우레탄

우레탄
우레탄 구조식 이미지
카스 번호:
51-79-6
한글명:
우레탄
동의어(한글):
에틸카바메이트;우레탄;카바미드산에틸;에틸카바메이트;우레탄(에틸카바메이트);O-에틸우레탄;에틸 카바메이트;에틸우레탄;에틸카르밤산염;카르밤산,에틸에스테르
상품명:
Urethane
동의어(영문):
ETHYL CARBAMATE;Uretan;Urethan;Estane 5703;rethane;ethylurethan;ETHYLURETHANE;CARBAMIC ACID ETHYL ESTER;ETHYL CARBAMATE (URETHANE);x41
CBNumber:
CB4368670
분자식:
C3H7NO2
포뮬러 무게:
89.09
MOL 파일:
51-79-6.mol
MSDS 파일:
SDS

우레탄 속성

녹는점
48-50 °C(lit.)
끓는 점
182-184 °C(lit.)
밀도
1.10
증기 밀도
3.07 (vs air)
증기압
10 mm Hg ( 77.8 °C)
굴절률
1.4144
인화점
198 °F
저장 조건
Sealed in dry,Room Temperature
용해도
물에 약간 용해됨
물리적 상태
결정 또는 결정성 분말
산도 계수 (pKa)
13.58±0.50(Predicted)
색상
하얀색
수소이온지수(pH)
pH(50g/l, 25℃) : 5.0~7.0
수용성
약간 용해됨
Merck
14,9874
BRN
635810
Dielectric constant
14.2(50℃)
안정성
안정적인. 강산, 강염기, 강산화제와 호환되지 않습니다.
LogP
-0.150
CAS 데이터베이스
51-79-6(CAS DataBase Reference)
IARC
2A (Vol. 7, Sup 7, 96) 2010
NIST
Urethane(51-79-6)
EPA
Urethane (51-79-6)
안전
  • 위험 및 안전 성명
  • 위험 및 사전주의 사항 (GHS)
위험품 표기 T
위험 카페고리 넘버 45-22
안전지침서 53-45-99
유엔번호(UN No.) UN 3077 9 / PGIII
WGK 독일 3
RTECS 번호 FA8400000
TSCA Yes
HS 번호 29241990
유해 물질 데이터 51-79-6(Hazardous Substances Data)
독성 MLD i.p. in mice: 2.1-2.2 g/kg (Franklin)
기존화학 물질 2005-1-548
유해화학물질 필터링 2005-1-548
중점관리물질 필터링 별표1-4
함량 및 규제정보 물질구분: 유독물질; 혼합물(제품)함량정보: 에틸 카바메이트 및 이를 1% 이상 함유한 혼합물
그림문자(GHS): GHS hazard pictogramsGHS hazard pictograms
신호 어: Danger
유해·위험 문구:
암호 유해·위험 문구 위험 등급 범주 신호 어 그림 문자 P- 코드
H302 삼키면 유해함 급성 독성 물질 - 경구 구분 4 경고 GHS hazard pictograms P264, P270, P301+P312, P330, P501
H350 암을 일으킬 수 있음 (노출되어도 암을 일으키지 않는다는 결정적인 증거가 있는 노출경로가 있다면 노출경로 기재) 발암성 물질 구분 1A, 1B 위험 GHS hazard pictograms
예방조치문구:
P201 사용 전 취급 설명서를 확보하시오.
P308+P313 노출 또는 접촉이 우려되면 의학적인 조치· 조언를 구하시오.
NFPA 704
2
0

우레탄 MSDS


Carbamic acid ethyl ester

우레탄 C화학적 특성, 용도, 생산

개요

Ethyl carbamate occurs as colourless or white columnar crystals or granular powder. It is very soluble in water. With heat, ethyl carbamate undergoes decomposition and emits toxic fumes of carbon monoxide, carbon dioxide, and nitrogen oxides. Ethyl carbamate is used as an intermediate in the synthesis of a number of chemical products, for example, pharmaceuticals, in biochemical research and medicine, and as a solubiliser and co-solvent for pesticides and fumigants. Prior to World War II, ethyl carbamate saw relatively heavy use in the treatment of multiple myeloma before it was found to be toxic, carcinogenic, and largely ineffective. However, due to U.S. FDA regulations, ethyl carbamate has been withdrawn from pharmaceutical use. However, small quantities of ethyl carbamate are also used in laboratories as an anaesthetic for animals.

화학적 성질

Urethane is a colorless, almost odorless crystalline solid or powder.

출처

Urethane (ethyl carbamate) occurs as a natural byproduct in fermented products such as wine, liquors, yogurt, beer, bread, olives, cheeses, and soy sauces. Whereas urethane has a known cancer etiology in experimental animals, no such relationship has yet been proven in humans. Alcohol may act by blocking the metabolism of urethane, and thus exert a protective effect in humans consuming alcoholic beverages.

용도

The primary use of urethane has been as a chemical intermediate in preparation of amino resins (IARC 1974). The process involves a reaction with formaldehyde to give hydroxymethyl derivatives that are used as cross-linking agents in permanent-press textile treatments designed to impart wash-and-wear properties to fabrics. Urethane isalso used as a solubilizer and co-solvent in the manufacture of pesticides, fumigants, and cosmetics, as an intermediate in the manufacture of pharmaceuticals, and in biochemical research (HSDB 2009). Urethane was formerly used as an active ingredient in drugs prescribed for the treatment of neoplastic diseases, as a sclerosing solution for varicose veins, as a hypnotic, and as a topical bactericide. It is also used in veterinary medicine as an anesthetic (IARC 1974). Urethane is produced naturally during many fermentation processes(Zimmerli and Schlatter 1991).

