathway in mammals. In animals, metabolism of gamma-HCH generally leads to less-chlorinated, unsaturated metabolites. Chlorinated phenols may be formed and excreted as glucuronides. In a detailed discussion of the biodegradation of gamma-HCH, the reaction mechanisms involved were critically reviewed (Kurihara and Nakajima, 1980). Oxygenation or glutathione conjugation are important initial stages in metabolism. Key intermediates in the metabolic pathways are hexachlorocyclohexene (18), pentachlorocyclohexene (5) and tetrachlorocyclohexene (6) and these have been identified in a number of organisms (Macholz and Kujawa, 1985).
  • Solubility in water Wt % at 20 °C: 30.31 in acetone, 22.42 in benzene, 19.35 in chloroform, 17.22 in ether, 6.02 in ethanol (Windholz et al., 1983)
    9.76 and 13.97 g/L in hexane at 10 and 20 °C, respectively (shake flask-GC, Mills and Biggar, 1969)
    92.8 g/kg in triolein at 25 °C (Chiou and Manes, 1986)
  • 輸送方法 UN2761 Organochlorine pesticides, solid, toxic, Hazard Class: 6.1; Labels: 6.1-Poisonous materials.
  • 純化方法 Crystallise it from EtOH. Purify it also by zone melting. Possible CANCER AGENT, TOXIC. [: Beilstein 1 H 23, : Beilstein 5 I 8, many isomers : Beilstein 5 III 41, 5 IV 55.]
  • Degradation Gamma-HCH is extremely stable to light, air, temperatures up to 180 °C, and to acids. It undergoes dechlorination in alkalis with DT50 values (22 °C) of 191 days (pH 7) and 11 hours (pH 9). It is photodegraded in organic solvents (2-propanol or methanol) by UV irradiation (254 nm).
  • Toxicity evaluation The acute toxicity of lindane depends on the age, sex, and animal species, and on the route of administration. The oral LD50 in mice, rats, and guinea pigs is 86, 125–230, and 100–127 mg/kg, respectively. In contrast, most of the other isomers were considerably more toxic (94,95). Some of the other toxic responses caused by lindane in laboratory animals include hepato- and nephrotoxicity, reproductive and embryotoxicity, mutagenicity in some short-term in vitro bioassays, and carcinogenicity (80). The mechanism of the lindane-induced response is not known. Only minimal data are available on the mammalian toxicities of hexachlorocyclopentadiene.
  • 不和合性 Lindane decomposes on contact with powdered iron, aluminum, and zinc and with alkalis producing trichlorobenzene. Corrosive to metals
  • 廃棄物の処理 For the disposal of lindane, a process has been developed involving destructive pyrolysis @ 400-500℃ with a catalyst mixture which contains 5%-10% of either cupric chloride, ferric chloride; zinc chloride; or aluminum chloride on activated carbon. Consult with environmental regulatory agencies for guidance on acceptable disposal practices. Generators of waste containing this contaminant (≥100 kg/mo) must conform with EPA regulations governing storage, transportation, treatment, and waste disposal.
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  • 製品カタログ:47498
  • 優位度:58
  • 名前:career henan chemical co
  • 電話番号:13203830695 0086-371-86658258
  • ファックス番号:0086-371-86658258
  • 電子メール:factory@coreychem.com
  • 国籍:CHINA
  • 製品カタログ:29864
  • 優位度:58
  • 名前:Hefei TNJ Chemical Industry Co.,Ltd.
  • 電話番号:0551-65418671
  • ファックス番号:0551-65418697
  • 電子メール:sales@tnjchem.com
  • 国籍:CHINA
  • 製品カタログ:37441
  • 優位度:58
  • 名前:Dideu Industries Group Limited
  • 電話番号:029-88380327
  • ファックス番号:
  • 電子メール:Service@dideu.com
  • 国籍:CHINA
  • 製品カタログ:30013
  • 優位度:58
  • 名前:AFINE CHEMICALS LIMITED
  • 電話番号:008657185134551
  • ファックス番号:008657185134895
  • 電子メール:info@afinechem.com
  • 国籍:CHINA
  • 製品カタログ:15559
  • 優位度:58
  • 名前:Henan Alfa Chemical Co., Ltd
  • 電話番号:+8619139973225
  • ファックス番号:
  • 電子メール:adam@alfa-chemical.com;sales4@alfachem.cn
  • 国籍:China
  • 製品カタログ:12155
  • 優位度:58
  • 名前:Mainchem Co., Ltd.
