GLUTARALDEHYDE BIS SODIUM BISULFITE
Glutaraldehyde sodium bisulfite addition compound
CAS: 28959-35-5
Molecular Formula: C5H10O8S2.2Na
GLUTARALDEHYDE BIS SODIUM BISULFITE - Names and Identifiers
GLUTARALDEHYDE BIS SODIUM BISULFITE - Physico-chemical Properties
| Molecular Formula | C5H10O8S2.2Na |
| Molar Mass | 308.24 |
| Melting Point | >300°C(lit.) |
| Appearance | solid |
GLUTARALDEHYDE BIS SODIUM BISULFITE - Risk and Safety
| Safety Description | 24/25 - Avoid contact with skin and eyes. |
| WGK Germany | 3 |
GLUTARALDEHYDE BIS SODIUM BISULFITE - Introduction
Glutaraldehyde sodium bisulfite addition compound is an organic compound with the chemical formula C5H7NO2 · NaHSO3. The following is a description of its nature, use, formulation and safety information:
Nature:
- Glutaraldehyde sodium bisulfite addition compound has the appearance of a white crystalline powder.
-It can be dissolved in water and is weakly acidic in water.
-Its melting point is about 220 ° C.
-Stable in a dry environment, but will decompose in a humid environment.
Use:
- Glutaraldehyde sodium bisulfite addition compound is widely used in the fields of medicine and biochemistry.
-It is a germicide and disinfectant that can kill bacteria, viruses and fungi.
-Because of its bactericidal effect, it is often used for disinfection and sterilization of medical equipment.
-It can also be used to prepare deoxynucleic acid (DNA) and protein samples, and to fix cells and tissues.
Method:
- Glutaraldehyde sodium bisulfite addition compound is usually prepared by mixing glutamaldehyde and sodium sulfite in a certain proportion, and reacting to generate the compound.
Safety Information:
- Glutaraldehyde sodium bisulfite addition compound is a corrosive substance that may cause irritation and damage when in contact with skin and eyes.
-When in use, take appropriate personal protective measures, such as wearing protective gloves, safety glasses and protective masks.
-Avoid inhaling its dust to avoid respiratory irritation and injury.
-should be stored in a dry, well-ventilated place, away from combustibles and oxidants.
-At disposal, follow local waste disposal regulations.
Nature:
- Glutaraldehyde sodium bisulfite addition compound has the appearance of a white crystalline powder.
-It can be dissolved in water and is weakly acidic in water.
-Its melting point is about 220 ° C.
-Stable in a dry environment, but will decompose in a humid environment.
Use:
- Glutaraldehyde sodium bisulfite addition compound is widely used in the fields of medicine and biochemistry.
-It is a germicide and disinfectant that can kill bacteria, viruses and fungi.
-Because of its bactericidal effect, it is often used for disinfection and sterilization of medical equipment.
-It can also be used to prepare deoxynucleic acid (DNA) and protein samples, and to fix cells and tissues.
Method:
- Glutaraldehyde sodium bisulfite addition compound is usually prepared by mixing glutamaldehyde and sodium sulfite in a certain proportion, and reacting to generate the compound.
Safety Information:
- Glutaraldehyde sodium bisulfite addition compound is a corrosive substance that may cause irritation and damage when in contact with skin and eyes.
-When in use, take appropriate personal protective measures, such as wearing protective gloves, safety glasses and protective masks.
-Avoid inhaling its dust to avoid respiratory irritation and injury.
-should be stored in a dry, well-ventilated place, away from combustibles and oxidants.
-At disposal, follow local waste disposal regulations.
Last Update：2024-04-09 21:04:16
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GLUTARALDEHYDE BIS SODIUM BISULFITE
Bis(2-ethylhexyl) maleate
DIETHYL 1-AMINO-3-METHYL-1H-PYRROLE-2,4-DICARBOXYLATE
SULFOSUCCINIMIDYL-TRANS-4-(N-MALEIMIDOMETHYL)CYCLOHEXANE-1-CARBOXYLATE
1-Propanol, 3-[(12-cyclohexyldodecyl)oxy]-2-(phenylmethoxy)-
2-[3-Methyl-4(2,2,2-trifluoroethoxy)pyrid-2yl]-Methylthio]benzimidazole
(5-CHLORO-THIOPHEN-2-YL)-CARBAMIC ACID TERT-BUTYL ESTER
3-(BOC-氨基)环己基羧酸
4-[(2-aminophenyl)methyl]-2,6-diisopropylaniline
2-(2,6-DICHLOROPHENOXY)ACETYL CHLORIDE
Bis(2-ethylhexyl) maleate
DIETHYL 1-AMINO-3-METHYL-1H-PYRROLE-2,4-DICARBOXYLATE
SULFOSUCCINIMIDYL-TRANS-4-(N-MALEIMIDOMETHYL)CYCLOHEXANE-1-CARBOXYLATE
1-Propanol, 3-[(12-cyclohexyldodecyl)oxy]-2-(phenylmethoxy)-
2-[3-Methyl-4(2,2,2-trifluoroethoxy)pyrid-2yl]-Methylthio]benzimidazole
(5-CHLORO-THIOPHEN-2-YL)-CARBAMIC ACID TERT-BUTYL ESTER
3-(BOC-氨基)环己基羧酸
4-[(2-aminophenyl)methyl]-2,6-diisopropylaniline
2-(2,6-DICHLOROPHENOXY)ACETYL CHLORIDE