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线性分子式:
(CH3)2C(OCH3)2
化学文摘社编号:
分子量:
104.15
UNSPSC Code:
41116107
NACRES:
NA.02
PubChem Substance ID:
EC Number:
201-056-0
Beilstein/REAXYS Number:
635678
MDL number:
InChI
1S/C5H12O2/c1-5(2,6-3)7-4/h1-4H3
InChI key
HEWZVZIVELJPQZ-UHFFFAOYSA-N
SMILES string
COC(C)(C)OC
grade
analytical standard
vapor density
3.59 (vs air)
vapor pressure
60 mmHg ( 15.8 °C)
assay
≥99.4% (GC)
shelf life
limited shelf life, expiry date on the label
expl. lim.
31 %, 58 °F, 6 %, 27 °F
technique(s)
HPLC: suitable, gas chromatography (GC): suitable
Quality Level
refractive index
n20/D 1.378
bp
79-81 °C, 83 °C (lit.)
density
0.847 g/mL at 25 °C (lit.)
application(s)
environmental
format
neat
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相关类别
General description
2,2-Dimethoxypropane is an organic compound, which may be used as a protecting agent in the process of the synthesis of structurally related alkaloids like narciclasine and lycoricidine using phenylbromide as the starting material.
Application
2,2-Dimethoxypropane may be used as an analytical standard for the determination of the analyte in biological samples by headspace gas chromatography-mass spectrometry (HS-GC/MS) technique.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
signalword
Danger
hcodes
Hazard Classifications
Eye Irrit. 2 - Flam. Liq. 2 - Skin Irrit. 2
存储类别
3 - Flammable liquids
wgk
WGK 2
flash_point_f
14.0 °F - closed cup
flash_point_c
-10 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
法规信息
危险化学品
此项目有
Total Synthesis of Lycoricidine and Narciclasine by Chemical Dearomatization of Bromobenzene
Southgate.HE, et al.
Angewandte Chemie (Weinheim an der Bergstrasse, Germany), 129(47), 15245-15248 (2017)
Quantitative determination of n-propane, iso-butane, and n-butane by headspace GC-MS in intoxications by inhalation of lighter fluid
Bouche MPLA, et al.
Journal of Analytical Toxicology, 26(1), 35-42 (2002)
W Möller et al.
Biotechnic & histochemistry : official publication of the Biological Stain Commission, 69(5), 289-290 (1994-09-01)
We describe chemical dehydration with 2,2-dimethoxypropane (DMP) for rapid paraffin embedding using a mixture of DMP and mineral oil followed by mineral oil as clearing intermediates. This method is useful for classical histological techniques as well as for histochemistry and
Akito Takeuchi et al.
Biomedical chromatography : BMC, 24(5), 465-471 (2009-08-19)
A method for routinely determination of dimethyl sulfoxide (DMSO) and dimethyl sulfone (DMSO(2)) in human urine was developed using gas chromatography-mass spectrometry. The urine sample was treated with 2,2-dimethoxypropane (DMP) and hydrochloric acid for efficient removal of water, which causes
R Dierichs et al.
Histochemistry, 74(2), 263-269 (1982-01-01)
Dehydration with 2,2-dimethoxypropane acidified with 1 n HCl in an 1:100 volume ratio has been found to be unsuitable for the preservation of cell membranes in single cell preparations. Reducing the HCl concentration to 0.1 or 0.01 n results in
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