  • 電話番号:+86-0592-6210733
  • ファックス番号:+86-0592-6210733
  • 電子メール:sale@mainchem.com
  • 国籍:CHINA
  • 製品カタログ:32439
  • 優位度:55
  • 名前:Chemwill Asia Co.,Ltd.
  • 電話番号:86-21-51086038
  • ファックス番号:86-21-51861608
  • 電子メール:chemwill_asia@126.com;sales@chemwill.com;chemwill@hotmail.com;chemwill@gmail.com
  • 国籍:CHINA
  • 製品カタログ:23975
  • 優位度:58
58-89-9, リンダン キーワード:
  • 58-89-9
  • JUCUTIN(R)
  • KEWLL(R)
  • ISOTOX(R)
  • LOREXANE(R)
  • 'LGC' (1103)
  • 'LGC' (1104)
  • LINTOX(R)
  • LINDANE
  • GAMMA-1,2,3,4,5,6-HEXACHLOROCYCLOHEXANE
  • G-BHC
  • GAMMA-HEXACHLOROCYCLOHEXANE
  • GAMMA-HCH
  • GAMMEXANE
  • D-BHC
  • D-HCH
  • DELTA-HEXACHLOROCYCLOHEXANE
  • DELTA-HCH
  • DELTA-BENZENEHEXACHLORIDE
  • DELTA-BHC
  • APHTIRIA
  • APARASIN(R)
  • BHC (DELTA ISOMER)
  • BHC GAMMA ISOMER
  • BENZENE HEXACHLORIDE
  • BENZENE HEXACHLORIDE (GAMMA-ISOMER)
  • BEN-HEX(R)
  • GAMMA-BHC, 1X1ML, MEOH, 20UG/ML
  • LINDAN PESTANAL (GAMMA-HEXACHLORO- CYCLO
  • LINDANE, 1GM, NEAT
  • Lindan solution
  • 1,2,3,4,5,6-ヘキサクロロシクロヘキサン (γ-異性体)
  • ゲキサン
  • ガンマ-BHC
  • リンダトクス
  • ベンゼンヘキサクロリド
  • ロレキサン
  • アグロシド
  • γ-リンダン
  • ガンマ-HCH
  • 1α,2α,3β,4α,5α,6β-ヘキサクロロシクロヘキサン
  • リンダン
  • クウェル
  • リンデン
  • ヘキサクロロシクロヘキサン
  • γ-ヘキサクロロシクロヘキサン
  • ヘキサクロラン
  • Γ-BHC標準品
  • Γ-HCH標準品
  • Γ-HCH標準液 CRM4203-A
  • γヘキサクロロシクロヘキサン
  • γ-ヘキサクロロシクロヘキサン (BHC)
  • γ-ヘキサクロロシクロヘキサン(BHC)
  • γ-ヘキサクロロシクロヘキサン(γ-HCH又はリンデン)
  • γ-ヘキサクロロシクロヘキサン、リンデン
  • ベンゼンヘキサクロリド (γ-異性体)
  • r-1,c-2,t-3,c-4,c-5,t-6-ヘキサクロロシクロヘキサン
  • 1,2,3,4,5,6-ヘキサクロロシクロヘキサン (リンデン)
  • Γ‐HCH標準品
  • Γ‐HCH標準液 CRM4203‐A
  • リンデンΓ-BHC
  • Γ-BHC BHCNDリンデンANDARD
  • リンデン STANDARD
  • Γ-HCH標準液
  • Γ-BHC (13C6, 100±10ΜG/ML ノナン溶液)
  • γ-BHC BHCndリンデンandard, 1000 µg/mL in MeOH
  • リンデン Standard, 100 µg/mL in MeOH
  • リンデン Standard, 1000 µg/mL in MeOH
  • リンデン Standard, 2.0 ng/µL in Isooctane
  • リンデン Standard, 200 ng/µL in Isooctane
  • 分析化学
  • 環境ホルモン
  • 塩素化化合物 (環境ホルモン)
  • 防疫用殺虫剤
  • 有機塩素系殺虫剤