추천 제품
Quality Level
분석
97%
형태
liquid
refractive index
n20/D 1.432 (lit.)
bp
200-204 °C (lit.)
density
0.88 g/mL at 25 °C (lit.)
SMILES string
CCCCCCCCN=C=O
InChI
1S/C9H17NO/c1-2-3-4-5-6-7-8-10-9-11/h2-8H2,1H3
InChI key
DYQFCTCUULUMTQ-UHFFFAOYSA-N
일반 설명
Octyl isocyanate was reported to inactivate serine proteinase, chymotrypsin.
애플리케이션
Octyl isocyanate was used to suppress side reactions such as backbiting or chain transfer reaction during polymerization reactions. It was also used in the synthesis of:
- low molar mass organogelator containing 2-(2′-hydroxyphenyl)benzoxazole (HPB) unit with long alkyl chain
- N-octylurea
- N-cyclopropyl-N′-octylurea
신호어
Danger
유해 및 위험 성명서
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2 - Resp. Sens. 1 - Skin Irrit. 2 - Skin Sens. 1 - STOT SE 3
표적 기관
Respiratory system
Storage Class Code
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
WGK
WGK 3
Flash Point (°F)
159.8 °F - closed cup
Flash Point (°C)
71 °C - closed cup
개인 보호 장비
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
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.
이미 열람한 고객
W E Brown et al.
Science (New York, N.Y.), 174(4009), 608-610 (1971-11-05)
Alkyl isocyanates react specifically with the two serine proteinases, chymotrypsin and elastase, to yield inactive enzyme derivatives containing 1 male of reagent per mole of enzyme. Octyl isocyanate inactivates chymotrypsin only, while butyl isocyanate inactivates both enzymes but shows greater
Tae Hyeon Kim et al.
Journal of nanoscience and nanotechnology, 10(10), 6929-6933 (2010-12-09)
A low molar mass organogelator 1 containing 2-(2'-hydroxyphenyl)benzoxazole (HPB) unit with long alkyl chain was synthesized by the reaction with HPB and octyl isocyanate in THF at room temperature. A new chelate-based organogelator 1-Zn(II) was prepared with the reaction of
C Morisseau et al.
Chemical research in toxicology, 14(4), 409-415 (2001-04-17)
The microsomal epoxide hydrolase (mEH) plays a significant role in the metabolism of xenobiotics such as polyaromatic toxicants. Additionally, polymorphism studies have underlined a potential role of this enzyme in relation to several diseases, such as emphysema, spontaneous abortion, and
Anionic polymerization of isocyanates with optical functionalities.
Shin YD, et al.
Polymer, 42(19), 7979-7985 (2001)
Isocyanate binding to yeast glutathione reductase measured by fluorescence spectroscopy.
K J Baylor et al.
Biochemical Society transactions, 25(1), 47S-47S (1997-02-01)
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