
CAS Number103404-75-7
SynonymsD-Luciferin sodium salt, 99%; 4-Thiazolecarboxylic acid, 4,5-dihydro-2-(6-hydroxy-2-benzothiazolyl)-, sodium salt, (4S)- (1:1); Sodium (4S)-2-(6-hydroxy-1,3-benzothiazol-2-yl)-4,5-dihydro-1,3-thiazole-4-carboxylate; MFCD00044938; D-Luciferinsodiumsaltmonohydrate; Sodium (S)-2-(6-hydroxybenzo[d]thiazol-2-yl)-4,5-dihydrothiazole-4-carboxylate; D-LUCIFERIN SODIUM SALT; D-Luciferin (sodium salt)
Molecular FormulaC11H7N2NaO3S2
Molecular Weight302.30
Purity≥98 (HPLC)%
Boiling Point473.7ºC at 760mmHg
Appearancelyophilized powder
Symbol
Signal WordWarning
| Chemical & Physical Properties | |
|---|---|
| CAS Number | 103404-75-7 |
| Catalog No. | 2A-9049996 |
| Chinese Name | D-荧光素钠盐 |
| Synonyms | D-Luciferin sodium salt, 99%; 4-Thiazolecarboxylic acid, 4,5-dihydro-2-(6-hydroxy-2-benzothiazolyl)-, sodium salt, (4S)- (1:1); Sodium (4S)-2-(6-hydroxy-1,3-benzothiazol-2-yl)-4,5-dihydro-1,3-thiazole-4-carboxylate; MFCD00044938; D-Luciferinsodiumsaltmonohydrate; Sodium (S)-2-(6-hydroxybenzo[d]thiazol-2-yl)-4,5-dihydrothiazole-4-carboxylate; D-LUCIFERIN SODIUM SALT; D-Luciferin (sodium salt) |
| Molecular Formula | C11H7N2NaO3S2 |
| Molecular Weight | 302.30 |
| Purity | ≥98 (HPLC) |
| Boiling Point | 473.7ºC at 760mmHg |
| Appearance | lyophilized powder |
| Water Solubility | H2O: soluble |
| Storage Condition | Store airtight in a cool, dry warehouse. Refrigera |
| Application | D-Luciferin sodium salt is a substrate for luciferase, which can catalyze bioluminescent insects to produce typical yellow-green light. |
| HTC | 2934999090 |
| PubChem ID | 24896446 |
| MDL Number | MFCD00044938 |
| SMILES | [Na+].Oc1ccc2nc(sc2c1)C3=N[C@H](CS3)C([O-])=O |
| InChI | 1S/C11H8N2O3S2.Na/c14-5-1-2-6-8(3-5)18-10(12-6)9-13-7(4-17-9)11(15)16;/h1-3,7,14H,4H2,(H,15,16);/q;+1/p-1/t7-;/m1./s1 |
| InChI Key | LILQLBIQROYWIA-OGFXRTJISA-M |
| NACRES Code | NA.32 |
| UNSPSC | 12352204 |
| Hazard Symbols | transportation |
| MSDS | msds/49996_1_103404_75_7.pdf |
| Bioactivity | D-Luciferin sodium salt is the substrate of luciferases that catalyze the production of light in bioluminescent insects. Related Catalog Signaling Pathways >> Others >> Others Dye Reagents Research Areas >> Others In Vitro D-luciferin is the natural substrate of the enzyme luciferase (Luc), that catalyzes the production of the typical yellowgreen light of fireflies.The present review covers the synthesis of D-luciferin and derivatives or analogues that are substrates or inhibitors of the luciferase from the American firefly Photinus pyralis, the enzyme more frequently used in techniques of in vitro and optical imaging[1]. In Vivo Bioluminescence imaging (BLI) using the firefly luciferase (Fluc) as a reporter gene and D-luciferin as a substrate is currently the most widely employed technique. The total signal intensity is plotted against the time after D-luciferin injection to generate a time-intensity curve. In addition to the peak signal, the signals at fixed time points (5, 10, 15, and 20 min) after D-luciferin injection are determined as alternatives to the peak signal. The signal in a given time-intensity curve is normalized for the peak signal in the curve to represent the pattern of temporal changes after D-luciferin injection[2]. Animal Admin Mice[2] In vivo BLI is performed using a cooled charge-coupled device camera system (IVIS Imaging System 100) 3, 5, 7, 10, 12, 14, 19, 21, 24, and 28 days after the inoculation of HCT116-Luc cells. Mice are injected with 75 mg/kg D-luciferin in 100 L of phosphate-buffered saline subcutaneously near the scapula and were placed in the light-tight chamber of the imaging system under isoflurane anesthesia. Beginning 5 min after injection, dorsal luminescent images with an exposure time of 1 s are acquired sequentially at a rate of one image per min