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108790

Sigma-Aldrich

Glutaraldehyde sodium bisulfite addition compound

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About This Item

Linear Formula:
NaO3SCH(OH)(CH2)3CH(OH)SO3Na
CAS Number:
7420-89-5
Molecular Weight:
308.24
EC Number:
231-043-5
UNSPSC Code:
12352100
PubChem Substance ID:
24846828
NACRES:
NA.22

mp

>300 °C (lit.)

solubility

1 M NaOH: soluble 50 mg/mL, clear (colourless to dark yellow-orange)
1 M NaOH: soluble 50 mg/mL

SMILES string

OS(C(O)CCCC(O)S(O)(=O)=O)(=O)=O.[Na+].[Na+]

InChI

1S/C5H12O8S2.2Na/c6-4(14(8,9)10)2-1-3-5(7)15(11,12)13;;/h4-7H,1-3H2,(H,8,9,10)(H,11,12,13);;/q;2*+1/p-2

InChI key

YGZZDQOCTFVBFC-UHFFFAOYSA-L

Application

Glutaraldehyde may be used as a cross-linking reagent.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H317

Hazard Classifications

Skin Irrit. 2 - Skin Sens. 1

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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H Fan et al.
International journal of pharmaceutics, 213(1-2), 103-116 (2001-02-13)
Doxorubicin is one of the most potent anti-tumor agents used generally in the treatment of bone cancer. Like other cancer chemotharepeutics, it produces undesirable side effects such as cardiotoxicity, which is especially severe when administrated via the conventional intravenous route.

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