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线性分子式:
(C2H5O)2P(O)NCO
化学文摘社编号:
分子量:
179.11
UNSPSC Code:
12352100
PubChem Substance ID:
MDL number:
InChI
1S/C5H10NO4P/c1-3-9-11(8,6-5-7)10-4-2/h3-4H2,1-2H3
SMILES string
CCOP(=O)(OCC)N=C=O
InChI key
BSCBJDQIQBYMBT-UHFFFAOYSA-N
assay
96%
form
liquid
refractive index
n20/D 1.416 (lit.)
bp
85-87 °C/10 mmHg (lit.)
density
1.165 g/mL at 25 °C (lit.)
General description
Diethoxyphosphinyl isocyanate is an isocyanate derivative. It has been investigated for its performance as film forming electrolyte additive in propylene carbonate (PC) and EC/EMC-based electrolytes.
signalword
Danger
Hazard Classifications
Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Eye Irrit. 2 - Flam. Liq. 3 - Resp. Sens. 1 - Skin Irrit. 2 - Skin Sens. 1 - STOT SE 3
target_organs
Respiratory system
存储类别
3 - Flammable liquids
wgk
WGK 3
flash_point_f
118.4 °F - closed cup
flash_point_c
48 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
法规信息
新产品
此项目有
Isocyanate compounds as electrolyte additives for lithium-ion batteries.
Korepp C, et al.
Journal of Power Sources, 174(2), 387-393 (2007)
G Brigden et al.
European journal of nuclear medicine, 16(11), 795-799 (1990-01-01)
A new, single bolus method of in vivo blood pool imaging using a technetium Tc99m phosphine isocyanide complex (DEPIC) which binds to pre-albumin was evaluated in volunteers (n = 4) and patients (n = 20). DEPIC was assessed for its
M Nehéz et al.
Ecotoxicology and environmental safety, 17(2), 258-263 (1989-04-01)
Phenyl isocyanate (I) and diethoxyphosphoryl isocyanate (II), used as intermediates in organic chemical syntheses, were tested for their acute toxic, cytogenetic, and embryotoxic activity on mice of different strains. The oral LD50 values for male CFLP mice were determined to
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