추천 제품
Grade
technical grade
분석
≥90%
형태
solid
bp
274 °C/100 mmHg (lit.)
mp
38-40 °C (lit.)
density
0.818 g/mL at 25 °C (lit.)
SMILES string
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 key
RHSBIGNQEIPSCT-UHFFFAOYSA-N
일반 설명
Stearonitrile undergoes W-6 Raney nickel catalyzed hydrogenation reaction. It forms inclusion complexes with urea.
애플리케이션
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.
신호어
Warning
유해 및 위험 성명서
Hazard Classifications
Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point (°F)
235.4 °F - closed cup
Flash Point (°C)
113 °C - closed cup
개인 보호 장비
dust mask type N95 (US), Eyeshields, Gloves
시험 성적서(COA)
제품의 로트/배치 번호를 입력하여 시험 성적서(COA)을 검색하십시오. 로트 및 배치 번호는 제품 라벨에 있는 ‘로트’ 또는 ‘배치’라는 용어 뒤에서 찾을 수 있습니다.
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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