| Chemical & Physical Properties | |
|---|---|
| CAS Number | 1223-07-0 |
| Catalog No. | 2A-9026524 |
| Chinese Name | 4-硝基苯基α- L -阿拉伯吡喃果糖苷 |
| Synonyms | (2S,3R,4S,5S)-2-(4-nitrophenoxy)tetrahydro-2H-pyran-3,4,5-triol |
| Molecular Formula | C11H13NO7 |
| Molecular Weight | 271.22 |
| Purity | ≥98 (HPLC) |
| Density | 1.597g/cm3 |
| Boiling Point | 523.2ºC at 760mmHg |
| Melting Point | 205ºC |
| Appearance | powder |
| Storage Condition | −20°C |
| Application | p-Nitrophenyl α-L-arabinopyranoside is a biochemical reagent. p-Nitrophenyl α-L-arabinopyranoside can be hydrolyzed by recombinant BgaA (rBgaA, isolated from E. coli BL21 (DE3) strain harboring pEBGA2 |
| PubChem ID | 24897649 |
| MDL Number | MFCD00151486 |
| SMILES | OC1COC(Oc2ccc(cc2)N(=O)=O)C(O)C1O |
| InChI | 1S/C11H13NO7/c13-8-5-18-11(10(15)9(8)14)19-7-3-1-6(2-4-7)12(16)17/h1-4,8-11,13-15H,5H2 |
| InChI Key | MLJYKRYCCUGBBV-UHFFFAOYSA-N |
| NACRES Code | NA.32 |
| UNSPSC | 12352204 |
| Hazard Symbols | transportation |
| MSDS | msds/26524_1_1223_07_0.pdf |
| Bioactivity | p-Nitrophenyl α-L-arabinopyranoside is a biochemical reagent. p-Nitrophenyl α-L-arabinopyranoside can be hydrolyzed by recombinant BgaA (rBgaA, isolated from E. coli BL21 (DE3) strain harboring pEBGA29). p-Nitrophenyl α-L-arabinopyranoside has potential application in enzyme activity detection[1][3]. Related Catalog Research Areas >> Others In Vitro p-Nitrophenyl α-L-arabinopyranoside has an affinity Km value of 6.06 mM for rBgaA[1]. p-Nitrophenyl α-L-arabinopyranoside has high activity against the xylosidase-arabinosidase (xarB) gene [2]. Application of p-Nitrophenyl α-L-arabinopyranoside in enzyme activity detection [3] (1) 200 µL 2 mM p-Nitrophenyl α-L-arabinopyranoside, 100 µL enzyme, 300 µL 50 mM phosphate buffer (pH 7.0), incubated at 37°C for 0.5, 1 and 5 h. (2) Add 400 µL 0.5 M sodium hydroxide to stop the reaction. (3) Measure the absorbance of the mixture at 405 nm. Note: In the presence of ginsenosides, use butanol extraction to terminate the reaction. References [1]. Kosugi A, et al. Characterization of two noncellulosomal subunits, ArfA and BgaA, from Clostridium cellulovorans that cooperate with the cellulosome in plant cell wall degradation. J Bacteriol. 2002 Dec;184(24):6859-65. [2]. Mai V, et al. Cloning, sequencing, and characterization of the bifunctional xylosidase-arabinosidase from the anaerobic thermophile thermoanaerobacter ethanolicus. Gene. 2000 Apr 18;247(1-2):137-43. [3]. Shin H Y, et al. Purification and Characterization ofα-l-Arabinopyranosidase andα-l-Arabinofuranosidase from Bifidobacterium breve K-110, a Human Intestinal Anaerobic Bacterium Metabolizing Ginsenoside Rb2 and Rc[J]. Applied and environmental microbiology, 2003, 69(12): 7116-7123. Chemical & Physical Properties Density 1.597g/cm3 Boiling Point 523.2ºC at 760mmHg Melting Point 205ºC Molecular Formula C11H13NO7 Molecular Weight 271.22300 Flash Point 270.2ºC Exact Mass 271.06900 PSA 124.97000 Vapor Pressure 8.94E-12mmHg at 25°C Index of Refraction 1.654 InChIKey MLJYKRYCCUGBBV-MMWGEVLESA-N SMILES O=[N+]([O-])c1ccc(OC2OCC(O)C(O)C2O)cc1 Storage condition −20°C |
