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品質水準
アッセイ
98%
形状
liquid
屈折率
n20/D 1.3 (lit.)
bp
97 °C (lit.)
密度
1.871 g/mL at 25 °C (lit.)
SMILES記法
FC(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)Br
InChI
1S/C6BrF13/c7-5(16,17)3(12,13)1(8,9)2(10,11)4(14,15)6(18,19)20
InChI Key
JTYRBFORUCBNHJ-UHFFFAOYSA-N
アプリケーション
Employed in the preparation of perfluorononanal by hydroformylation.
シグナルワード
Warning
危険有害性情報
危険有害性の分類
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
ターゲットの組織
Respiratory system
保管分類コード
10 - Combustible liquids
WGK
WGK 3
引火点(°F)
Not applicable
引火点(℃)
Not applicable
個人用保護具 (PPE)
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
試験成績書（COA）
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Intra-abdominal sepsis and perfluorocarbons: mechanism of protection.
D B Hoyt et al.
Current surgery, 39(3), 165-167 (1982-05-01)
Douglass et al.
The Journal of organic chemistry, 65(5), 1434-1441 (2000-05-18)
A triphenylsilyl group is used as an auxiliary in the synthesis of heterodisubstituted p-carboranes via triphenylsilyl-p-carborane (1). The preparation of 1 is statistical, but with recovery of the starting p-carborane, the effective conversion to 1 is about 90%. Carborane 1
S L Wootton et al.
AJR. American journal of roentgenology, 161(2), 409-416 (1993-08-01)
The disadvantages of water-soluble gastrointestinal contrast agents include high osmolality, contrast dilution, and severe toxicity if aspirated. Perfluorocarbons are nontoxic in the lung and peritoneal cavity. Because perfluorocarbons are immiscible with water, they have no osmotic effect and cannot be
Zhang Feng et al.
Angewandte Chemie (International ed. in English), 54(4), 1270-1274 (2014-12-04)
An efficient palladium-catalyzed Heck-type reaction of fluoroalkyl halides, including perfluoroalkyl bromides, trifluoromethyl iodides, and difluoroalkyl bromides, has been developed. The reaction proceeds under mild reaction conditions with high efficiency and broad substrate scope, and provides a general and straightforward access
M Scrime et al.
Journal of pharmaceutical sciences, 70(11), 1199-1201 (1981-11-01)
Beagle dogs received single perfluorohexyl bromide doses, either 30.2 g/kg po or 3.8 g/kg intratracheally. The apparent first-order plasma half-life during the terminal elimination phase was approximately 8 hr after oral treatment and greater than 8 hr after intratracheal administration.
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