정의

A poisonous flammable organic compound, used in medicine, as a solvent, and as an intermediate in the manufacture of polyurethane resins.

World Health Organization (WHO)

Urethane was formerly used as an antineoplastic agent in the treatment of chronic myeloid leukaemia. It is also a mild hypnotic which has been used as an anaesthetic for veterinary practice. It has been reported to have both a carcinogenic and mutagenic potential. Although urethane continues to be used as an industrial solvent, WHO has no information to suggest that it remains commercially available in pharmaceutical preparations.

일반 설명

Odorless colorless crystals or white powder. Sublimes readily at 217°F and 54 mm Hg. Cooling saline taste.

공기와 물의 반응

Water soluble. Aqueous solutions are neutral to litmus .

반응 프로필

Urethane is incompatible with alkalis, acids, chloral hydrate, camphor, menthol and thymol. Also incompatible with antipyrine and salol. May react with strong oxidizing agents. Liquefies with benzoic acid, resorcinol and salicylic acid. Reacts with phosphorus pentachloride to form an explosive product .

위험도

Toxic by ingestion.

Safety Profile

Confirmed carcinogen with experimental carcinogenic, neoplastigenic, and tumorigenic data. A transplacental carcinogen. Moderately toxic by ingestion, intraperitoneal, subcutaneous, intramuscular, parenteral, and intravenous routes. An experimental teratogen. Experimental reproductive effects. Human mutation data reported. Causes depression of bone marrow and occasionally focal degeneration in the brain. Can also produce central nervous system depression, nausea and vomiting. Has been found in over 1000 beverages sold in the United States. The most heavily contaminated liquors are bourbons, sherries, and fruit brandies (some had 1000 to 12,000 ppb urethane). Many whiskeys, table and dessert wines, brandies, and liqueurs contain potentially hazardous amounts of urethane. The allowable limit for urethane in alcoholic beverages is 125 ppb. It is formed as a side product during processing.Hot aqueous acids or alkalies decompose urethane to ethanol, carbon dioxide, and ammonia. Reacts with phosphorus pentachloride to form an explosive product. When heated it emits toxic fumes of NOx. Used as an intermedate in the manufacture of pharmaceuticals, pesticides, and fungicides. See also CARBAMATES.

잠재적 노출

Urethane is used as a chemical intermediate in manufacture of pharmaceuticals; pesticides, and fungicides; in the preparation of amino resins. It may be reacted with formaldehyde to give cross-linking agents which impart wash-and-wear properties to fabrics. It has also been used as a solubilizer and cosolvent in the manufacture of pesticides, fumigants, and cosmetics. It was formerly used in the treatment of leukemia. It occurs when diethylpyrocarbonate, a preservative used in wines, fruit juices, and soft drinks, is added to aqueous solutions.

Carcinogenicity

Urethane is reasonably anticipated to be a human carcinogen based on sufficient evidence of carcinogenicity from studies in experimental animals.

환경귀착

Urethane may be released to the environment in various waste streams. If released to the atmosphere, urethane is expected to exist solely as a vapor in the ambient atmosphere. Vapor-phase urethane is degraded in the atmosphere by reaction with photochemically produced hydroxyl radicals with an estimated half-life of 2.2 days. If released to soil, urethane has very high mobility. Volatilization from moist soil surfaces does not occur. Biodegradation of urethane in soil may be important. If released into water, urethane is not adsorbed to suspended solids and sediment in the water column. Volatilization from water surfaces does not occur. The potential for bioconcentration in aquatic organisms is low based on an estimated bioconcentration factor (BCF) of 0.45. Urethane is resistant to hydrolysis under environmental conditions; hydrolysis half-lives of 3300 and 330 years at pH 7 and 8, respectively, were estimated for urethane. Urethane was judged easy to biodegrade in river die-away tests. Other biodegradation studies using activated sludge indicate urethane may biodegrade slowly.

Purification Methods

Urethane is best purified by fractional distillation, but it can be 20 25 1.4144. sublimed at ~103o/~50mm. It has also been recrystallised from *benzene. Its solubilitiy at room temperature is 2g/mL in H2O, 1.25g/mL in EtOH, 1.1g/mL in CHCl3, 0.67g/mL in Et2O and 0.03g/mL in olive oil. It is a suspected human carcinogen.[Beilstein 3 H 22, 3 IV 40.]

비 호환성

Dust may form explosive mixture with air. Incompatible with oxidizers (chlorates, nitrates, peroxides, permanganates, perchlorates, chlorine, bromine, fluorine, etc.); contact may cause fires or explosions. Keep away from alkaline materials, strong bases, strong acids, oxoacids, epoxides, gallium, perchlorate.

폐기물 처리

Consult with environmental regulatory agencies for guidance on acceptable disposal practices. Generators of waste containing this contaminant (≥100 kg/mo) must conform to EPA regulations governing storage, transportation, treatment, and waste disposal. Controlled incineration (incinerator equipped with a scrubber or thermal unit to reduce nitrogen oxides emissions).

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