다이에틸아민
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다이에틸아민 속성
- 녹는점
- -50 °C (lit.)
- 끓는 점
- 55 °C (lit.)
- 밀도
- 0.707 g/mL at 25 °C (lit.)
- 증기 밀도
- 2.5 (vs air)
- 증기압
- 14.14 psi ( 55 °C)
- 굴절률
- n
20/D 1.385(lit.)
- 인화점
- −20 °F
- 저장 조건
- Store below +30°C.
- 용해도
- H2O: 20°C에서 용해성 1M, 투명, 무색
- 산도 계수 (pKa)
- 11.02(at 40℃)
- 물리적 상태
- 액체
- 색상
- 무색의
- 냄새
- 암모니아성; 날카롭고 비린내 나는.
- 상대극성
- 0.145
- 수소이온지수(pH)
- 13 (100g/l, H2O, 20℃)
- pH 범위
- Strong alkaline
- Odor Threshold
- 0.048ppm
- ?? ??
- 암모니아의
- 폭발한계
- 2.0-11.8%(V)
- 수용성
- 녹는
- 감도
- Air Sensitive
- Merck
- 14,3111
- BRN
- 605268
- Henry's Law Constant
- 2.56(x 10-5 atm?m3/mol) at 25 °C (Christie and Crisp, 1967)
- 노출 한도
- NIOSH REL: TWA 10 ppm (30 mg/m3), STEL 25 ppm (75 mg/m3), IDLH 200 ppm; OSHA PEL: TWA 25 ppm; ACGIH TLV: TWA 5 ppm, STEL 15 ppm (adopted).
- Dielectric constant
- 3.7(20℃)
- 안정성
- 안정적인. 가연성이 높습니다. 강한 산화제와 호환되지 않습니다.
- InChIKey
- HPNMFZURTQLUMO-UHFFFAOYSA-N
- LogP
- 0.58 at 20℃
- CAS 데이터베이스
- 109-89-7(CAS DataBase Reference)
안전
- 위험 및 안전 성명
- 위험 및 사전주의 사항 (GHS)
위험품 표기 | F,C | ||
---|---|---|---|
위험 카페고리 넘버 | 11-20/21/22-35 | ||
안전지침서 | 16-26-29-36/37/39-45-3 | ||
유엔번호(UN No.) | UN 1154 3/PG 2 | ||
OEB | A | ||
OEL | TWA: 10 ppm (30 mg/m3), STEL: 25 ppm (75 mg/m3) | ||
WGK 독일 | 1 | ||
RTECS 번호 | HZ8750000 | ||
F 고인화성물질 | 10-23 | ||
자연 발화 온도 | 594 °F | ||
TSCA | Yes | ||
위험 등급 | 3 | ||
포장분류 | II | ||
HS 번호 | 29211990 | ||
유해 물질 데이터 | 109-89-7(Hazardous Substances Data) | ||
독성 | LD50 orally in rats: 540 mg/kg (Smyth) | ||
IDLA | 200 ppm | ||
기존화학 물질 | KE-13688 |
다이에틸아민 C화학적 특성, 용도, 생산
용도
1. 의약품 및 농약의 중간 및 고무 촉진제로 사용 2. 분석 시약 및 방부제뿐만 아니라 유기 합성 및 염료 제조에 사용됩니다. 3. 그것은 살충제 인 포스 파민, 피리 미딘 및 제초제의 중간체입니다. 4. 용제 및 화학 원료 중간체독성
이 제품은 매우 자극적이며 부식성이 있습니다. 이 제품의 증기 나 안개를 흡입하면 후두 부종, 기관지염, 화학적 폐렴, 폐부종이 발생할 수 있습니다. 고농도의 흡입은 사망을 유발할 수 있습니다. 증기는 눈에 자극적이며 각막 부종을 유발할 수 있습니다. 액체 나 안개가 눈에 자극을 주거나 화상을 입을 수 있습니다. 장시간 피부에 접촉하면 화상을 입을 수 있습니다. 구강은 소화관을 태운다. 만성 영향 : 반복 된 피부 접촉은 알레르기 성 피부염을 유발할 수 있습니다.개요
Diethylamine is a colourless, strongly alkaline, fish odour liquid, and highly inflammable. It has an ammonia-like odour and is completely soluble in water. On burning, diethylamine releases ammonia, carbon monoxide, carbon dioxide, and nitrogen oxides. Diethylamine is used in the production of pesticides. It is used in a mixture for the production of DEET which goes into the repellents that are found readily in supermarkets for general use.물리적 성질
Colorless liquid with a fishy, ammonia-like odor. Experimentally determined detection and recognition odor threshold concentrations were 60 μg/m3 (20 ppbv) and 180 μg/m3 (60 ppbv), respectively (Hellman and Small, 1974). Diethylamine is a very strong base in aqueous solution (pKb = 3.0). Its chemistry is governed by the unshared electron pair on the nitrogen, thus it tends to react with acids to form salts.출처
Diethylamine occurs in low concentrations in food and other biological materials. Concentrations (in p.p.m.) in fresh products include: spinach (15), apples (3), butterbeans (2.4), shelled peas (0.1), bean salad (1.5) and red cabbage (2.4) (HSDB 1989). Pickled vegetables contain 0-3.2 p.p.m. diethylamine while concentrations (in p.p.m.) in other materials include herring (0-5.2), barley (5.7), hops (3.1), boiled beef (2), tobacco leaf (0.1-35) and cigarette smoke concentrate (0-0.4). Interest in the occurrence of diethylamine in foods arises in part because of its possible formation of a carcinogenic N-nitroso derivative (Neurath et al 1977). Diethylamine has been reported in the exhaust from a gasoline engine (Hampton et al 1982).용도
