Substance
ID:181026
Names and Identifiers
IUPAC name
disodium 5-isothiocyanato-2-[(E)-2-(4-isothiocyanato-2-sulfonatophenyl)ethenyl]benzene-1-sulfonate
Synonyms
DIDSDisodium 4,4′-diisothiocyanatostilbene-2,2′-disulfonate4,4′-Diisothiocyanatostilbene-2,2′-disulfonic acid disodium salt hydrate
IUPAC Traditional name
disodium 5-isothiocyanato-2-[(E)-2-(4-isothiocyanato-2-sulfonatophenyl)ethenyl]benzenesulfonate
Registration numbers
Beilstein Number
MDL Number
PubChem SID
CAS Number
Properties
Safety Information
European Hazard Symbols
Harmful (Xn)GHS Hazard statements
H315-H319-H334-H335
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
Risk Statements
36/37/38-42
German water hazard class
3
GHS Pictograms
Respiratory sensitization, category 1
Germ cell mutagenicity, categories 1A,1B,2
Carcinogenicity, categories 1A,1B,2
Reproductive toxicity, categories 1A,1B,2
Specific Target Organ Toxicity – Single exposure, categories 1,2
Specific Target Organ Toxicity – Repeated exposure, categories 1,2
Aspiration Hazard, category 1
Acute toxicity (oral, dermal, inhalation), category 4
Skin irritation, category 2
Eye irritation, category 2
Skin sensitisation, category 1
Specific Target Organ Toxicity – Single exposure, category 3
Safety Statements
22-26
GHS Signal Word
Danger
GHS Precautionary statements
P261-P305+P351+P338-P342+P311
Storage Temperature
2-8°C
Physical Property
Apperance
yellow powder
Solubility
0.1 M potassium bicarbonate: soluble50 mg/mL
Product Information
Purity
≥80% (elemental analysis)
Molecule Details
Frequently Asked Questions
Live Chat and Frequently Asked Questions are available for this Product.
Application
A negatively charged homobifunctional cross-linking reagent. The isothiocyanate groups react with primary amines at pH 9.0-10.0.
Biochem/physiol Actions
A specific inhibitor of cellular anion permeability used in cell transport studies.
包装
1 g in poly bottle
25, 100, 250 mg in poly bottle
Live Chat and Frequently Asked Questions are available for this Product.
Application
A negatively charged homobifunctional cross-linking reagent. The isothiocyanate groups react with primary amines at pH 9.0-10.0.
Biochem/physiol Actions
A specific inhibitor of cellular anion permeability used in cell transport studies.
包装
1 g in poly bottle
25, 100, 250 mg in poly bottle
Molecular Spectra
No Data Available
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References
No Data Available
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