추천 제품
Grade
anhydrous
Quality Level
vapor density
4.5 (vs air)
vapor pressure
1 mmHg ( 25.6 °C)
분석
≥99%
형태
liquid
autoignition temp.
559 °F
expl. lim.
0.34-6.3 %
불순물
<0.005% water
증발 잔류물
<0.0005%
refractive index
n20/D 1.418 (lit.)
bp
156-157 °C (lit.)
mp
−52 °C (lit.)
density
0.814 g/mL at 25 °C (lit.)
SMILES string
CCCCCCO
InChI
1S/C6H14O/c1-2-3-4-5-6-7/h7H,2-6H2,1H3
InChI key
ZSIAUFGUXNUGDI-UHFFFAOYSA-N
유사한 제품을 찾으십니까? 방문 제품 비교 안내
일반 설명
1-Hexanol is a linear primary alcohol. It is formed as an intermediate during the catalytic transformation of cellulose. The ability of 1,1,3,3-tetramethylguanidine (TMG) in 1-hexanol solvent system to capture carbon dioxide has been assessed. The solubility of light fullerenes in 1-hexanol as a function of temperature and pressure was studied.
1-Hexanol is produced from coconut oil and palm oils. It is used in the production of antiseptics, fragrances and perfumes. 1-Hexanol is also used as a solvent in the production of plasticizers.
애플리케이션
1-Hexanol has been used as an odorant to study olfactory responses and to thin the dielectric layer of poly(4-vinylphenol) (PVP).
신호어
Warning
유해 및 위험 성명서
Hazard Classifications
Acute Tox. 4 Dermal - Acute Tox. 4 Oral - Eye Irrit. 2 - Flam. Liq. 3
Storage Class Code
3 - Flammable liquids
WGK
WGK 1
Flash Point (°F)
140.0 °F - closed cup
Flash Point (°C)
60 °C - closed cup
개인 보호 장비
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
이미 열람한 고객
A 4-dimensional representation of antennal lobe output based on an ensemble of characterized projection neurons
Journal of Neuroscience Methods, 180(2), 208-223 (2009)
Patty's Toxicology (2012)
Kinetics of carbon dioxide binding by 1,1,3,3-tetramethylguanidine in 1-hexanol.
International Journal of Greenhouse Gas Control, 26, 76-82 (2014)
Pressure dependence of the solubility of light fullerenes in 1-hexanol from 298.15 K to 363.15 K.
Journal of Molecular Liquids, 209, 71-76 (2015)
Direct catalytic conversion of cellulose to liquid straight-chain alkanes.
Energy & Environmental Science, 8(1), 230-240 (2015)
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