until 20 min after D-luciferin injection. Data acquisition is continued until 40 min postinjection on days 3 or 5 and until 25 min on day 7, because of the prolonged time course of light emission. Binning is 4 and the field of view is 15 cm. References [1]. Giuseppe Meroni, et al. D-Luciferin, derivatives and analogues: synthesis and in vitro/in vivo luciferase-catalyzed bioluminescent activity. ARKIVOC 2009 (i) 265-288. [2]. Inoue Y, et al. Timing of imaging after d-luciferin injection affects the longitudinal assessment of tumor growthusing in vivo bioluminescence imaging. Int J Biomed Imaging. 2010;2010:471408. Chemical & Physical Properties Boiling Point 473.7ºC at 760mmHg Molecular Formula C11H7N2NaO3S2 Molecular Weight 302.305 Flash Point 240.3ºC Exact Mass 301.979584 PSA 139.15000 LogP 0.04940 Vapour Pressure 2.78E-10mmHg at 25°C InChIKey LILQLBIQROYWIA-OGFXRTJISA-M SMILES O=C([O-])C1CSC(c2nc3ccc(O)cc3s2)=N1.[Na+] Storage condition −20°C Water Solubility H2O: soluble |
| Use of | D-Luciferin sodium salt is the substrate of luciferases that catalyze the production of light in bioluminescent insects. Properties Name D-Luciferin sodium salt monohydrate Synonym More Synonyms D-Luciferin (sodium salt) Biological Activity Description D-Luciferin sodium salt is the substrate of luciferases that catalyze the production of light in bioluminescent insects. Related Catalog Signaling Pathways >> Others >> Others Dye Reagents Research Areas >> Others In Vitro D-luciferin is the natural substrate of the enzyme luciferase (Luc), that catalyzes the production of the typical yellowgreen light of fireflies.The present review covers the synthesis of D-luciferin and derivatives or analogues that are substrates or inhibitors of the luciferase from the American firefly Photinus pyralis, the enzyme more frequently used in techniques of in vitro and optical imaging[1]. References [1]. Giuseppe Meroni, et al. D-Luciferin, derivatives and analogues: synthesis and in vitro/in vivo luciferase-catalyzed bioluminescent activity. ARKIVOC 2009 (i) 265-288. [2]. Inoue Y, et al. Timing of imaging after d-luciferin injection affects the longitudinal assessment of tumor growthusing in vivo bioluminescence imaging. Int J Biomed Imaging. 2010;2010:471408. Chemical & Physical Properties Molecular Formula C11H7N2NaO3S2 Exact Mass 301.979584 PSA 139.15000 LogP 0.04940 InChIKey LILQLBIQROYWIA-OGFXRTJISA-M Water Solubility H2O: soluble |
| Tax Rebate | 13.0% |
| Supervision | None. MFN tariff: 6.5%. Ordinary tariff: 20.0% |
| Transport Info | Shipping Name: UN |
| 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 United Nations shipping name 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 Danger Regulations: No International Maritime Danger Regulations International Air Transport Danger Regulations: No Marine pollutants (yes/no): No 14.6 Special reminder to users No data available |
| Related Products in Biotechnology & Diagnostics | ||
|---|---|---|
| Cytidine 5'-diphosphoglycerol disodium salt | 102601-56-9 | 2A-9049919 |
| 2-Cyanoethyl N,N,N',N'-tetraisopropylphosphorodiamidite | 102691-36-1 | 2A-9049926 |
| 2'-Deoxycytidine-5'-triphosphoric acid disodium salt | 102783-51-7 | 2A-9049932 |
| 2'-Deoxyguanosine-5'-diphosphate trisodium salt | 102783-74-4 | 2A-9049935 |
| 2'-Deoxyuridine-5'-triphosphate trisodium salt | 102814-08-4 | 2A-9049937 |
| Fmoc-N-methyl-D-valine | 103478-58-6 | 2A-9050005 |
| Fmoc-N-methyl-D-leucine | 103478-63-3 | 2A-9050007 |
| Fmoc-D-glutamic acid gamma-tert-butyl ester | 104091-08-9 | 2A-9050078 |
| Boc-L-4-benzoylphenylalanine | 104504-43-0 | 2A-9050116 |
| PEG-40 SORBITAN LANOLATE | 8036-77-9 | 2A-9050138 |
| Browse all Biotechnology & Diagnostics products » | ||
Phone:
630-322-8886
630-322-8887
Email:
Office Locations:
Chicago, IL, USA
San Francisco, CA, USA