Diethylamine is manufactured by heating ethyl chloride and alcoholic ammonia under pressure or by hydrogenation of aziridines in the presence of catalysts. DEA is used as a solvent, as a rubber accelerator, in the organic synthesis of resins, dyes, pesticides, and pharmaceuticals, in electroplating, and as a polymerization inhibitor. Other applications include uses as a corrosion inhibitor. It was reported noneffective as a skin depigmentator.생산 방법
Diethylamine is produced using the three methods also used for the manufacture of ethylamine with very slight modification.Diethylamine Synthesis
1. N,N-Diethyl-3-methylbenzamide + Ethylene Glycol + NaOH + Heat
2. Ethylchloride + Ammonia (forms diethylamine HCL)
3. Ethanol + Ammonia + Sulfuric Acid
The most widely used method is the passing of ammonia and ethanol over a catalyst such as alumina or silica (Schweizer et al 1978). Diethylamine can be separated from the mixture by selective distillations and extractions.
정의
ChEBI: Diethylamine is a secondary aliphatic amine where both N-substituents are ethyl. It is a conjugate base of a diethylammonium.일반 설명
A clear colorless liquid with an ammonia-like odor. Density 5.9 lb / gal. Flash point -15°F. A respiratory irritant. Corrosive to the eyes and skin. Vapors heavier than air. Toxic oxides of nitrogen produced during combustion.공기와 물의 반응
Highly flammable. Soluble in water. Sensitive to heat. May be sensitive to prolonged exposure to air.반응 프로필
It is incompatible with several chemical substances such as strong oxidisers, acids, cellulose nitrate, some metals, and dicyanofuroxan. N-nitrosamines, many of which are known to be potent carcinogens, may be formed when diethylamine comes in contact with nitrous acid, nitrates, or atmospheres with high nitrous oxide concentrations.건강위험
Diethylamine can be harmful if it is inhaled, swallowed, or in contact with skin. Vapors can irritate the eyes and cause irritation of the respiratory tract, leading to coughing and chest pain. Liquid diethylamine can cause severe burns to the eyes and skin. Vision became misty and halos appeared several hours after workmen were exposed to the vapors of amines such as diethylamine (Grant 1986). The edema of the corneal epithelium, which is principally responsible for the disturbances in vision, clears after one or more days, depending on the severity of exposure. Photophobia and discomfort from roughness of the corneal surface also can occur after greater exposure to the amine.화학 반응
Reactivity with Water No reaction; Reactivity with Common Materials: No hazardous reaction; Stability During Transport: Stable; Neutralizing Agents for Acids and Caustics: Flush with water; Polymerization: Not pertinent; Inhibitor of Polymerization: Not pertinent.공업 용도
Diethylamine, like many of the other short chain aliphatic amines, has achieved widespread industrial use as an intermediate in the manufacture of a number of commercial products. Among these are included insecticides, pharmaceuticals, textile finishing agents, and corrosion inhibitors (Hawley 1981; Schweizer et al 1978). It is used as a polymerization inhibitor and/or catalyst in the polymer industry and in the manufacture of surfactants and rubber processing accelerators. This amine also is useful as a depilatory agent for animal skins, as a selective solvent for the removal of impurities from oils, fats, and waxes, and as a flotation agent in the petroleum industry (NIOSH/OSHA 1981; HSDB 1989).Safety Profile
