Sign In to View Organizational & Contract Pricing.
Select a Size
About This Item
Linear Formula:
(HC(O)C(O)H)3 · 2H2O
CAS Number:
Molecular Weight:
210.14
EC Number:
224-551-3
UNSPSC Code:
12352100
PubChem Substance ID:
Beilstein/REAXYS Number:
3542160
MDL number:
InChI key
BDSPTFQIOAEIII-UHFFFAOYSA-N
InChI
1S/C6H10O8/c7-1-2(8)12-6-5(11-1)13-3(9)4(10)14-6/h1-10H
SMILES string
[H]O[H].[H]O[H].OC1OC2OC(O)C(O)OC2OC1O
assay
≥97%
Looking for similar products? Visit Product Comparison Guide
Application
Reactant involved in the synthesis of:
- Aza-analogs of 1,4-naphthoquinones as effectors of plasmodial thioredoxin and glutathione reductase
- Substituted side-bridged cyclam derivatives
- Furandicarboxylic acid di-methyl ester derivatives
Other Notes
This form of glyoxal is composed of 3 moles of glyoxal and 2 moles of water in a relatively stable configuration.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - Skin Sens. 1
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
>239.0 °F
flash_point_c
> 115 °C
ppe
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
新产品
This item has
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service