| Use of | p-Nitrophenyl α-L-arabinopyranoside is a biochemical reagent. p-Nitrophenyl α-L-arabinopyranoside can be hydrolyzed by recombinant BgaA (rBgaA, isolated from E. coli BL21 (DE3) strain harboring pEBGA29). p-Nitrophenyl α-L-arabinopyranoside has potential application in enzyme activity detection[1][3]. Properties Name (2S,3R,4S,5S)-2-(4-nitrophenoxy)oxane-3,4,5-triol Synonym More Synonyms p-nitrophenyl alpha-l-arabinopyranoside Biological Activity Description p-Nitrophenyl α-L-arabinopyranoside is a biochemical reagent. p-Nitrophenyl α-L-arabinopyranoside can be hydrolyzed by recombinant BgaA (rBgaA, isolated from E. coli BL21 (DE3) strain harboring pEBGA29). p-Nitrophenyl α-L-arabinopyranoside has potential application in enzyme activity detection[1][3]. Related Catalog Research Areas >> Others References [1]. Kosugi A, et al. Characterization of two noncellulosomal subunits, ArfA and BgaA, from Clostridium cellulovorans that cooperate with the cellulosome in plant cell wall degradation. J Bacteriol. 2002 Dec;184(24):6859-65. [2]. Mai V, et al. Cloning, sequencing, and characterization of the bifunctional xylosidase-arabinosidase from the anaerobic thermophile thermoanaerobacter ethanolicus. Gene. 2000 Apr 18;247(1-2):137-43. [3]. Shin H Y, et al. Purification and Characterization ofα-l-Arabinopyranosidase andα-l-Arabinofuranosidase from Bifidobacterium breve K-110, a Human Intestinal Anaerobic Bacterium Metabolizing Ginsenoside Rb2 and Rc[J]. Applied and environmental microbiology, 2003, 69(12): 7116-7123. Chemical & Physical Properties Molecular Formula C11H13NO7 Exact Mass 271.06900 PSA 124.97000 Index of Refraction 1.654 InChIKey MLJYKRYCCUGBBV-MMWGEVLESA-N |
| Transport Info | Product name: Purity: 98.0% |
| MSDS Transport Info | Module 14. Shipping information 14.1 UN dangerous goods number European Land Transport Dangerous Regulations: -International Maritime Dangerous Regulations: -International Air Transport Dangerous Regulations: - 14.2 Names specified by the United Nations (UN) European Land Transport Dangerous Regulations: Non-dangerous goods IMDG Code: Non-dangerous goods International air transport dangerous goods regulations: non-dangerous goods 14.3 Transport hazard categories European Land Transport Dangerous Regulations: -International Maritime Dangerous Regulations: -International Air Transport Dangerous Regulations: - 14.4 Package group European Land Transport Dangerous Regulations: -International Maritime Dangerous Regulations: -International Air Transport Dangerous Regulations: - 14.5 Environmental hazards European Land Transport Dangerous Regulations: No International Maritime Transport Dangerous Regulations Maritime Pollutants: No International Air Transport Risk Regulations: No 14.6 Special reminder to users No data available |
| Related Products in Specialty Chemicals | ||
|---|---|---|
| 1,3-Dicyclohexylthiourea | 1212-29-9 | 2A-9026511 |
| 4-Chloro-N-(pyridin-2-yl)benzenesulfonamide | 1213-38-3 | 2A-9026512 |
| 2-(2-Hydroxyphenyl)-4H-benzo[e][1,3]oxazin-4-one | 1218-69-5 | 2A-9026520 |
| Octyl paraben | 1219-38-1 | 2A-9026521 |
| 2,2-Bis(3-amino-4-hydroxyphenyl)propane | 1220-78-6 | 2A-9026522 |
| Bis(4-aminophenoxy)dimethylsilane | 1223-16-1 | 2A-9026525 |
| 4,4'-Bis(dimethylamino)thiobenzophenone | 1226-46-6 | 2A-0202268 |
| 3-Nitrophenyl sulphone | 1228-53-1 | 2A-9026527 |
| (+)-Dehydroabietic acid | 1231-75-0 | 2A-9026531 |
| Biperiden hydrochloride | 1235-82-1 | 2A-9026534 |
| Browse all Specialty Chemicals products » | ||
Phone:
630-322-8886
630-322-8887
Email:
Office Locations:
Chicago, IL, USA
San Francisco, CA, USA
EN
SDS