Moderately toxic by ingestion, inhalation, and skin contact. A skin and severe eye irritant. Exposure to strong vapor can cause severe cough and chest pains. Contact with liquid can damage eyes, possibly permanently; contact with skin causes necrosis and vesciculation. A very dangerous fire hazard when exposed to heat, flame, or oxidizers. To fight fire, use alcohol foam, CO2, dry chemical. Explodes on contact with dicyanofurazan. Violent reaction with sulfuric acid. Ignites on contact with cellulose nitrate of sufficiently high surface area. When heated to decomposition it emits toxic fumes of NOx. See also MINES.Toxicology
Exposure to low vapor concentrations are reported to transiently impair vision in humans (reduction of sensitivity to light): no-effect threshold 0.022 – 0.028 mL/m3 ( 0.08mg/m3 ). The odor threshold in air is ca. 0.02 – 0.3 mL/m3 ( 0.9 mg/m3 ). Transient physiological effects in rats after 90-d exposure to vapors were reported to already be visible at 0.37 – 4.19 mg/m3 with no effects at 0.05 mg/m3 , but with morphological, apparently reversible changes in the lung and cerebral neurons at the highest concentration. On the other hand, 50 mL/m3 (150 mg/m3 ) was the lowest concentration to show mild, but signifi- cant effects in the lung and liver of rabbits on prolonged inhalation. There were no visible signs of toxicity following exposure of rats to 25 mL/m3 (75 mg/m3 ) for 120 d, but a moderate, bronchiolar hyperplasia of lymphoid cells. It was assumed that diethylamine may exert a certain neurotoxic effect, which, however, was not confirmed by others.Carcinogenicity
No evidence of mutagenicity was seen in Ames bacterial assays.8 Diethylamine has an ammonia-like odor that is detectable at 0.13ppm.The 2003 ACGIH threshold limit valuetime- weighted average (TLV-TWA) for diethylamine is 5ppm (15mg/m3) with a short-term excursion limit of 15ppm (45mg/m3) and an A4-not classifiable as a human carcinogen designation; there is a notation for skin absorption.
환경귀착
Photolytic. Low et al. (1991) reported that the photooxidation of aqueous secondary amine solutions by UV light in the presence of titanium dioxide resulted in the formation of ammonium and nitrate ions.Chemical/Physical. Diethylamine reacted with NOx in the dark forming diethylnitrosamine. In an outdoor chamber, photooxidation by natural sunlight yielded the following products: diethylnitramine, diethylformamide, diethylacetamide, ethylacetamide, ozone, acetaldehyde, and peroxyacetyl nitrate (Pitts et al., 1978).
Reacts with mineral acids forming water-soluble salts (Morrison and Boyd, 1971).
신진 대사
Little information is available regarding the metabolism of diethylamine. The amine can be readily absorbed from the respiratory and gastrointestinal tract. It has been reported that following oral administration of diethylamine hydrochloride to humans, much of the amine was recovered in the urine (Beard and Noe 1978). This suggests that it is not readily metabolized and, therefore, may not be a substrate for monoamine oxidase. When administered intraperitoneally to rats, it was moderately inhibitory with respect to liver monoamine oxidase (Valiev 1974). Diethylamine may serve as a precursor for the formation of the reportedly carcinogenic N-nitrosoamines and, indeed, when a diethylamine containing liquid was examined for nitrosation reactions under simulated conditions of the human stomach, N-nitrosodiethylamine was formed (Ziebarth 1985).저장
Diethylamine should be protected from physical damage. It should be kept stored in a cool, dry, well-ventilated location, away from incompatible chemical substances and away from fi re hazard and smoking areas. The containers should be bonded and grounded for transfer to avoid static sparks. Storage and use areas should be no smoking areas.Purification Methods
