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A propos de cet article
Formule linéaire :
H2NC10H5(OH)SO3H
Numéro CAS:
Poids moléculaire :
239.25
UNSPSC Code:
41116105
NACRES:
NA.21
PubChem Substance ID:
EC Number:
204-147-3
Beilstein/REAXYS Number:
2697469
MDL number:
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Service technique
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Laissez-nous vous aiderQuality Level
assay
≥90.0% (CHN)
form
powder
quality
for spectrophotometric det. of Si
technique(s)
UV/Vis spectroscopy: suitable
mp
290 °C (dec.) (lit.)
SMILES string
Nc1c(O)cc(c2ccccc12)S(O)(=O)=O
InChI
1S/C10H9NO4S/c11-10-7-4-2-1-3-6(7)9(5-8(10)12)16(13,14)15/h1-5,12H,11H2,(H,13,14,15)
InChI key
RXCMFQDTWCCLBL-UHFFFAOYSA-N
General description
4-Amino-3-hydroxy-1-naphthalenesulfonic acid is an aromatic amino-sulfonic acid.
Application
4-Amino-3-hydroxy-1-naphthalenesulfonic acid has been used to study separation of aromatic sulfonated compounds using Ion-interaction high-performance liquid chromatography and micellar electrokinetic capillary chromatography techniques. It has also been used as a starting material which when reacted with palmitoyl chloride yields the following derivatives:
- 2′-Pentadecylnaphth[3,4-d]oxazole-1-sulfonic acid
- 4-Amino-3-(palmitoyloxy)-1-naphthalenesufonic acid
- 4-(Palmitoylamino)-3-hydroxy-1-naphthalenesulfonic acid
- 4-(Palmitoylamino)-3-(palmitoyloxy)-1-naphthalenesulfonic acid
Other Notes
Reagent for the spectrophotometric det. of silicon
1 of 1
Cet article | |||
|---|---|---|---|
| technique(s) UV/Vis spectroscopy: suitable | technique(s) - | technique(s) - | technique(s) - |
| mp 290 °C (dec.) (lit.) | mp 290 °C (dec.) (lit.) | mp ≥300 °C (lit.) | mp - |
| form powder | form powder | form powder | form powder |
| Quality Level 100 | Quality Level 200 | Quality Level 200 | Quality Level 100 |
| quality for spectrophotometric det. of Si | quality - | quality - | quality - |
| assay ≥90.0% (CHN) | assay ≥90% | assay 97% | assay ≥90% (T) |
Classe de stockage
11 - Combustible Solids
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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Synthesis of naphthalenesulfonic acid small molecules as selective inhibitors of the DNA polymerase and ribonuclease H activities of HIV-1 reverse transcriptase.
Mohan P
Journal of Medicinal Chemistry, 37(16), 2513-2519 (1994)
F.A. Sorrentino et al.
Microchemical Journal, Devoted to the Application of Microtechniques in All Branches of Science, 15, 441-441 (1970)
Ion-interaction high-performance liquid chromatography and micellar electrokinetic capillary chromatography: two complementary techniques for the separation of aromatic sulfonated compounds.
Angelino, S., et al.
Journal of Chromatography A, 845.1, 257-271 (1999)
Numéro d'article de commerce international
| Référence | GTIN |
|---|---|
| W267708-5KG-K | 04061837806988 |
| 1A00900-25MG | 04065269096726 |
| 1A02470-25MG | 04065269107453 |
| 8212430250 | 04022536476605 |
| 59932-1ML | 04061832644738 |
| W267708-SAMPLE-K | 04061837515910 |
| W267708-1KG-K | 04061837806964 |
| W267708-25KG-K | 04061837806971 |
| W267708-10KG-K | 04061837806957 |
| 1A01390-25MG | 04065269107361 |
| 8212431000 | 04022536476612 |


