트리옥틸포스핀 산화물
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트리옥틸포스핀 산화물 속성
- 녹는점
- 50-52 °C(lit.)
- 끓는 점
- 201-202 °C2 mm Hg(lit.)
- 밀도
- 0,88 g/cm3
- 증기압
- 0.004Pa at 50℃
- 인화점
- >230 °F
- 저장 조건
- Store below +30°C.
- 용해도
- <1g/L
- 물리적 상태
- 결정질 분말, 결정 또는 플레이크
- 색상
- 흰색에서 약간 노란색
- 수용성
- 불용성
- BRN
- 1796648
- 안정성
- 안정적인. 강한 산화제와 호환되지 않습니다.
- LogP
- 9.54
- CAS 데이터베이스
- 78-50-2(CAS DataBase Reference)
안전
- 위험 및 안전 성명
- 위험 및 사전주의 사항 (GHS)
위험품 표기 | Xi,Hazard | ||
---|---|---|---|
위험 카페고리 넘버 | 38-41-50/53-34 | ||
안전지침서 | 26-36/39-39-61-60-45-36/37/39 | ||
유엔번호(UN No.) | 3261 | ||
WGK 독일 | 2 | ||
RTECS 번호 | SZ1662500 | ||
자연 발화 온도 | 270 °C | ||
TSCA | Yes | ||
포장분류 | II | ||
HS 번호 | 29310095 | ||
HS 번호 | 32019090 | ||
독성 | LD50 orally in Rabbit: > 10000 mg/kg LD50 dermal Rat 2830 mg/kg | ||
기존화학 물질 | KE-34720 |
트리옥틸포스핀 산화물 C화학적 특성, 용도, 생산
화학적 성질
white crystalline powder용도
Trioctylphosphine oxide (TOPO) is most commonly used as the solvent due to its high boiling point and chemical stability, and its ability to prevent particle aggregation via coordination to the NP surface. trioctylphosphine oxide is a frequently used surfactant, starts to decompose at around 425°C.The industrial applications of trioctylphosphine oxide, make use of its complexing powers with metals and with hydrogen donor organic compounds. Commercial uses as a solvent extraction reagent are in the recovery of uranium from wet process phosphoric acid and in the recovery of byproduct acetic acid and furfural generated during sulphite wood pulping.
TOPO is a widely used chemical compound in nanocrystal synthesis, for the removal of heavy metals, and the removal of toxins in waste water. TOPO is often used as a ligand stabilizer for colloids in traditional thermal decomposition synthetic techniques.
trioctylphosphine oxide became a nearly irreplaceable solvent (mp 51-52°C) for high-temperature preparation of various type of nanocomposites. TOPO has a very high boiling point (411°C) which is an important prerequisite for the homogeneous nucleation and good crystallinity of the nanoparticles.
일반 설명
Visit our Sensor Applications portal to learn more.Purification Methods
Mason, McCarty and Peppard [J Inorg Nuclear Chem 24 967 1962] stirred a 0.1M solution in *benzene with an equal volume of 6M HCl at 40o in a sealed flask for 48hours, then washed the *benzene solution successively with water (twice), 5% aqueous Na2CO3 (three times) and water (six times). The *benzene and water were then evaporated under reduced pressure at room temperature. Zingaro and White [J Inorg Nucl Chem 12 315 1960] treated a pet ether solution with aqueous KMnO4 (to oxidise any phosphinous acids to phosphinic acids), then with sodium oxalate, H2SO4 and HCl (to remove any manganese compounds). The pet ether solution was slurried with activated alumina (to remove phosphinic acids), filtered, evaporated and the residue was recrystallised from pet ether or cyclohexane at -20o. It can also be recrystallised from EtOH. [Beilstein 4 IV 3466.]트리옥틸포스핀 산화물 준비 용품 및 원자재
원자재
준비 용품
트리옥틸포스핀 산화물 공급 업체
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