Dry diethylamine with LiAlH4 or KOH pellets. Reflux with, and distil it from, BaO or KOH. Convert it to the p-toluenesulfonamide and crystallise to constant melting point from dry pet ether (b 90-120o), then hydrolyse with HCl, excess NaOH is added, and the amine is passed through a column of activated alumina. Redistil the amine and dry it with activated alumina before use [Swift J Am Chem Soc 64 115 1942]. [Beilstein 4 III 313.] § A polystyrene diethylaminomethyl supported version is commercially available.주의 사항
Occupational workers and users should be very careful during the use and chemical management of diethylamine. Workers should wear impervious protective clothing, including boots, gloves, a laboratory coat, apron or coveralls, as appropriate, to prevent skin contact. The chemical is very hazardous, corrosive, and harmful, and is a very flammable liquid and vapor. Exposures to vapor may cause fl ash fi re. It causes burns and adverse effects to the cardiovascular system. Workers should use chemical safety goggles and a full-face shield to avoid splashing of the chemical substance. An eye-wash fountain and quickdrench facilities in the work area should be maintained by the chemical management unit.다이에틸아민 준비 용품 및 원자재
원자재
준비 용품
디에틸시안아미드
테트라에틸티우람디설파이드
7-(DIETHYLAMINO)-5-METHYL-S-TRIAZOLO[1,5-A]PYRIMIDINE
2-(N,N-디에틸아미노카르보닐)페닐보론산
디에틸아미노아세토니트릴
ESFENVALERATE FREE ACID METABOLITE
아연 다이에틸다이싸이오카바메이트
5-아미노-3-메틸-티오펜-2,4-디카르복실산디메틸에스테르
FAST RED SALT ITR
2-AMINO-6-METHYL-4,5,6,7-TETRAHYDRO-1-BENZOTHIOPHENE-3-CARBONITRILE
1,4,6-Trimethyl-1H-pyrazolo[3,4-b]pyridin-3-ylamine ,97%
2-아미노-5,6-디하이드로-4H-사이클로펜타[B]티오펜-3-카보니트릴
2-아미노-4,5,6,7-테트라히드로-1-벤조티오펜-3-카보니트릴
2-AMINO-4,5-DIMETHYL-THIOPHENE-3-CARBONITRILE
살리실산벤질
4'-Iodoacetophenone
N,N-DIETHYLNICOTINAMIDE
리도카인 수화염화물
디에틸디티오카르밤산 디에틸암모늄 염
3-(디에틸아미노)프로판산
N,N-Diethyl-2-chloropropionamide
Etamsylate
2-히드록시-4,6-디메틸피리딘-3-카르보니트릴
(5-브로모-피리미딘-2-일)-디에틸-아민
프로카인 하이드로클로라이드
디에틸아민 하이드로클로라이드
4-페닐-1-(p-톨릴술포닐)피페리딘-4-카르복실산
Montelukast
BIS(DIETHYLAMINO)CHLOROPHOSPHINE
벤질 3-페닐프로펜산
2-Chloro-3-cyano-4,6-dimethylpyridine
1,1-diethylguanidine hydrochloride
디에틸카바모일클로라이드
패스트레드ITR
디트
다이에틸아미노트라이메틸렌아민
coating adhesive tiemao 102
DIETHYLCARBAMAZINE
TRIS(DIETHYLAMINO)PHOSPHINE
4,6-디메틸-1H-피라졸로[3,4-B]피리딘-3-아민
다이에틸아민 공급 업체
글로벌( 514)공급 업체
공급자 | 전화 | 이메일 | 국가 | 제품 수 | 이점 |
---|---|---|---|---|---|
Hebei Chuanghai Biotechnology Co,.LTD | +86-13131129325 |
sales1@chuanghaibio.com | China | 5893 | 58 |
Capot Chemical Co.,Ltd. | +86-(0)57185586718 +86-13336195806 |
sales@capot.com | China | 29791 | 60 |
Henan Tianfu Chemical Co.,Ltd. | +86-0371-55170693 +86-19937530512 |
info@tianfuchem.com | China | 21639 | 55 |
Shanghai Time Chemicals CO., Ltd. | +86-021-57951555 +8617317452075 |
jack.li@time-chemicals.com | China | 1803 | 55 |
Hefei TNJ Chemical Industry Co.,Ltd. | +86-0551-65418679 +8618949832763 |
info@tnjchem.com | China | 2986 | 55 |
Tianjin Zhongxin Chemtech Co., Ltd. | +86-022-66880623 +8618622897568 |
sales@tjzxchem.com | China | 563 | 58 |
Shanxi Naipu Import and Export Co.,Ltd | +86-13734021967 +8613734021967 |
kaia@neputrading.com | China | 1001 | 58 |
career henan chemical co | +86-0371-86658258 +8613203830695 |
sales@coreychem.com | China | 29886 | 58 |
SHANDONG ZHI SHANG CHEMICAL CO.LTD | +86 18953170293 |
sales@sdzschem.com | China | 2930 | 58 |
Hubei Jusheng Technology Co.,Ltd. | 18871490254 |
linda@hubeijusheng.com | CHINA | 28172 | 58 |