Cell Culture Supplements & Reagents
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Arabinofuranose SMB00918-25MG
Empirical Formula (Hill Notation): C5H10O5 Molecular Weight: 150.13 MDL number: MFCD30066138 General descriptionArabinofuranose refers to the furanose form of arabinose, which is an optical isomer of arabinose. L-Arabinose is more common than D-Arabinose in nature as a component of biopolymers such as hemicellulose and pectin. (1),ApplicationMetabolomics researchПараметрыassay ≥95% (HPLC) form powder color off-white storage temp. 2-8°C InChI key HMFHBZSHGGEWLO-HWQSCIPKSA-N
Safety InformationWGK Germany WGK 3 Flash Point F Not applicable Flash Point C Not applicable Узнать цену -
Arbutin
Empirical Formula (Hill Notation): C12H16O7 CAS Number: 497-76-7 Molecular Weight: 272.25 Beilstein/REAXYS Number: 89673 EC Number: 207-850-3 MDL number: MFCD00016915 PubChem Substance ID: 24890841 NACRES: NA.25
Кат. номер A4256-10G A4256-50G A4256-25G ApplicationArbutin, a glycosylated hydroquinone, is used in studies on melanin biosynthesis and as an inhibitor to identify, differentiate and characterize tyrosinase(s).Biochem/physiol ActionsArbutin is a glycosylated hydroquinone used in traditional Chinese medicine (TCM). Arbutin inhibits melanin formation due to its tyrosinase inhibitory activity.Other NotesTandem Mass Spectrometry data independently generated by Scripps Center for Metabolomics is available to view or download in PDF. A4256.pdf , Tested metabolites are featured on Scripps Center for Metabolomics METLIN Metabolite Database. To learn more, visit sigma.com/metlin.,ПараметрыQuality Level 200, biological source synthetic or plant assay ≥98% form powder optical activity [α]25/D -66.0 to -62.0 °, c = 3% (w/v) in water application(s) HPLC: suitable mp 195 °C SMILES string OC[C@H]1O[C@@H](Oc2ccc(O)cc2)[C@H](O)[C@@H](O)[C@@H]1O InChI 1S/C12H16O7/c13-5-8-9(15)10(16)11(17)12(19-8)18-7-3-1-6(14)2-4-7/h1-4,8-17H,5H2/t8-,9-,10+,11-,12-/m1/s1 InChI key BJRNKVDFDLYUGJ-RMPHRYRLSA-N
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Astragaloside II
Empirical Formula (Hill Notation): C43H70O15 CAS Number: 84676-89-1 Molecular Weight: 827.01 MDL number: MFCD12546127 PubChem Substance ID: 329824948 NACRES: NA.25
Кат. номер SMB00316-5MG SMB00316-10MG General descriptionAstragaloside II is a saponin found in the root of Astragalus propinquus, which is known as hung q in Traditional Chinese Medicine.Packaging5 mg in glass bottleBiochem/physiol ActionsAstragaloside II stimulates osteoblast differentiation resulting in bone formation.ПараметрыQuality Level 200, biological source plant (Astragalus membranaceus) assay 92% (HPLC) form powder storage temp. 20°C SMILES string CC1(C)[C@@H](O[C@]2([H])OC[C@@H](O)[C@H](O)[C@H]2OC(C)=O)CC[C@@]3(C4)[C@@]1([H])[C@@H](O[C@]5([H])O[C@H](CO)[C@@H](O)[C@H](O)[C@H]5O)C[C@]6([H])[C@@]34CC[C@]7(C)[C@]([C@]8(C)O[C@H](C(O)(C)C)CC8)([H])[C@@H](O)C[C@@]67C InChI 1S/C43H70O15/c1-20(45)54-32-28(48)22(47)18-53-36(32)57-26-10-12-43-19-42(43)14-13-39(6)33(41(8)11-9-27(58-41)38(4,5)52)21(46)16-40(39,7)25(42)15-23(34(43)37(26,2)3)55-35-31(51)30(50)29(49)24(17-44)56-35/h21-36,44,46-52H,9-19H2,1-8H3/t21-,22+,23-,24+,25-,26-,27-,28-,29+,30-,31+,32+,33-,34-,35+,36-,39+,40-,41+,42-,43+/m0/s1 InChI key AYWNHWGQTMCQIV-PENCHUSISA-N
