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等級
technical grade
化驗
≥90%
形狀
solid
bp
274 °C/100 mmHg (lit.)
mp
38-40 °C (lit.)
密度
0.818 g/mL at 25 °C (lit.)
SMILES 字串
CCCCCCCCCCCCCCCCCC#N
InChI
1S/C18H35N/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19/h2-17H2,1H3
InChI 密鑰
RHSBIGNQEIPSCT-UHFFFAOYSA-N
一般說明
Stearonitrile undergoes W-6 Raney nickel catalyzed hydrogenation reaction. It forms inclusion complexes with urea.
應用
Stearonitrile was used to study the behaviour of dipalmitoylphosphatidylcholine mixed with stearonitrile at the air–water interface by surface pressure–area measurements and by direct visualisation of monolayers by Brewster angle microscopy. It was used to study the phase behaviour of stearic acid mixed with stearonitrile, in bulk and in a monolayer at the air–water interface.
訊號詞
Warning
危險聲明
危險分類
Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation
儲存類別代碼
11 - Combustible Solids
水污染物質分類（WGK）
WGK 3
閃點（°F）
235.4 °F - closed cup
閃點（°C）
113 °C - closed cup
個人防護裝備
dust mask type N95 (US), Eyeshields, Gloves
Rute I S Romão et al.
Chemistry and physics of lipids, 131(1), 27-39 (2004-06-24)
The behaviour of dipalmitoylphosphatidylcholine (DPPC), mixed with stearonitrile (SN), was investigated at the air-water interface by surface pressure-area (pi-A) measurements and by direct visualisation of monolayers by Brewster angle microscopy (BAM). The pi-A-X diagram of system DPPC/SN was compared with
A C T Teixeira et al.
Chemistry and physics of lipids, 144(2), 160-171 (2006-10-10)
The solid-liquid phase behaviour of stearic acid (SA) and stearonitrile (SN) in binary mixtures was investigated by differential scanning calorimetry (DSC), and the formation of SA-SN mixed monolayers at the air-water interface was followed by surface pressure-area (pi-A) measurements and
A CP-MAS NMR study of n-alkanes included in urea: conformational dependences of the substituent effects for n-substituted alkanes.
Okazaki M and McDowell CA.
Journal of Molecular Structure, 118(1), 149-156 (1984)
The preparation of Raney nickel catalysts and their use under conditions comparable with those for platinum and palladium catalysts.
Adkins H and Billica HR.
Journal of the American Chemical Society, 70(2), 695-698 (1948)
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