75-08-1 - Names and IdentifiersNameEthanethiolSynonymsEM(TM) RTEthanethiolETHANETHIOLMERCAPTAN
E-posta adresi: info@standard-groups.com
| Adı | Ethanethiol |
| Eşanlamlar | EM(TM) RT Ethanethiol ETHANETHIOL MERCAPTAN C2 Mercaptan C2 Ethylmercaptan Ethyl mercaptan ETHYL MERCAPTAN 1-Mercaptoethane mercury diethanethiolate |
| CAS'ın | 75-08-1 |
| EINECS'in | 200-837-3 |
| InChI'nin | InChI=1/2C2H6S.Hg/c2*1-2-3;/h2*3H,2H2,1H3;/q;;+2/p-2 |
| Moleküler Formül | C2H6S |
| Molar Kütlesi | 62.13 |
| Yoğunluk | 0.839g/mLat 25°C(lit.) |
| Erime noktası | -148 °C |
| Boling Point | 35°C(lit.) |
| Flash Point | 1 ° F |
| JECFA Numarası | 1659 |
| Su Solubility | Soluble in alcohol, ether, waterMiscible with alcohol, petroleum naphtha, acetone, dilute alkali and ether. Slightly miscible with water. |
| Çözünürlük | 6.8g/l |
| Buhar Basıncı | 8.51 psi ( 20 °C) |
| Vapor Densitesi | 2.1 (vs air) |
| Görüntü | Liquid |
| Renk | Colorless |
| Odor | Strong chunk; offensive garlic. |
| Maruz kalma sınırı | TLV-TWA 0.5 ppm (～1.3 mg/m3 ) (ACGIHand MSHA); ceiling 10 ppm (OSHA); IDLH2500 ppm (NIOSH). |
| Merck'ın | 14,3726 |
| BRN | 773638 |
| pKa | 10.6(at 25℃) |
| Depolama Koşulları | +30 ° C'nin altında saklayın. |
| Kararlılık | Stable. Extremely flammable - note low flash point. Incompatible with oxidizing agents, strong acids. May form explosive mixtures with air. |
| Patlayıcı Sınır | 2.8-18%(V) |
| Kırılma Endeksi | n20/D 1.4306(lit.) |
| Fiziksel ve Kimyasal Özellikler | Colorless transparent oily liquid with strong persistent pungent garlic odor. Volatile in the air. melting point -147.89 ℃ boiling point 35 ℃ relative density 0.8391 refractive index 1.4310 soluble in water, 20 ° C in water solubility of 1.5% (weight ratio), soluble in alkaline water and ethanol, ether and other organic solvents. |
| Kullanım | For pesticide intermediates, warning gas |
| Risk Kodları | R11 - Çok ateşlenebilirPlease take the official translations! You find them here: http: // europa. eu. int/ eur- lex/ lex/ LexUriServ/ LexUriServ. do? uri=CELEX: 32001L0059: EN: HTML R20 - Inhalasyon yoluyla zararlı R50/53 - Su organizmaları için çok zehirli, su çevresinde uzun süredir negatif etkiler olabilir. Çek! R51/53 Su organizmaları için toksik, su ortamında uzun vadeli olumsuz etkilere neden olabilir. R12 - Extremely Flammable R20/22 - Nefes almak ve yutmak zorunda. |
| Güvenlik Açıklaması | S16 - Ateşme kaynaklarından uzak tutun. S25 - Avoid contact with eyes. S60 - Bu materyal ve konteynatı tehlikeli kaybı olarak silmeli. S61 - Çevre serbest bırakmayı engelleyin.Please take the official translations! You find them here: http: // europa. eu. int/ eur- lex/ lex/ LexUriServ/ LexUriServ. do? uri=CELEX: 32001L0059: EN: HTML Özel talimatlara / güvenlik veri çarşaflara bakın. Çek! |
| BM Kimlikleri | UN 2363 3/PG 1 |
| WGK Almanya | 3 |
| RTECS | KI9625000 |
| FLUKA MARKA F KODLARI | 13 |
| TSCA'nın | Evet. |
| HS Kodu | 2930 90 98 |
| Tehlike Sınıfı | 3 |
| Paketleme Grubu | I |
| Toksiklik | LD50 orally in Rabbit: 682 mg/kg |
| Aşağıdaki ürünler | Ethyl thioacetate |
| FEMA | 4258 | ETHANETHIOL |
| olfactory Threshold | 0.0000087ppm |
| Henry's Law Constant | 3.57(x 10-3 atm?m3/mol) at 25 °C (Przyjazny et al., 1983) |
| Uygulama | used in pesticide intermediates, warning gas ethanethiol is an important pesticide intermediate, for the synthesis of organophosphorus insecticides phorate phosphorus, phosphorus, isopropyl phosphorus, phosphorus absorption, methyl phosphorus absorption and herbicides, in addition, can also be used as reagents and gas odorants, liquid fuel additives, and for pharmaceutical synthesis. ethanethiol is an important pesticide intermediate, which is used in the production of organophosphorus pesticide isopropylphosphorus, phorate phosphorus, phorate phosphorus, internal phosphorus uptake, methyl phosphorus uptake, etc. It may also be used for the production of an antimicrobial agent 401. When the concentration of ethyl mercaptan in the air is only 50 billion times, the odor can be detected, so it can be used as a warning agent for natural gas and petroleum gas, reagent plus odor (the odor in the concentration of 0.00019mg/L can smell). Ethanethiol can also be used in pharmaceutical and other organic synthesis. useful as a stabilizer for adhesives and as an intermediate for chemical synthesis. |
