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166502

Sigma-Aldrich

Glyoxal sodium bisulfite addition compound hydrate

Synonym(s):

1,2-Dihydroxy-1,2-ethanedisulfonic acid disodium salt hydrate

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About This Item

Linear Formula:
[-CH(OH)SO3Na]2 · xH2O
CAS Number:
Molecular Weight:
266.16 (anhydrous basis)
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

form

solid

mp

193 °C (dec.) (lit.)

SMILES string

O.[Na+].[Na+].OC(C(O)S([O-])(=O)=O)S([O-])(=O)=O

InChI

1S/C2H6O8S2.2Na.H2O/c3-1(11(5,6)7)2(4)12(8,9)10;;;/h1-4H,(H,5,6,7)(H,8,9,10);;;1H2/q;2*+1;/p-2

InChI key

JQYGKJGYGOFFIK-UHFFFAOYSA-L

General description

Convenient, nonaqueous form of glyoxal

Application

Glyoxal sodium bisulfite addition compound hydrate was used to convert N-benzyl-2,3,4-trimethoxyaniline to sodium 5,6,7-trimethoxy-1-benzylindolyl-2-sulfite. It was used in the synthesis of 6-hydroxyquinoxaline.

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Mescaline Analogs. VIII. Substituted 5-Methoxy-and 5, 6, 7-Trimethoxyindoles.
Benington F, et al.
The Journal of Organic Chemistry, 23(1), 19-23 (1958)
404. Quinoxaline N-oxides. Part V. Further Bz-substituted derivatives.
Silk JA.
Journal of the Chemical Society, 2058-2063 (1956)

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