Safety InformationRIDADR NONH for all modes of transport WGK Germany WGK 3 Flash Point F Not applicable Flash Point C Not applicable Узнать цену -
Astragaloside III
Empirical Formula (Hill Notation): C41H68O14 CAS Number: 84687-42-3 Molecular Weight: 784.97 PubChem Substance ID: 329824949 NACRES: NA.25
Кат. номер SMB00317-5MG SMB00317-10MG General descriptionAstragaloside III is a saponin found in the root of Astragalus propinquus, which is known as hung q in Traditional Chinese Medicine.Packaging5 mg in glass bottleПараметрыQuality Level 200, biological source plant (Astragalus membranaceus) assay 96% (HPLC) form powder storage temp. 20°C SMILES string CC(O)(C)[C@H](CC1)C[C@@]1(C)[C@]2([H])[C@@]3(C)CC[C@]45[C@@]([C@]3(C)C[C@@H]2O)([H])C[C@H](O)C6C(C)(C)[C@@H](O[C@@]7([H])[C@H](O[C@]8([H])O[C@H](CO)[C@@H](O)[C@H](O)[C@H]8O)[C@@H](O)[C@H](O)CO7)CC[C@@]64C5 InChI 1S/C42H70O13/c1-36(2)26(54-35-31(27(47)23(46)18-52-35)55-34-30(50)29(49)28(48)24(17-43)53-34)9-11-42-19-41(42)13-12-39(6)33(38(5)10-8-20(15-38)37(3,4)51)22(45)16-40(39,7)25(41)14-21(44)32(36)42/h20-35,43-51H,8-19H2,1-7H3/t20-,21+,22+,23-,24-,25+,26+,27+,28-,29+,30-,31-,32?,33-,34+,35+,38+,39-,40+,41+,42-/m1/s1 InChI key UBLUIAORQHLKTI-YMVJACEHSA-N
Safety InformationRIDADR NONH for all modes of transport WGK Germany WGK 3 Flash Point F Not applicable Flash Point C Not applicable Узнать цену -
Benzyl 2-acetamido-2-deoxy--D-galactopyranoside
Empirical Formula (Hill Notation): C15H21NO6 CAS Number: 3554-93-6 Molecular Weight: 311.33 MDL number: MFCD00057920 PubChem Substance ID: 24891802 NACRES: NA.25
Кат. номер B4894-100MG B4894-500MG B4894-25MG Packaging100, 500 mg in poly bottle
25 mg in glass insertBiochem/physiol ActionsBenzyl-N-acetyl--galactosaminide inhibits glycosyltransferase incorporation of glucosamine into O-glycans. Suppresses mucin biosynthesis and inhibits MUC1 expression in breast cancer cell line MDF-7.ПараметрыQuality Level 100, assay 97% (TLC) form powder mp 204-208 °C solubility methanol: soluble 10 mg/mL, clear storage temp. 20°C SMILES string CC(=O)NC1C(O)C(O)C(CO)OC1OCc2ccccc2 InChI 1S/C15H21NO6/c1-9(18)16-12-14(20)13(19)11(7-17)22-15(12)21-8-10-5-3-2-4-6-10/h2-6,11-15,17,19-20H,7-8H2,1H3,(H,16,18) InChI key SKOZFDIGKDPQBO-UHFFFAOYSA-N
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Benzyl 2-acetamido-2-deoxy-3-O--D-galactopyranosyl--D-galactopyranoside
Empirical Formula (Hill Notation): C21H31NO11 CAS Number: 3554-96-9 Molecular Weight: 473.47 MDL number: MFCD00057916 PubChem Substance ID: 24891804 NACRES: NA.25
Кат. номер B5019-10MG B5019-5MG B5019-1MG ApplicationBenzyl 2-acetamido-2-deoxy-3-O-β-D-galactopyranosyl-α-D-galactopyranoside, a benzyl derivative of 2-acetamido-2-deoxy-3-O-β-D-galactopyranosyl-α-D-galactopyranoside, may be used in structural studies on the Lewis lec antigen.Packaging5 mg in glass bottle
10 mg in poly bottleПараметрыQuality Level 200, assay 97% (TLC) form powder storage temp. 20°C SMILES string CC(=O)NC1C(OCc2ccccc2)OC(CO)C(O)C1OC3OC(CO)C(O)C(O)C3O InChI 1S/C21H31NO11/c1-10(25)22-14-19(33-21-18(29)17(28)15(26)12(7-23)32-21)16(27)13(8-24)31-20(14)30-9-11-5-3-2-4-6-11/h2-6,12-21,23-24,26-29H,7-9H2,1H3,(H,22,25) InChI key MYDRTQFLXCNCAG-UHFFFAOYSA-N