| üretim yöntemi | 1. From the reaction of sodium ethyl sulfate and sodium hydrosulfide. The sodium ethyl sulfate used in this method was prepared from anhydrous ethanol and fuming sulfuric acid. The overall yield was 60%-65% (absolute ethanol). Domestic this method is more mature, the disadvantage is long route, low yield, high demand for raw materials. It is derived from the reaction of ethyl chloride with sodium hydrosulfide. The yield was more than 80% (based on chloroethanol). 3. From ethanol (or ethylene) and hydrogen sulfide by gas phase catalytic reaction. The reaction is carried out at atmospheric pressure, and the catalyst is impregnated with tungstic acid or sodium tungstate using activated alumina as a carrier. The reaction temperature was 360-380 °c. Ethanethiol yield (based on ethanol), up to 70%-79%. 4. Laboratory preparations can be made from thiourea and bromoethane. The preparation method includes an anhydrous ethanol method, a chloroethane method, an ethanol (ethylene) method, and the like. (1) anhydrous ethanol method with anhydrous ethanol, fuming sulfuric acid and sodium hydrosulfide as raw material. C2H5OH + H2SO4 · SO3 → C2H5OSO2OH + H2SO42C2H5OSO2OH + Na2CO3 → 2c2h2oso2ona + H2O + CO2 ↑ c2oso2ona + NaSH → C2H5SH + Na2SO4 this method is a mature production process in China, but it has a long route, the yield is low, the requirement for raw materials is high, the dosage of acid and alkali is large, and the equipment is corrosive. (2) the ethyl chloride method is obtained by reacting ethyl chloride with sodium hydrosulfide. C2H5Cl + NaSH → C2H5SH + NaCl this method has the advantages of simple process and high yield, Disadvantages are the need for pressure, high requirements for equipment, intermittent operation, high labor intensity, and limited sources of ethyl chloride. (3) the ethanol (or ethylene) method is obtained by reacting hydrogen sulfide gas with ethanol vapor or ethylene in the presence of a catalyst. C2H5OH + H2S → C2H5SH + H2O This method has the advantages of simple process, easy availability of raw materials, low cost, high product purity and continuous production. The main disadvantage is that the reaction temperature is high, hydrogen sulfide is highly toxic, and has strong corrosion to the equipment. |
| Kategori | flammable liquid |
| zehirli sınıf | zehirlenmek |
| Akut toksisite | oral-rat LD50: 682 mg/kg; Inhalation-mouse LC50: 2770 PPM/ 4 h |
| stimülasyon verileri | Skin-rabbits 500 mg/24 h mild; eye-rabbit 100 mg/24 h moderate |
| explosive hazard characteristics | explosive when mixed with air |
| yanılabilirlik tehlike özellikleri | in case of fire, high temperature, flammable water, oxidant; toxic sulfur dioxide gas |
| depolama ve taşıma özellikleri | The warehouse is ventilated and dried at low temperature; Stored separately from oxidants and acids |
| söndürme ajanı | dry powder, dry sand, dry stone powder, carbon dioxide, foam |
| Occupational Standard | TWA 1 mg/m3; Tel 1 mg/m3 |
| spontan yanma sıcaklığı | 570 ° F. |
| immediate life-and health-threatening concentration | 500 ppm |
Sorumluluktan vazgeçme: Yukarıdaki içerik yalnızca endüstri içindeki kişiler arasında referans ve iletişim amacıdır ve doğruluğunu veya eksiksizliğini garanti etmez. İlgili yasa ve düzenlemelere ve bu web sitesinin düzenlemelerine göre, ilgili ürünleri satın alan birimler veya bireyler geçerli nitelikler ve nitelik koşulları almalıdır.
Şirket Telefonu
+86-21-6420 0566
Çalışma saatleri
Pazartesi - Cuma
Cep telefonu:
13816217984
E-posta adresi:
info@qinsun-lab.com
