Basic information
- Standard SMILES
N#[N+]c1ccc(Nc2ccccc2)cc1.O=S(=O)([O-])O- InChIKey
FMRQRWPEQSPSDG-UHFFFAOYSA-M- Molecular formula
- C12H11N3O4S
- Average molar mass
- 293.3 g/mol
- Monoisotopic mass
- 293.04702683
Names & identifiers
- Preferred name
- Benzenediazonium, 4-(phenylamino)-, sulfate (1:1)
- IUPAC
- 4-anilinobenzenediazonium;hydrogen sulfate
- English name
- 4-Diazodiphenylamine sulfate
- Molecular formula
- C12H11N3O4S
- Molecular weight
- 293.3
Names & synonyms
Show more names
Database identifiers
- CAS
4477-28-5- PubChem CID
- 78231
- DTXSID
DTXSID0063490- EC Number
- 224-756-8
Properties
Computed structural properties
- Topological polar surface area
- 126 Ų
- Hydrogen bond donors
- 2
- Hydrogen bond acceptors
- 6
- Rotatable bonds
- 2
- Heavy atoms
- 20
- Formal charge
- 0
- Complexity
- 304
Physicochemical properties
- Boiling point
- 623.17 ℃[at · 623.17℃[at 101 325 Pa]
- Density
- 1.512 · 1.512[at 20℃]
- vapor pressure
- 0 Pa · 0Pa at 25℃
- solubility
- 1 M · 1 M HCl: 10 mg/mL
- form
- solid
- Colour Index
- 37240 · 37240
- Water Solubility
- 21.24 g/L · 21.24g/L at 20℃
- Major Application
- diagnostic assay manufacturinghematologyhistology
- InChI
- 1S/C12H10N3.H2O4S/c13-15-12-8-6-11(7-9-12)14-10-4-2-1-3-5-10;1-5(2,3)4/h1-9,14H;(H2,1,2,3,4)/q+1;/p-1
- InChIKey
- FMRQRWPEQSPSDG-UHFFFAOYSA-M
- SMILES
- OS([O-])(=O)=O.N#[N+]c1ccc(Nc2ccccc2)cc1
- LogP
- 1.28 at · 1.28 at 23℃
- CAS DataBase Reference
- 4477 · 4477-28-5(CAS DataBase Reference)
- EPA Substance Registry System
- 4 · Benzenediazonium, 4-(phenylamino)-, sulfate (1:1) (4477-28-5)
- UNSPSC Code
- 12171500 · 12171500
- NACRES
- 47 · NA.47
- Symbol(GHS)
- 5 · GHS05,GHS08,GHS09
- Signal word
- Danger
- Hazard statements
- 315 · H315-H318-H341-H400
- Precautionary statements
- 202 · P202-P273-P280-P302+P352-P305+P351+P338-P308+P313
- PPE
- 95 · Eyeshields, Gloves, type N95 (US)
- WGK Germany
- 3 · 3
- TSCA
- TSCA listed
- HS Code
- 2927 · 2927.00.5000
- Storage Class
- 11 · 11 - Combustible Solids
- Hazard Classifications
- 1 Eye · Aquatic Acute 1Eye Dam. 1Muta. 2Skin Irrit. 2
- REACH Registrations
- Active
Safety & regulation
GHS classification
GHS Classification
Danger
H301 (66.7%): Toxic if swallowed [Danger Acute toxicity, oral]
P203, P264, P264+P265, P270, P273, P280, P301+P316, P302+P352, P305+P354+P338, P317, P318, P321, P330, P332+P317, P362+P364, P391, P405, and P501 (click each P-code to see the statement)
Aggregated GHS information provided per 3 reports by companies from 2 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
Hazard information
Regulatory Information
REACH registered substance: 4-anilinobenzenediazonium hydrogen sulphate (EC: 224-756-8)
Benzenediazonium, 4-(phenylamino)-, sulfate (1:1): Does not have an individual approval but may be used under an appropriate group standard
Safety data
- PPE
- Eyeshields, Gloves, type N95 (US)
- wgk
- 3
- tsca
- TSCA listed
- hs_code
- 2927.00.5000
- Signal word
- Danger
- Symbol(GHS)
- GHS05,GHS08,GHS09
- Storage Class
- 11 - Combustible Solids
- Hazard statements
- H315-H318-H341-H400
- REACH Registrations
- Active
- Hazard Classifications
- Aquatic Acute 1Eye Dam. 1Muta. 2Skin Irrit. 2
- Precautionary statements
- P202-P273-P280-P302+P352-P305+P351+P338-P308+P313
Chemistry & industry
Uses & manufacturing
Applications
Uses4-Aminodiphenylamine sulfate (Variamine Blue RT sulfate) is a multifunctional dye. Dyes are important tools in biological experiments. They can help researchers observe and analyze cell structures, track biomolecules, evaluate cell functions, distinguish cell types, detect biomolecules, study tissue pathology and monitor microorganisms. Their applications range from basic scientific research to clinical A wide range of diagnostics. Dyes are also widely used in traditional fields such as textile dyeing, as well as in emerging fields such as functional textile processing, food pigments and dye-sensitized solar cells.
Upstream & downstream products
Upstream raw materials
Suppliers50 total
Related reactions
No reaction records under the current filter.
Linked notes
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