推荐产品
等級
spectrophotometric grade
蒸汽密度
2.48 (vs air)
蒸汽壓力
26.98 psi ( 55 °C)
8.4 psi ( 20 °C)
化驗
≥99%
形狀
liquid
自燃溫度
500 °F
expl. lim.
~8.3 %
技術
UV/Vis spectroscopy: suitable
雜質
<0.010% water
蒸發殘留物
<0.0003%
折射率
n20/D 1.358 (lit.)
bp
35-36 °C (lit.)
mp
−130 °C (lit.)
密度
0.626 g/mL at 25 °C (lit.)
&lambda ；
H2O reference
紫外吸收
λ: 195 nm Amax: 1.00
λ: 200 nm Amax: 0.60
λ: 210 nm Amax: 0.30
λ: 220 nm Amax: 0.06
λ: 245-400 nm Amax: 0.01
SMILES 字串
CCCCC
InChI
1S/C5H12/c1-3-5-4-2/h3-5H2,1-2H3
InChI 密鑰
OFBQJSOFQDEBGM-UHFFFAOYSA-N
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一般說明
Pentane (n-pentane) undergoes hydroisomerization in the presence of nanocrystalline beta (BEA) zeolite. It has been reported as one of the products formed from the peroxidation of unsaturated fatty acid. It isomerizes to iso-pentane in the presence of ZSM-5 (Zeolite Socony Mobil-5) zeolite catalysts under hydrogen and nitrogen atmosphere.
Pentane is a low boiling solvent, which finds applications in industries as a petroleum solvent and as a substitute for diethyl ether.
Pentane is a low boiling solvent, which finds applications in industries as a petroleum solvent and as a substitute for diethyl ether.
訊號詞
Danger
危險分類
Aquatic Chronic 2 - Asp. Tox. 1 - Flam. Liq. 2 - STOT SE 3
標靶器官
Central nervous system
安全危害
儲存類別代碼
3 - Flammable liquids
水污染物質分類（WGK）
WGK 2
閃點（°F）
-40.0 °F
閃點（°C）
-40 °C
其他客户在看
Smallwood.McN I et al.
Solvent Recovery Handbook (2002)
Assessment of lipid peroxidation in newborn infants and rabbits by measurements of expired ethane and pentane: influence of parenteral lipid infusion.
Wispe JR, et al.
Pediatric Research, 19(4), 374-379 (1985)
Hydroisomerization of n-pentane over hybrid catalysts containing a supported hydrogenation catalyst.
Fujimoto K, et al.
Applied Catalysis A: General, 91(2), 81-86 (1992)
Hydroisomerization of pentane, hexane, and heptane for improving the octane number of gasoline.
Chica A and Corma A.
J. Catal., 187(1), 167-176 (1999)
Keisuke Maruyama et al.
Bioorganic & medicinal chemistry letters, 20(22), 6661-6666 (2010-10-05)
We have proposed a multi-template approach for drug development, focusing on similar fold structures of proteins, and have effectively generated lead compounds for several drug targets. Modification of these polypharmacological lead compounds is then needed to generate target-selective compounds. In
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