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About This Item
Empirical Formula (Hill Notation):
C6H8O3
CAS Number:
Molecular Weight:
128.13
UNSPSC Code:
12162002
NACRES:
NA.23
PubChem Substance ID:
EC Number:
224-020-6
Beilstein/REAXYS Number:
114457
MDL number:
assay
98%
bp
180-182 °C/25 mmHg (lit.)
mp
42-46 °C (lit.)
SMILES string
CC1CC(=O)OC(=O)C1
InChI
1S/C6H8O3/c1-4-2-5(7)9-6(8)3-4/h4H,2-3H2,1H3
InChI key
MGICRVTUCPFQQZ-UHFFFAOYSA-N
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
235.4 °F - closed cup
flash_point_c
113 °C - closed cup
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Atsushi Harada et al.
Journal of biomaterials science. Polymer edition, 28(10-12), 1025-1035 (2017-04-27)
The properties of stimuli-responsive polymers change significantly with changes to their environment, such as temperature and pH. This behavior can be utilized for the preparation of stimuli-responsive carriers for efficient cytosolic delivery of active drugs. Among the possible environmental conditions
Peter A Beckmann et al.
Solid state nuclear magnetic resonance, 85-86, 1-11 (2017-03-07)
We report a variety of experiments and calculations and their interpretations regarding methyl group (CH
Maiko Miyazaki et al.
Bioconjugate chemistry, 29(1), 44-55 (2017-12-01)
For the enhancement of therapeutic effects and reduction of side effects derived from anticancer drugs in cancer chemotherapy, it is imperative to develop drug delivery systems with cancer-specificity and controlled release function inside cancer cells. pH-sensitive liposomes are useful as
Global Trade Item Number
| SKU | GTIN |
|---|---|
| M47809-5G | 04061833015841 |
| M47809-25G | 04061833015834 |
