추천 제품
Grade
anhydrous
vapor density
3.04 (vs air)
vapor pressure
0.02 mmHg ( 36.4 °C)
분석
99%
불순물
<0.005% water
bp
243-244 °C/740 mmHg (lit.)
mp
35-38 °C (lit.)
density
1.321 g/mL at 25 °C (lit.)
SMILES string
O=C1OCCO1
InChI
1S/C3H4O3/c4-3-5-1-2-6-3/h1-2H2
InChI key
KMTRUDSVKNLOMY-UHFFFAOYSA-N
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교체됨
신호어
Warning
유해 및 위험 성명서
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2 - STOT RE 2 Oral
표적 기관
Kidney
Storage Class Code
11 - Combustible Solids
WGK
WGK 1
Flash Point (°F)
289.4 °F - closed cup
Flash Point (°C)
143 °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.
Niccolò Peruzzi et al.
The journal of physical chemistry. B, 116(49), 14398-14405 (2012-11-24)
The solubility of some potassium salts (KF, KCl, KBr, KI, KNO(3), KClO(4), KSCN, and KSeCN) in ethylene carbonate (EC) was determined at different temperatures with an inductively coupled plasma atomic emission spectrometer. From the solubility measurements, the thermodynamic parameters ΔG
O Hernández-Meléndez et al.
Bioresource technology, 100(2), 737-743 (2008-09-02)
The graft polymerization reaction between ethylene carbonate (EC) and scots pine sawdust (SPS) or peat moss (PM) offers a solvent-free approach to the simple and inexpensive aliphatic derivatization of these lignocellulosic fibers. This reaction was studied with liquid or vapor
Tan Winie et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 63(3), 677-684 (2005-09-15)
Fourier transform infrared (FT-IR) spectroscopic studies have been undertaken to investigate the interactions among components in a system of hexanoyl chitosan-lithium trifluoromethanesulfonate (LiCF(3)SO(3))-diethyl carbonate (DEC)/ethylene carbonate (EC). LiCF(3)SO(3) interacts with the hexanoyl chitosan to form a hexanoyl chitosan-salt complex that
Synthesis of dimethyl carbonate by transesterification of ethylene carbonate over activated dawsonites.
Georgiana Stoica et al.
ChemSusChem, 2(4), 301-304 (2009-02-07)
Sang-Jae Park et al.
Journal of the American Chemical Society, 137(7), 2565-2571 (2015-02-04)
Here we describe a class of electric-conducting polymers that conduct electrons via the side chain π-π stacking. These polymers can be designed and synthesized with different chemical moieties to perform different functions, extremely suitable as a conductive polymer binder for
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