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Biotin--D-glucopyranoside polyacrylamide
MDL number: MFCD03456207 NACRES: NA.25
Кат. номер B8807-1MG B8807-1MG-PW ApplicationBiotin-β-D-glucopyranoside polyacrylamide may be used in the development of load-bearing hydrogels for tissue engineering applications.ПараметрыQuality Level 200, mol wt ~30 kDa storage temp. 2-8°C
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Biotin-dextran
MDL number: MFCD00130657 eCl@ss: 34058011 NACRES: NA.25
Кат. номер B9139-25MG B9139-10MG ApplicationBiotin-dextran is used in tissue staining to prepare neurons for detection by avidin-conjugated detection systems. It is taken up by neuronal processes and transported bi-directionally. It infiltrates axon boutons in the anterograde direction and dendritic processes in the retrograde direction. Staining can be observed in fixed and sectioned tissue from two days to two weeks after biotin-dextran is injected into the brain or spinal cord. It can also be applied to cut nerve tracts. Biotinylated neurons are detected by either light or electron microscopy following incubation with avidin-horseradish peroxidase conjugate and the electron-dense substrate 3,3′-diaminobenzidine (DAB).Packaging10, 25 mg in poly bottleПараметрыQuality Level 200, form powder mol wt 10,000 extent of labeling ~2 mol per mol solubility H2O: soluble 50 mg/mL, clear, colorless to faintly yellow conjugate biotin conjugate storage temp. 2-8°C
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Biotin-poly(ethyleneglycol)amine B9931-10MG
MDL number: MFCD03456227 NACRES: NA.25 ApplicationBiotin-poly(ethyleneglycol)amine may be used as a crosslink horse radish peroxide (HRP) enzyme to the surface of silver island films (SIFs). 1 Biotin PEG amine may be used to functionalize the surface of poly(lactic-co-glycolic acid) (PLGA) nanoparticles.
Biotin-poly(ethyleneglycol)amine (BPEG) is used to functionalize (biotin pegylate) surfaces of structures such as hydrogels, microspheres, quantum dots and nanoparticles to take advantage of biotin-avidin based targeting.Packaging10 mg in serum bottleПараметрыQuality Level 200, assay >90% form waxy solid mol wt average mol wt 720 Da loss <7% loss on drying conjugate biotin conjugate storage temp. 2-8°C
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Blue Dextran 90475-1G
CAS Number: 87915-38-6 MDL number: MFCD00130661 NACRES: NA.32 ПараметрыQuality Level 100, biological source synthetic form powder mol wt average mol wt 10,000 loss ≤10% loss on drying capacity 0.01-0.08 mmol/g loading storage temp. −20°C
Safety InformationRIDADR NONH for all modes of transport WGK Germany WGK 3 Flash Point F Not applicable Flash Point C Not applicable Узнать цену -
Blue Dextran 90008-1G
CAS Number: 87915-38-6 MDL number: MFCD00130661 NACRES: NA.32 ПараметрыQuality Level 100, biological source synthetic form powder mol wt average mol wt 5,000 loss ≤10% loss on drying capacity 0.01-0.08 mmol/g loading storage temp. −20°C
Safety InformationRIDADR NONH for all modes of transport WGK Germany WGK 3 Flash Point F Not applicable Flash Point C Not applicable Узнать цену -
Calcium -D-heptagluconate dihydrate
Empirical Formula (Hill Notation): C14H26CaO16 · 2H2O CAS Number: 10030-53-2 Molecular Weight: 526.46 Beilstein/REAXYS Number: 6104529 EC Number: 249-383-8 MDL number: MFCD00150972 PubChem Substance ID: 57647908 NACRES: NA.22
