스티렌 모노머

Styrene

HCID 7501CAS 100-42-5

기본 정보

표준 SMILES
C=Cc1ccccc1
InChIKey
PPBRXRYQALVLMV-UHFFFAOYSA-N
분자식
C8H8
평균 분자량
104.15 g/mol
단동위원소 질량
104.06260026

이름 및 식별자

우선 이름
Styrene
IUPAC
styrene
현지명
스티렌 모노머
영어명
Styrene
분자식
C8H8
분자량
104.15

이름 및 동의어

STYRENE100-42-5EthenylbenzenePhenylethyleneVinylbenzeneStyrolBenzene, ethenyl-CinnameneStyrene monomerPhenyletheneStyrolenePhenethylene
이름 더 보기
스티렌비닐벤젠스티렌모노머,억제제에텐일벤젠페닐에텐스타이렌스티렌모노머페닐에틸렌SMOligosaccharidemethyl 2-methylprop-2-enoate
VinylbenzolStyroleVinyl benzeneStyropol SOCinnamolStyrenBenzene, vinyl-Cinnamenol

데이터베이스 식별자

CAS
100-42-5、79637-11-9、98444-30-5
PubChem CID
7501
DTXSID
DTXSID2021284
ChEMBL
CHEMBL285235
ChEBI
CHEBI:27452
UNII
44LJ2U959V
EC Number
202-851-5、616-714-6、619-344-3
Nikkaji
J4.006A

물성

구조 계산 물성

XLogP
2.9
극성 표면적
0 Ų
수소 결합 공여자 수
0
수소 결합 수용자 수
0
회전 가능 결합 수
1
무거운 원자 수
8

물리화학적 성질

녹는점
-31 °C · -31 °C (lit.)
끓는 점
145 · 145-146 °C (lit.)
밀도
0.906 g/mL · 0.906 g/mL at 25 °C
증기 밀도
3.6 · 3.6 (vs air)
증기압
12.4 mm · 12.4 mm Hg ( 37.7 °C)
굴절률
20 · n20/D 1.546(lit.)
화학적 성질 · 1건

Styrene is a colorless or yellow, sweet odor liquid with a penetrating odor. It is produced during alkylation of benzene with ethylene. It is highly reactive and polymerizes rapidly with a violent explosive reaction. This demands proper handling, transportation, and storage by adding polymerization inhibitors in adequate quantities during these operations. Styrene monomer has been extensively used in the manufacture of chemical intermediates, fi lling components, plastics, resins, and stabilizing agents.

안전 및 규제

안전 데이터

OEB
A
OEL
TWA: 50 ppm (215 mg/m3), STEL: 100 ppm (425 mg/m3)
wgk
2
IDLA
700 ppm
tsca
TSCA listed
rtecs
WL3675000

화학 및 산업

응용 분야 · 7건

개요화학명은 비닐벤젠으로 일명 스티롤이라고도 한다. 무색의 액체이며 비중은 0.9로 물보다 낮고 비등점은 섭씨 1백45.1도, 인화점은 섭씨 32도이다. 유화제품을 크게 지방족탄화수소와 방향족탄화수소로 나누면 후자에 속하며 방향족의 벤젠계, 톨루엔계 크실렌계, 중벤젠계에 속하는 중간원료다.

용도폴리스틸렌, ABS, SBR 제조용으로 사용

개요Styrene has a characteristic, sweet, balsamic, almost floral odor that is extremely penetrating. Styrene occurs naturally in plants. It was first isolated from a resin called storax obtained from the inner bark of the Oriental sweet gum tree (Liquidambar orientalis) by Bonastre. In 1839, the German apothecary Eduard Simon prepared styrene by distilling it from storax and called it styrol. Simon observed it solidifi ed into a rubbery substance after being stored and believed it had oxidized into styrol oxide. Subsequent analysis showed the solid did not contain oxygen and it was renamed metastyrol. This was the first written record of polymerization in chemistry. In 1845, the English chemist, John Blyth, and the German chemist, August Wilhelm von Hofmann (1818 1892), observed that styrene was converted to polystyrene by sunlight and that styrene could be polymerized to polystyrene by heating in the absence of oxygen. It took another 70 years for the polymerization of styrene to be described by Hermann Staudinger (1881 1965) in the 1920s. This laid the foundation for the commercial polystyrene industry that developed in the 1930s.

용도메트포르민은 다낭성 난소 증후군치료에도 사용되며 다른 적응증도 연구중이다. 메트포르민은 간에서 포도당의 생성을 억제한다.

출처Reported found in cranberry and bilberry, currants, grape, parsley, milk and dairy products, whiskey, cocoa, coffee, tea, roasted filberts and roasted peanuts. Also reported found in fresh apple, guava fruit, pineapple, vinegar, butter, fish oil, black tea, roasted filbert, roasted peanut, soybean, plum brandy, apple brandy, Brazil nut, rice bran, Bourbon vanilla, grapes, peach, strawberry, onion, peas, bell pepper, cassia leaf, cheeses, parsley, milk, boiled and scrambled egg, lean fish, fish oil, cooked chicken and beef, rum, malt and Scotch whiskey, cider, grape, wine, cocoa, coffee, honey, cloudberry, plum, rose apple, beans, trassi, walnut, buckwheat, soursop, watercress, kiwifruit, wild rice, sapodilla fruit, nectarine, okra, crab, crayfish and pawpaw.

용도Styrene (monomer) is a viscous, highly flammable liquid that evaporates easily and polymerizes readily to polystyrene unless a stabilizer is added. Styrene is used in multiple industries, especially in reinforced plastics (e.g., fiberglass boats), and is widely used to make plastics and rubber, packaging materials (e.g., packing peanuts ), insulation for buildings, plastic pipes, food containers (e.g., takeout containers), and carpet backing) (ATSDR, 2010).

일반 설명A clear colorless to dark liquid with an aromatic odor. Flash point 90°F. Density 7.6 lb/gal. Vapors heavier than air and irritating to the eyes and mucous membranes. Subject to polymerization. If the polymerization takes place inside a closed container, the container may rupture violently. Less dense than water and insoluble in water. Used to make plastics, paints, and synthetic rubber.

제조 방법 · 2건

생산 방법Styrene is made by dehydrogenation of ethylbenzene at high temperature using metal catalysts: C6H5CH2CH2(g)→ C6H5CH = CH2(g) + H2(g). This is called the EB/SM (ethylbenzene/styrene monomer) process. Styrene can also be made by PO/SM (propylene oxide/styrene monomer) process). This process starts by oxidizing ethylbenzene (C6H5CH2CH2) to its hydroperoxide (C6H5CH(OOH)CH3), which is then used to oxidize propylene (CH3CH = CH2) to produce propylene oxide (CH3CH2CHO) and phenylethanol (C6H5CH(OH)CH3). The phenylethanol is then dehydrated to give styrene and water. Styrene can also be synthesized by reacting benzene and ethylene or natural gas.

Prepared from ethylbenzene or from phenylethanol.

공급사2 곳

斯百全化学(上海)有限公司021-021-021-67601398-809-809-809 15221380277 · [email protected]
湖北玖天生物医药科技有限公司027-88013699 17354350817 · [email protected]

추가 설명

정의ChEBI: A vinylarene that is benzene carrying a vinyl group. It has been isolated from the benzoin resin produced by Styrax species.

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