추천 제품
Quality Level
분석
≥98.0% (GC)
포함
~0.02% 2,6-di-tert-butyl-4-methylphenol as stabilizer
구성
5-hydroxy-1,3-dioxane, ~60%
4-hydroxymethyl-1,3-dioxolane, ~40%
refractive index
n20/D 1.451 (lit.)
n20/D 1.451
bp
192-193 °C (lit.)
density
1.203 g/mL at 25 °C (lit.)
작용기
ether
hydroxyl
SMILES string
OCC1COCO1.OC2COCOC2
InChI
1S/2C4H8O3/c5-4-1-6-3-7-2-4;5-1-4-2-6-3-7-4/h2*4-5H,1-3H2
InChI key
JIUMSISXCKWZTA-UHFFFAOYSA-N
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일반 설명
Glycerol formal (GF) is a light glycerol acetal that is composed of ~60% 5-hydroxy-1,3-dioxane and ~40% 4-hydroxymethyl-1,3-dioxolane. It can be prepared by reacting glycerol and formaldehyde in the presence of acid catalyst. The potential of GF as an injection solvent for use in toxicity testing has been reported.
애플리케이션
Glycerol formal is used to to solubilize water-insoluble compounds for subsequent aqueous dilution. It has been used as a chemical and dye emulsifier and as a cosolvent for drug delivery. Glycerol formal was used as a vehicle for antibiotic delivery in rats.
Glycerol formal may be used in the multi-step synthesis of 9-[(2-hydroxy-1-(hydroxymethyl)ethoxy)methyl]guanine (2′-nor-2′-deoxyguanosine), an analog of acyclovir. It may be used in the preparation of 4-substituted dioxolanes.
WGK
WGK 3
개인 보호 장비
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
이미 열람한 고객
4-Substituted dioxolanes by chemoselective reactions on glycerol formal.
Tetrahedron Letters, 34(27), 4335-4336 (1993)
Activation by thymidine kinase and potent antiherpetic activity of 2'-nor-2'-deoxyguanosine (2' NDG).
Biochemical and Biophysical Research Communications, 108(4), 1716-1721 (1982)
A note on glycerol formal as a solvent in toxicity testing.
The Journal of Pharmacy and Pharmacology, 11(1), 150-156 (1959)
Selective catalytic etherification of glycerol formal and solketal with dialkyl carbonates and K2CO3.
Green Chemistry, 14(1), 188-200 (2012)
Advances in pharmacological sciences, 2011, 608912-608912 (2011-12-14)
GABA(A) receptors containing α2/3 subunits are current targets in the battle to develop new pain medications, as they are expressed in the spinal cord where increasing inhibitory drive should result in analgesia. However, this approach is prone to a range
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