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1-부텐 구조식 이미지
카스 번호:
포뮬러 무게:
MOL 파일:

1-부텐 속성

−185 °C(lit.)
끓는 점
−6.3 °C(lit.)
증기 밀도
1.93 (vs air)
1939 mm Hg ( 21.1 °C)
Soluble in alcohol, benzene, and ether (Weast, 1986)
산도 계수 (pKa)
>14 (Schwarzenbach et al., 1993)
물리적 상태
Boiling Point
-6.47 °C
0.577 g/cm3(Temp: 25 °C)
Melting Point
-185 °C
Boiling Point
-6.47 °C
0.577 g/cm3(Temp: 25 °C)
Melting Point
-185 °C
222 mg/kg at 25 °C (shake flask-GC, McAuliffe, 1966)
Henry's Law Constant
(atm?m3/mol): 0.25 at 25 °C (Hine and Mookerjee, 1975)
CAS 데이터베이스
106-98-9(CAS DataBase Reference)
  • 위험 및 안전 성명
  • 위험 및 사전주의 사항 (GHS)
위험품 표기 F+,F
위험 카페고리 넘버 12
안전지침서 9-16-33
유엔번호(UN No.) UN 1012 2.1
WGK 독일 -
F 고인화성물질 4.5-31
자연 발화 온도 723 °F
위험 참고 사항 Extremely Flammable
위험 등급 2.1
포장분류 II
신호 어: Danger
유해·위험 문구:
암호 유해·위험 문구 위험 등급 범주 신호 어 그림 문자 P- 코드
H220 극인화성 가스 인화성 가스 구분 1 위험 P210, P377, P381, P403
H280 고압가스; 가열시 폭발할 수 있음 고압가스 압축가스
용존 가스
경고 P410+P403
P210 열·스파크·화염·고열로부터 멀리하시오 - 금연 하시오.
P377 누출성 가스 화재 시 : 누출을 안전하게 막을 수 없다면, 불을 끄려하지 마시오.
P381 누출의 경우, 모든 점화원을 제거하시오.
P410+P403 직사광선을 피하고 환기가 잘 되는 곳에 보관하시오.

1-부텐 C화학적 특성, 용도, 생산


CMC-Na는 선상 고분자 이온 성 셀룰로오스 에테르이며 나트륨 카르복시 메틸 셀룰로오스의 알칼리 화, 에테르 화, 중화, 세척 다른 프로세스들은 반응을 일으켰다. CMC는 일반적으로 CMC라고 불리는 수용성 소금입니다. CMC는 독창적 인 점착성, 수분 흡수 및 수분 보유 성질을 가지고 있습니다. 또한, CMC는 천천히 생분해 성을 갖는 천연 유래 셀룰로오스이기 때문에 친환경적으로 만든 후 소각 처리가 가능합니다.

유제 분산제

유화제는 에멀젼에서의 상간의 표면 장력을 향상시켜 균일하고 안정한 분산 시스템 또는 에멀젼을 형성하는 물질입니다. 유화제는 분자 내에 친수성기와 친수성기를 가진 표면 활성 물질입니다. 그들은 계면 장력을 감소시키고 에멀젼을 형성하는데 필요한 에너지를 감소시켜 유제의 에너지를 증가시키는 오일 / 물 계면에 집중합니다. 음이온 계면 활성제로서, 도데 실 벤젠 술폰산 나트륨은 표면 활성이 우수하고 친수성이다. 따라서, 도데 실 벤젠 술폰산 나트륨은 화장품, 식품, 인쇄 및 염색 에이즈 및 살충제와 같은 에멀젼의 제조에 널리 사용되어왔다.


1-Butene is a colourless, stable but polymerises exothermically, extremely flammable liquefied gas with an aromatic odour. It is insoluble in water and is one of the isomers of butane. 1-Butene readily forms explosive mixtures with air. It is incompatible with strong oxidising agents, halogens, halogen acids, metal salts, boron trifluoride, fluorine, and nitrogen oxides. 1-Butene of high purity is made by cracking naphtha and separating it from other products by an extra-high-purity distillation column. It is an important organic compound in the production of several industrial materials – for instance, linear low-density polyethylene (LLDPE), a more flexible and resilient polyethylene, and a range of polypropylene resins – and in the production of polybutene, butylene oxide, and the C4 solvents secondary butyl alcohol (SBA) and MEK. The vapour of 1-butene is heavier than air and may travel long distances to an ignition source and flash back.

화학적 성질

1-Butene is a colorless, extremely flammable liquefi ed gas with an aromatic odor. It is insol uble in water and is an isomer of butane. It is highly flammable and readily forms explo sive mixtures with air. 1-Butene of high purity is made by cracking naphtha and separating it from other products by an extra-high purity distillation column. However, 1-butene is incompatible with metal salts, fl uorine, nitrogen oxides, boron trifl uoride, halogen acids, halogens, and strong oxidizing agents. It is an important organic compound in the produc tion of several industrial materials, i.e., linear low density polyethylene (LLDPE), a more fl exible and resilient polyethylene, a range of polypropylene resins, and in the production of polybutene, butylene oxide and in the C4 solvents, secondary butyl alcohol (SBA) and methyl ethyl ketone (MEK). The vapor of 1-butene is heavier than air and may travel long distances to an ignition source and fl ash back.

