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この商品について
化学式:
CH2=CHC(CH3)=CH2
CAS番号:
分子量:
68.12
EC Number:
201-143-3
UNSPSC Code:
12352100
PubChem Substance ID:
Beilstein/REAXYS Number:
969158
MDL number:
製品名
イソプレン, ≥99%
InChI key
RRHGJUQNOFWUDK-UHFFFAOYSA-N
InChI
1S/C5H8/c1-4-5(2)3/h4H,1-2H2,3H3
SMILES string
CC(=C)C=C
vapor density
2.35 (vs air)
vapor pressure
8.82 psi ( 20 °C)
assay
≥99%
form
liquid
autoignition temp.
428 °F
contains
100-150 ppm p-tert-butylcatechol as inhibitor
expl. lim.
10 %
refractive index
n20/D 1.422 (lit.)
bp
34 °C (lit.)
mp
−146 °C (lit.)
density
0.681 g/mL at 25 °C (lit.)
storage temp.
2-8°C
Quality Level
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Application
イソプレンは開始剤としてsec-ブチルリチウムの存在下、スチレンとの逐次アニオン重合による非対称のポリスチレン-ブロック-ポリイソプレン(PS-b-PI)ジブロック共重合体の合成に使用することができます。
Packaging
通い容器のオプションをご覧ください。
signalword
Danger
hcodes
Hazard Classifications
Aquatic Chronic 3 - Carc. 1B - Flam. Liq. 1 - Muta. 2
保管分類
3 - Flammable liquids
wgk
WGK 3
flash_point_f
-65.2 °F - closed cup
flash_point_c
-54 °C - closed cup
Morphology and elasticity of polystyrene-block-polyisoprene diblock copolymers in the melt.
Haenelt TG, et al.
Korea-Australia Rheology Journal, 26(3), 263-275 (2014)
H Koc et al.
Journal of breath research, 5(3), 037102-037102 (2011-06-10)
Isoprene is one of the most abundant endogenous volatile organic compounds (VOCs) contained in human breath and is considered to be a potentially useful biomarker for diagnostic and monitoring purposes. However, neither the exact biochemical origin of isoprene nor its
Russell K Monson et al.
The New phytologist, 195(3), 541-559 (2012-06-29)
The leaves of many plants emit isoprene (2-methyl-1,3-butadiene) to the atmosphere, a process which has important ramifications for global and regional atmospheric chemistry. Quantitation of leaf isoprene emission and its response to environmental variation are described by empirically derived equations
Michaela Stieglmeier et al.
International journal of systematic and evolutionary microbiology, 64(Pt 8), 2738-2752 (2014-06-08)
A mesophilic, neutrophilic and aerobic, ammonia-oxidizing archaeon, strain EN76(T), was isolated from garden soil in Vienna (Austria). Cells were irregular cocci with a diameter of 0.6-0.9 µm and possessed archaella and archaeal pili as cell appendages. Electron microscopy also indicated
Tomohisa Kuzuyama
Bioscience, biotechnology, and biochemistry, 66(8), 1619-1627 (2002-10-02)
Isoprenoids are synthesized by consecutive condensations of their five-carbon precursor, isopentenyl diphosphate, to its isomer, dimethylallyl diphosphate. Two pathways for these precursors are known. One is the mevalonate pathway, which operates in eucaryotes, archaebacteria, and cytosols of higher plants. The
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