Кат. номер 21160-250G-F 21160-50G-F 21160-1KG-F ПараметрыQuality Level 100, assay 98.0% loss 8% loss on drying SMILES string [H]O[H].[H]O[H].OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)[C@@H](O)C(=O)O[Ca]OC(=O)[C@H](O)[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO InChI 1S/2C7H14O8.Ca.2H2O/c2*8-1-2(9)3(10)4(11)5(12)6(13)7(14)15;;;/h2*2-6,8-13H,1H2,(H,14,15);;2*1H2/q;;+2;;/p-2/t2*2-,3-,4+,5-,6-;;;/m11.../s1 InChI key JBMIEBJMNFOKBC-JRLDONDGSA-L
Safety InformationRIDADR NONH for all modes of transport WGK Germany WGK 3 Flash Point F Not applicable Flash Point C Not applicable Узнать цену -
Calcium -D-heptagluconate hydrate
Empirical Formula (Hill Notation): C14H26CaO16 · xH2O CAS Number: 17140-60-2 Molecular Weight: 490.42 (anhydrous basis) Beilstein/REAXYS Number: 6104529 EC Number: 241-203-6 MDL number: MFCD00150972 PubChem Substance ID: 57647907 NACRES: NA.22
Кат. номер 21155-250G-F 21155-1KG-F ПараметрыQuality Level 100, assay 98.0% (calc. based on dry substance) optical activity []20/D +2±0.2°, c = 5% in H2O loss ~5% loss on drying SMILES string O.O.OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)[C@@H](O)C(=O)O[Ca]OC(=O)[C@H](O)[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO InChI 1S/2C7H14O8.Ca.2H2O/c2*8-1-2(9)3(10)4(11)5(12)6(13)7(14)15;;;/h2*2-6,8-13H,1H2,(H,14,15);;2*1H2/q;;+2;;/p-2/t2*2-,3-,4+,5-,6-;;;/m11.../s1 InChI key JBMIEBJMNFOKBC-JRLDONDGSA-L
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Calcium D-gluconate
Empirical Formula (Hill Notation): C12H22CaO14 CAS Number: 299-28-5 Molecular Weight: 430.37 EC Number: 206-075-8 MDL number: MFCD00064209 PubChem Substance ID: 24893034
Кат. номер C8231-VAR C8231-1KG C8231-500G C8231-100G Параметрыbiological source synthetic (organic) Quality Level 200, grade anhydrous Agency/Method USP/NF, meets USP testing specifications (Not intended for use in preparing injectable dosage forms.) form powder Featured Industry Pharmaceutical (small molecule) SMILES string OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C(=O)O[Ca]OC(=O)[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO InChI 1S/2C6H12O7.Ca/c2*7-1-2(8)3(9)4(10)5(11)6(12)13;/h2*2-5,7-11H,1H2,(H,12,13);/q;;+2/p-2/t2*2-,3-,4+,5-;/m11./s1 InChI key NEEHYRZPVYRGPP-IYEMJOQQSA-L
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Calcium D-gluconate monohydrate
Empirical Formula (Hill Notation): C12H22CaO14 · H2O CAS Number: 66905-23-5 Molecular Weight: 448.39 Beilstein/REAXYS Number: 3919646 MDL number: MFCD00150787 PubChem Substance ID: 24895178 NACRES: NA.21
Кат. номер G4625-500G G4625-1KG G4625-100G Параметрыbiological source synthetic (organic) Quality Level 200, assay 98% form powder application(s) HPLC: suitable SMILES string O.OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C(=O)O[Ca]OC(=O)[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO InChI 1S/2C6H12O7.Ca.H2O/c2*7-1-2(8)3(9)4(10)5(11)6(12)13;;/h2*2-5,7-11H,1H2,(H,12,13);;1H2/q;;+2;/p-2/t2*2-,3-,4+,5-;;/m11../s1 InChI key XLNFVCRGJZBQGX-XRDLMGPZSA-L
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Calcium D-saccharate tetrahydrate
