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Basic Description
| Synonyms | DTXSID40946352 | Fast Red B tetrafluoroborate salt, Dye content 95 % | Benzenediazonium, 2-methoxy-4-nitro-, tetrafluoroborate(1-) (1:1) | F77939 | EN300-12441196 | Fast Red B tetrafluoroborate salt | 2-Methoxy-4-nitrobenzene-1-diazonium tetrafluoridobora |
|---|---|
| Specifications & Purity | ≥95% |
| Storage Temp | Store at 2-8°C |
| Shipped In |
Wet ice This product requires cold chain shipping. Ground and other economy services are not available. |
| Product Description |
Fast Red B tetrafluoroborate salt is a diazonium stain with an absorption maximum of 375 nm. |
Taxonomic Classification
Taxonomy Tree
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Kingdom
Organic compounds
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Superclass
Benzenoids
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Class
Benzene and substituted derivatives
- Subclass Nitrobenzenes
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Class
Benzene and substituted derivatives
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Superclass
Benzenoids
| Kingdom | Organic compounds |
|---|---|
| Superclass | Benzenoids |
| Class | Benzene and substituted derivatives |
| Subclass | Nitrobenzenes |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Nitrophenyl ethers |
| Alternative Parents | Methoxyanilines Phenoxy compounds Nitroaromatic compounds Methoxybenzenes Diazonium tetrahaloborates Anisoles Alkyl aryl ethers Propargyl-type 1,3-dipolar organic compounds Organic oxoazanium compounds Organic metalloid salts Organic oxides Hydrocarbon derivatives Organic cations |
| Molecular Framework | Aromatic homomonocyclic compounds |
| Substituents | Nitrophenyl ether - Methoxyaniline - Phenoxy compound - Nitroaromatic compound - Diazonium tetrahaloborate - Anisole - Methoxybenzene - Phenol ether - Alkyl aryl ether - C-nitro compound - Organic diazonium salt - Organic nitro compound - Ether - Organic oxoazanium - Organic metalloid salt - Allyl-type 1,3-dipolar organic compound - Propargyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Organooxygen compound - Organonitrogen compound - Organic oxygen compound - Organic nitrogen compound - Organic oxide - Hydrocarbon derivative - Organic salt - Organic cation - Aromatic homomonocyclic compound |
| Description | This compound belongs to the class of organic compounds known as nitrophenyl ethers. These are aromatic compounds containing a nitrobenzene moiety that carries an ether group on the benzene ring. |
| External Descriptors | Not available |
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Names and Identifiers
| Pubchem Sid | 504768748 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/504768748 |
| IUPAC Name | 2-methoxy-4-nitrobenzenediazonium;tetrafluoroborate |
| INCHI | InChI=1S/C7H6N3O3.BF4/c1-13-7-4-5(10(11)12)2-3-6(7)9-8;2-1(3,4)5/h2-4H,1H3;/q+1;-1 |
| InChIKey | GYYABOARHFFQTR-UHFFFAOYSA-N |
| Smiles | [B-](F)(F)(F)F.COC1=C(C=CC(=C1)[N+](=O)[O-])[N+]#N |
| Isomeric SMILES | [B-](F)(F)(F)F.COC1=C(C=CC(=C1)[N+](=O)[O-])[N+]#N |
| WGK Germany | 3 |
| PubChem CID | 18628470 |
| Molecular Weight | 266.95 |
Certificates（CoA,COO,BSE/TSE and Analysis Chart)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Date | Item |
|---|---|---|---|
 L2206718 |
Certificate of Analysis | Oct 14, 2022 | F345603 |
| L2206742 |
Certificate of Analysis | Oct 14, 2022 | F345603 |
| L2206743 |
Certificate of Analysis | Oct 14, 2022 | F345603 |
Chemical and Physical Properties
| Solubility | Soluble in acetonitirile (1 mg/ml). |
|---|---|
| Melt Point(°C) | 122-124° C (lit.) |
| Molecular Weight | 266.950 g/mol |
| XLogP3 | |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 9 |
| Rotatable Bond Count | 1 |
| Exact Mass | 267.044 Da |
| Monoisotopic Mass | 267.044 Da |
| Topological Polar Surface Area | 83.200 Ų |
| Heavy Atom Count | 18 |
| Formal Charge | 0 |
| Complexity | 260.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 0 |
| Covalently-Bonded Unit Count | 2 |
Solution Calculators
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