CAS Number842-15-9
Synonyms7-amino-1,3-naphthalenedisulfonic acid monopotassium salt; EINECS 212-669-8; MFCD00064177
Molecular FormulaC10H8KNO6S2
Molecular Weight341.40200
Density0.881 g/mL at 25 °C(lit.)
Boiling Point159-161 °C(lit.)
Melting Point−69 °C(lit.)
Appearancewhite solid
| Chemical & Physical Properties | |
|---|---|
| CAS Number | 842-15-9 |
| Catalog No. | 2A-2197989 |
| Chinese Name | 7-氨基-1,3-萘二磺酸单钾盐 水合物 |
| Synonyms | 7-amino-1,3-naphthalenedisulfonic acid monopotassium salt; EINECS 212-669-8; MFCD00064177 |
| Molecular Formula | C10H8KNO6S2 |
| Molecular Weight | 341.40200 |
| Density | 0.881 g/mL at 25 °C(lit.) |
| Boiling Point | 159-161 °C(lit.) |
| Melting Point | −69 °C(lit.) |
| Appearance | white solid |
| Water Solubility | Insoluble |
| Storage Condition | avoid light |
| Application | Potassium 2-naphthylamine-6,8-disulfonate is a chemical that can be used to prepare dyes, medicines, pesticides, etc. [1]. |
| HTC | 2921450090 |
| Bioactivity | 2-Naphthylamine-6,8-disulfonic acid potassium is chemical that can be used for preparing dyestuff, medicine, agricultural chemicals etc[1]. Related Catalog Signaling Pathways >> Others >> Others Research Areas >> Inflammation/Immunology In Vitro 2-Naphthylamine-6,8-disulfonic acid potassium (compound 20) can inhibit human immunodeficiency virus HIV-1 and HIV-2 by 11% and 13.6% at a concentration of 1369 μM, respectively[1]. 2-Naphthylamine-6,8-disulfonic acid potassium (ANDS) can directly analyze polyglycolic pyrophosphate-linked oligosaccharides in cell cultures and tissues[3]. Guidelines (Following is our recommended protocol. This protocol only provides a guideline, and should be modified according to your specific needs).Labeling oligosaccharides[3]: 1. Prepared 0.15 M ANDS with 15% (v/v) acetic acid. 2. Prepare 1M solution of sodium cyanoborohydride in dimethyl sulfoxide (DMSO). 3. Add 5 μL ANDS reagent (1 μL if sample is below 200 pmol) to the sample. 4. Add 5 μL sodium cyanoborohydride solution (1 μL if sample is below 200 pmol) to the sample. 5. After mixing, the reaction was briefly centrifuged and allowed to dry for 18 hours at 37 °C. References [1]. G T Tan, et al. Potential anti-AIDS naphthalenesulfonic acid derivatives. Synthesis and inhibition of HIV-1 induced cytopathogenesis and HIV-1 and HIV-2 reverse transcriptase activities. J Med Chem. 1992 Dec 25;35(26):4846-53. [2]. K B Lee, et al. A new method for sequencing linear oligosaccharides on gels using charged, fluorescent conjugates. Carbohydr Res. 1991 Jul 18;214(1):155-68. [3]. Ningguo Gao, et al. Fluorophore-assisted carbohydrate electrophoresis: a sensitive and accurate method for the direct analysis of dolichol pyrophosphate-linked oligosaccharides in cell cultures and tissues. Methods. 2005 Apr;35(4):323-7. [4]. Preparation method of 2-naphthylamine 6,8 disulfonic acid. CN102295585A. Chemical & Physical Properties Density 0.881 g/mL at 25 °C(lit.) Boiling Point 159-161 °C(lit.) Melting Point −69 °C(lit.) Molecular Formula C10H8KNO6S2 Molecular Weight 341.40200 Flash Point 107 °F Exact Mass 340.94300 PSA 154.35000 LogP 3.31560 Index of Refraction n20/D 1.425(lit.) |
| Use of | 2-Naphthylamine-6,8-disulfonic acid potassium is chemical that can be used for preparing dyestuff, medicine, agricultural chemicals etc[1]. Properties Name 2-Naphthylamine-6,8-Disulfonic Acid Monopotassium Salt Synonym More Synonyms Biological Activity Description 2-Naphthylamine-6,8-disulfonic acid potassium is chemical that can be used for preparing dyestuff, medicine, agricultural chemicals etc[1]. Related Catalog Signaling Pathways >> Others >> Others Research Areas >> Inflammation/Immunology References [1]. G T Tan, et al. Potential anti-AIDS naphthalenesulfonic acid derivatives. Synthesis and inhibition of HIV-1 induced cytopathogenesis and HIV-1 and HIV-2 reverse transcriptase activities. J Med Chem. 1992 Dec 25;35(26):4846-53. [2]. K B Lee, et al. A new method for sequencing linear oligosaccharides on gels using charged, fluorescent conjugates. Carbohydr Res. 1991 Jul 18;214(1):155-68. [3]. Ningguo Gao, et al. Fluorophore-assisted carbohydrate electrophoresis: a sensitive and accurate method for the direct analysis of dolichol pyrophosphate-linked oligosaccharides in cell cultures and tissues. Methods. 2005 Apr;35(4):323-7. [4]. Preparation method of 2-naphthylamine 6,8 disulfonic acid. CN102295585A. Chemical & Physical Properties Molecular Formula C10H8KNO6S2 Exact Mass 340.94300 PSA 154.35000 LogP 3.31560 |
| Tax Rebate | 9.0% |
| Supervision | None. MFN tariff: 6.5%. Ordinary tariff: 30.0% |
| Transport Info | Product name: Purity: 98.0% |
| MSDS Transport Info | Module 14. Shipping information United Nations classification: inconsistent with United Nations classification standards UN number: not specified |
| Related Products in Specialty Chemicals | ||
|---|---|---|
| Rogaratinib | 1443530-05-9 | 2A-2197980 |
| Perfluoro-n-[1,2,3,4-13C4]-octanoic Acid | 960315-48-4 | 2A-1197959 |
| Sodium Heptadecafluorononanoate | 21049-39-8 | 2A-1197982 |
| Electrolytic Silver Catalyst | 2A-2197986 | 2A-2197986 |
| O-methyl acetate chlorobenzene | 2A-2197987 | 2A-2197987 |
| 3-(5-methyl-1H-tetrazol-1-yl)aniline | 500701-24-6 | 2A-1198005 |
| 2,6-BIS(4-AZIDOBENZYLIDENE)-4-METHYLCYCLOHEXANONE | 5284-79-7 | 2A-1198006 |
| N-Hydroxynaphthalimide triflate | 85342-62-7 | 2A-1198012 |
| 8-Nitro-2-tetrazol-5-yl-4-oxo-4H-1-benzopyran | 141283-42-3 | 2A-1198018 |
| (Z)-hexadec-11-en-1-ol | 56683-54-6 | 2A-1198019 |
| Browse all Specialty Chemicals products » | ||
Phone:
630-322-8886
630-322-8887
Email:
Office Locations:
Chicago, IL, USA
San Francisco, CA, USA
EN
SDS