Empirical Formula (Hill Notation): C6H8CaO8 · 4H2O CAS Number: 5793-89-5 Molecular Weight: 320.26 Beilstein/REAXYS Number: 3821334 EC Number: 227-334-1 MDL number: MFCD00150704 PubChem Substance ID: 57647917
Кат. номер 21236-25G 21236-100G ApplicationD-Saccharate (D-glucaric acid) is used to study its potential chemopreventive properties and anti-oxidative properties at the level of peroxynitrite-induced damages.Biochem/physiol ActionsCalcium glucarate is a constituent of many fruits (apples, citrus fruits) and cruciferous vegetables. Inhibits β-glucuronidase, a phase II enzyme that is elevated in some hormone-dependent cancers of the breast, prostate, and colon.ПараметрыQuality Level 200, biological source synthetic assay 98.5-102% (KT) form powder optical activity []20/D +20.5±2°, c = 6% in 5 M HCl storage temp. room temp SMILES string [H]O[H].[H]O[H].[H]O[H].[H]O[H].O[C@H]1[C@H](O)[C@@H](O)C(=O)O[Ca]OC(=O)[C@H]1O InChI 1S/C6H10O8.Ca.4H2O/c7-1(3(9)5(11)12)2(8)4(10)6(13)14;;;;;/h1-4,7-10H,(H,11,12)(H,13,14);;4*1H2/q;+2;;;;/p-2/t1-,2-,3-,4+;;;;;/m0...../s1 InChI key ZQWFSIZRQANUDA-WQMSYZFBSA-L
Safety InformationPersonal Protective Equipment dust mask type N95 (US),, Eyeshields,, Gloves, RIDADR NONH for all modes of transport WGK Germany WGK 3 Flash Point F Not applicable Flash Point C Not applicable Узнать цену -
Calcium L-ascorbate dihydrate
Empirical Formula (Hill Notation): C12H14CaO12 · 2H2O CAS Number: 5743-28-2 Molecular Weight: 426.34 EC Number: 227-261-5 MDL number: MFCD00149216 PubChem Substance ID: 24862094 NACRES: NA.22
Кат. номер 359645-100G 359645-25G 359645-500G ПараметрыQuality Level 100, assay 99% optical activity []20/D +95°, c = 5 in H2O mp 166 °C (dec.) (lit.) SMILES string [H]O[H].[H]O[H].OC[C@H](O)[C@H]1OC(=O)C(O)=C1O[Ca]OC2=C(O)C(=O)O[C@@H]2[C@@H](O)CO InChI 1S/2C6H8O6.Ca.2H2O/c2*7-1-2(8)5-3(9)4(10)6(11)12-5;;;/h2*2,5,7-10H,1H2;;2*1H2/q;;+2;;/p-2/t2*2-,5+;;;/m00.../s1 InChI key RGJHWLDSRIHFKY-FWCDDDAWSA-L
Safety InformationPersonal Protective Equipment Eyeshields,, Gloves,, type N95 (US), RIDADR NONH for all modes of transport WGK Germany WGK 1 Flash Point F 572.0 °F - closed cup Flash Point C 300.00 °C - closed cup Узнать цену -
Calcium lactobionate monohydrate L3375-100G
Empirical Formula (Hill Notation): C12H21O12 · 0.5Ca · H2O CAS Number: 110638-68-1 Molecular Weight: 395.34 EC Number: 225-668-2 MDL number: MFCD10567434 PubChem Substance ID: 24896338 NACRES: NA.25 ПараметрыQuality Level 200, assay 98.0-102.0% (EDTA titration) form powder optical activity [α]20/D 22.5 to 24.5 °, c = 3% (w/v) in water SMILES string O.OC[C@@H](O)[C@@H](O[C@@H]1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O)[C@H](O)[C@@H](O)C(=O)O[Ca]OC(=O)[C@H](O)[C@@H](O)[C@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O)[C@H]2O)[C@H](O)CO InChI 1S/2C12H22O12.Ca.H2O/c2*13-1-3(15)10(7(18)8(19)11(21)22)24-12-9(20)6(17)5(16)4(2-14)23-12;;/h2*3-10,12-20H,1-2H2,(H,21,22);;1H2/q;;+2;/p-2/t2*3-,4-,5+,6+,7-,8-,9-,10-,12+;;/m11../s1 InChI key LIUNXXYNUIALAY-BSLBODANSA-L
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Calcium lactobionate monohydrate
Empirical Formula (Hill Notation): C24H42CaO24 · 2H2O CAS Number: 110638-68-1 Molecular Weight: 790.68 Beilstein/REAXYS Number: 3834794 EC Number: 225-668-2 MDL number: MFCD16661223 PubChem Substance ID: 57647911 NACRES: NA.22