물리적 성질

Butenes or butylenes are hydrocarbon alkenes that exist as four different isomers. Each isomer is a flammable gas at normal room temperature and one atmosphere pressure, but their boiling points indicate that butenes can be condensed at low ambient temperatures and/or increase pressure similar to propane and butane. The “2” designation in the names indicates the position of the double bond. The cis and trans labels indicate geometric isomerism. Geometric isomers are molecules that have similar atoms and bonds but different spatial arrangement of atoms. The structures indicate that three of the butenes are normal butenes, n-butenes, but that methylpropene is branched. Methylpropene is also called isobutene or isobutylene. Isobutenes are more reactive than n-butenes, and reaction mechanisms involving isobutenes differ from those of normal butenes.


Butenes are used extensively in gasoline production to produce high-octane gasoline compounds.Another large use of normal butenes in the petrochemical industry is in the production of 1,3-butadiene. Butene is used in the plastics industry to make both homopolymers and copolymers. Another use of 1-butene is in the production of solvents containing four carbons such as secondary butyl alcohol and methyl ethyl ketone (MEK).

생산 방법

Most butenes are produced in the cracking process in refineries along with other C-4 fractions such as the butanes. Butenes are separated from other compounds and each other by several methods. Isobutene is separated from normal butanes by absorption in a sulfuric acid solution. Normal butenes can be separated from butanes by fractionation. The close boiling points of butanes and butenes make straight fractional distillation an inadequate separation method, but extractive distillation can be used. Butenes can also be prepared from the dehydrogenation (elimination of hydrogen) of butane.


ChEBI: A butene with unsaturation at position 1.

일반 설명

Colorless gas.

공기와 물의 반응

Highly flammable. Insoluble in water.

반응 프로필

The unsaturated aliphatic hydrocarbons, such as 1-BUTENE, are generally much more reactive than the alkanes. Strong oxidizers may react vigorously with them. Reducing agents can react exothermically to release gaseous hydrogen. In the presence of various catalysts (such as acids) or initiators, compounds in this class can undergo very exothermic addition polymerization reactions. May react with oxidizing materials. Aluminum borohydride reacts with alkenes and in the presence of oxygen, combustion is initiated even in the absence of moisture.


Exposures to 1-butene cause the effects of an asphyxiant and/or an anesthetic (at high concentrations). Workers exposed to 1-butene develop eye irritation.


1-BUTENE is flammable. Vapor is heavier than air and may travel long distances to an ignition source and flash back.


In exhaust of gasoline-powered engines (1.8 vol % of total exhaust hydrocarbons) (quoted, Verschueren, 1983). Detected in California Phase II reformulated gasoline at a concentration of 170 mg/kg (Schauer et al., 2002).
Schauer et al. (2001) measured organic compound emission rates for volatile organic compounds, gas-phase semi-volatile organic compounds, and particle-phase organic compounds from the residential (fireplace) combustion of pine, oak, and eucalyptus. The gas-phase emission rate of 1-butene was 90.7 mg/kg of pine burned. Emission rates of 1-butene were not measured during the combustion of oak and eucalyptus.
Reported as an impurity (0.1 wt %) in 99.4 wt % trans-2-butene (Chevron Phillips, 2004).


Biological. Biooxidation of 1-butene may occur yielding 3-buten-1-ol, which may oxidize to give 3-butenoic acid (Dugan, 1972). Washed cell suspensions of bacteria belonging to the genera Mycobacterium, Nocardia, Xanthobacter, and Pseudomonas and growing on selected alkenes metabolized 1-butene to 1,2-epoxybutane (Van Ginkel et al., 1987).
Photolytic. Products identified from the photoirradiation of 1-butene with nitrogen dioxide in air are epoxybutane, 2-butanone, propanal, ethanol, ethyl nitrate, carbon monoxide, carbon dioxide, methanol, and nitric acid (Takeuchi et al., 1983).
The following rate constants were reported for the reaction of 1-butene and OH radicals in the atmosphere: 1.0 x 10-17 cm3/molecule?sec (Bufalini and Altshuller, 1965); 2.70 x 10-11 cm3/molecule?sec (Atkinson et al., 1979); 3.14 x 10-11 cm3/molecule?sec (Atkinson, 1990; Sablji? and Güsten, 1990). Reported photooxidation reaction rate constants for the reaction of 1-butene and ozone are 1.23 x 10-17, 1.0 x 10-17, 1.03 x 10-17 cm3/molecule?sec (Adeniji et al., 1981). Based on the reaction of 1-butene and OH radicals gas phase, the atmospheric lifetime was estimated to be 5.5 h in summer sunlight.
Chemical/Physical. Complete combustion in air yields carbon dioxide and water. Incomplete combustion will generate carbon monoxide.
Hydrolysis in water is not expected to be signicant because 1-butene is very volatile.

주의 사항

When working with 1-butene, occupational workers should wear proper protectives, preferably a NIOSH-approved full-face positive pressure supplied-air respirator or a self contained breathing apparatus (SCBA). Workers should not wear contact lenses.

1-부텐 준비 용품 및 원자재


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