
CAS Number10139-02-3
Synonyms2-Nitrophenyl 2-acetamido-2-deoxyhexopyranoside; 4-Nitrophenyl N-acetyl-1-thio-|A-D-glucosaminide; MFCD00006592; p-Nitrophenyl 2-Acetamido-2-deoxy-Alpha-D-glucopyranoside; EINECS 233-392-9; p-nitrophenyllacto-N-biose; p-Nitrophenyl 2-acetamido-2-deoxy-1-thio-|A-D-glucopyranoside
Molecular FormulaC14H18N2O8
Molecular Weight342.30
Purity≥98%
Density1.5±0.1 g/cm3
Boiling Point685.2±55.0 °C at 760 mmHg
Melting Point264ºC
Appearancepowder
EINECS233-392-9
| Chemical & Physical Properties | |
|---|---|
| CAS Number | 10139-02-3 |
| Catalog No. | 2A-0160366 |
| Chinese Name | 4-硝基苯-N-乙酰基-Alpha-D-氨基葡糖苷 |
| Synonyms | 2-Nitrophenyl 2-acetamido-2-deoxyhexopyranoside; 4-Nitrophenyl N-acetyl-1-thio-|A-D-glucosaminide; MFCD00006592; p-Nitrophenyl 2-Acetamido-2-deoxy-Alpha-D-glucopyranoside; EINECS 233-392-9; p-nitrophenyllacto-N-biose; p-Nitrophenyl 2-acetamido-2-deoxy-1-thio-|A-D-glucopyranoside |
| Molecular Formula | C14H18N2O8 |
| Molecular Weight | 342.30 |
| Purity | ≥98 |
| Density | 1.5±0.1 g/cm3 |
| Boiling Point | 685.2±55.0 °C at 760 mmHg |
| Melting Point | 264ºC |
| Appearance | powder |
| Storage Condition | Store in an airtight container. Store in dry area. |
| Application | 4-Nitrophenyl N-acetyl-α-D-glucosamine is a 4-nitrophenyl conjugated substrate used to determine enzyme specificity [1]. |
| EINECS | 233-392-9 |
| HTC | 0 |
| UN(IATA) | 0 |
| PubChem ID | 24897691 |
| MDL Number | MFCD00006592 |
| SMILES | CC(=O)N[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@@H]1Oc2ccc(cc2)[N+]([O-])=O |
| InChI | 1S/C14H18N2O8/c1-7(18)15-11-13(20)12(19)10(6-17)24-14(11)23-9-4-2-8(3-5-9)16(21)22/h2-5,10-14,17,19-20H,6H2,1H3,(H,15,18)/t10-,11-,12-,13-,14+/m1/s1 |
| InChI Key | OMRLTNCLYHKQCK-KSTCHIGDSA-N |
| NACRES Code | NA.32 |
| UNSPSC | 12352204 |
| MSDS | msds/160366_1_10139_02_3.pdf |
| Bioactivity | 4-Nitrophenyl N-acetyl-α-D-glucosaminide is a 4-nitrophenyl- conjugated substrate for determining the enzymatic specificity[1]. Related Catalog Research Areas >> Others Signaling Pathways >> Others >> Others References [1]. Daniel Garrido, et al. Release and utilization of N-acetyl-D-glucosamine from human milk oligosaccharides by Bifidobacterium longum subsp. Infantis. Anaerobe. 2012 Aug;18(4):430-5. Chemical & Physical Properties Density 1.5±0.1 g/cm3 Boiling Point 685.2±55.0 °C at 760 mmHg Melting Point 264ºC Molecular Formula C14H18N2O8 Molecular Weight 342.301 Flash Point 368.2±31.5 °C Exact Mass 342.106323 PSA 154.07000 LogP -0.30 Vapour Pressure 0.0±2.2 mmHg at 25°C Index of Refraction 1.620 InChIKey OMRLTNCLYHKQCK-KSTCHIGDSA-N SMILES CC(=O)NC1C(Oc2ccc([N+](=O)[O-])cc2)OC(CO)C(O)C1O Storage condition −20°C |
| Use of | 4-Nitrophenyl N-acetyl-α-D-glucosaminide is a 4-nitrophenyl- conjugated substrate for determining the enzymatic specificity[1]. Properties Articles21 Name P-NITROPHENYL 2-ACETAMIDO-2-DEOXY-α-D-GLUCOPYRANOSIDE Synonym More Synonyms Biological Activity Description 4-Nitrophenyl N-acetyl-α-D-glucosaminide is a 4-nitrophenyl- conjugated substrate for determining the enzymatic specificity[1]. Related Catalog Research Areas >> Others Signaling Pathways >> Others >> Others References [1]. Daniel Garrido, et al. Release and utilization of N-acetyl-D-glucosamine from human milk oligosaccharides by Bifidobacterium longum subsp. Infantis. Anaerobe. 2012 Aug;18(4):430-5. Chemical & Physical Properties Molecular Formula C14H18N2O8 Exact Mass 342.106323 PSA 154.07000 LogP -0.30 Index of Refraction 1.620 InChIKey OMRLTNCLYHKQCK-KSTCHIGDSA-N |
| Transport Info | Product name: 4-nitrophenyl N-acetyl-α-D-glucosamine |
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