Кат. номер 21190-500G-F 21190-100G-F ПараметрыQuality Level 200, assay 98.0% (KT) optical activity []20/D +23.5±1°, c = 3% in H2O SMILES string O.O.OC[C@@H](O)[C@@H](O[C@@H]1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O)[C@H](O)[C@@H](O)C(=O)O[Ca]OC(=O)[C@H](O)[C@@H](O)[C@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O)[C@H]2O)[C@H](O)CO InChI 1S/2C12H22O12.Ca.2H2O/c2*13-1-3(15)10(7(18)8(19)11(21)22)24-12-9(20)6(17)5(16)4(2-14)23-12;;;/h2*3-10,12-20H,1-2H2,(H,21,22);;2*1H2/q;;+2;;/p-2/t2*3-,4-,5+,6+,7-,8-,9-,10-,12+;;;/m11.../s1 InChI key FALNADDKNDADFQ-WNSOHMSISA-L
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Callistephin chloride
Empirical Formula (Hill Notation): C21H21ClO10 CAS Number: 18466-51-8 Molecular Weight: 468.84 MDL number: MFCD00017578 PubChem Substance ID: 329757950 NACRES: NA.25
Кат. номер 53489-1MG 53489-5MG Biochem/physiol ActionsCallistephin chloride is an anthocyanin which can be found in berries, for example in strawberries and chokeberries. Is has antioxidant activity and is examined for its neuroprotective properties.PackagingBottomless glass bottle. Contents are inside inserted fused cone.ПараметрыQuality Level 100, biological source synthetic assay ≥95.0% (HPLC) form powder shipped in wet ice storage temp. −20°C SMILES string [Cl-].OC[C@H]1O[C@@H](Oc2cc3c(O)cc(O)cc3[o+]c2-c4ccc(O)cc4)[C@H](O)[C@@H](O)[C@@H]1O InChI 1S/C21H20O10.ClH/c22-8-16-17(26)18(27)19(28)21(31-16)30-15-7-12-13(25)5-11(24)6-14(12)29-20(15)9-1-3-10(23)4-2-9;/h1-7,16-19,21-22,26-28H,8H2,(H2-,23,24,25);1H/t16-,17-,18+,19-,21-;/m1./s1 InChI key CAHGSEFWVUVGGL-UBNZBFALSA-N
Safety InformationRIDADR NONH for all modes of transport WGK Germany WGK 3 Flash Point F Not applicable Flash Point C Not applicable Узнать цену -
Chondroitin disaccharide di-0S sodium salt
Empirical Formula (Hill Notation): C14H20NNaO11 Linear Formula: C14H20NO11Na CAS Number: 136132-69-9 Molecular Weight: 401.30 MDL number: MFCD00133173 PubChem Substance ID: 24892657
Кат. номер C3920-5MG C3920-10MG General descriptionChondroitin, a glucosaminoglycan (GAG), is a polysaccharide chain of alternating units of N-acetylgalactosamine (GalNAc) and glucuronic acid (GlcA) that can be sulfated on the either or both GalNAc and GlcA units. Chondroitin and its sulfates are frequently attached to proteins to form proteoglycans.ApplicationChondroitin disaccharide di-0S may be used as a substrate for the identification and characterization of enzymes such as Clostridium perfringens unsaturated glucuronyl hydrolase. Chondroitin disaccharide di-0S may be used as a reference compound in the analysis of chondroitin disaccharide sulfates.Packaging5 mg in glass bottleOther NotesUA = 4-deoxy-L-threo-hex-4-enopyranosyluronic acid; GalNAc = N-acetyl-D-galactosamineПараметрыQuality Level 200, assay 95% (HPLC) form powder solubility H2O: soluble 10 mg/mL, clear, colorless storage temp. 20°C SMILES string [Na].CC(=O)NC(C=O)C(OC1OC(=CC(O)C1O)C(O)=O)C(O)C(O)CO InChI 1S/C14H21NO11.Na.H/c1-5(18)15-6(3-16)12(10(21)8(20)4-17)26-14-11(22)7(19)2-9(25-14)13(23)24;;/h2-3,6-8,10-12,14,17,19-22H,4H2,1H3,(H,15,18)(H,23,24);; InChI key SDRQEYWJTBWGNE-UHFFFAOYSA-N
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Chondroitin sulfate B sodium salt
CAS Number: 54328-33-5 MDL number: MFCD00151683 NACRES: NA.25
Кат. номер C3788-25MG C3788-100MG General descriptionChondroitin, a glucosaminoglycan (GAG), is a polysaccharide chain of alternating units of N-acetylgalactosamine (GalNAc) and glucuronic acid (GlcA) that can be sulfated on the either or both GalNAc and GlcA units. Chondroitin and its sulfates are frequently attached to proteins to form proteoglycans. Chondroitin sulfate B (Dermatam sulfate) is a component of proteoglycans such as decorin, biglycan and versican. Chondroitin sulfate B is used to study β peptide (1-42) cytotoxicity.ApplicationChondroitin sulfate B may be used to study its roles as a biomolecule receptor, mediator of cell signaling and cell binding molecule. It may be used to compare its properties to those of chondroitin sulfate A and chondroitin sulfate C. Chondroitin sulfate B is used to study β peptide(1-42) cytotoxicity.Packaging25, 100 mg in poly bottleBiochem/physiol ActionsAs a large, negatively charged, hydrophilic molecule that is too inflexible to fold into a compact globular structure, chondroitin sulfate molecules form porous hydrated gels, providing mechanical support to tissue and allowing rapid diffusion of water-soluble molecules and migration of cells.ComponentsChondroitin Sulfate B is an acidic mucopolysaccharide found in cartilage, skin, cornea, and umbilical cord. It is composed of alternating N-acetylgalactosamine, L-iduronic acid, and sulfate residues in equimolar quantities where carbon 4 of the N-acetylgalactosamines is sulfated.CautionStore this product at 2-8°C.Preparation NoteThis product is soluble in water at 100 mg/mL.Параметрыbiological source Porcine intestinal mucosa Quality Level 200, assay 90% form lyophilized powder solubility H2O: 5 mg/mL, clear, colorless storage temp. 2-8°C
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Chondroitin sulfate sodium salt from bovine cartilage C6737-5G
PubChem Substance ID: 24892886 NACRES: NA.25 General descriptionChondroitin, a glucosaminoglycan (GAG), is a polysaccharide chain of alternating units of N-acetylgalactosamine (GalNAc) and glucuronic acid (GlcA) that can be sulfated on the either or both GalNAc and GlcA units. Chondroitin and its sulfates are frequently attached to proteins to form proteoglycans.ApplicationChondroitin sulfate, a glucosaminoglycan (GAG) polysaccharide chain of alternating units of N-acetylgalactosamine (GalNAc) and glucuronic acid (GlcA), is used in a wide variety of areas of research including bioengineering. Chondroitin sulfate may be used as a biomaterial copolymer or surface derivatization reagent in the development of drug delivery vehicles, tissue engineering devices and bioscaffolds. Chondroitin sulfate may be used for the development of biocompatible structures such as hydrogels, sponges, biofilms, microspheres and micelles.Packaging5 g in poly bottleBiochem/physiol ActionsAs a large, negatively charged, hydrophilic molecule that is too inflexible to fold into a compact globular structure, chondroitin sulfate molecules form porous hydrated gels, providing mechanical support to tissue and allowing rapid diffusion of water-soluble molecules and migration of cells.ComponentsChondroitin is an acidic mucopolysaccharide found in cartilage, skin, cornea, and umbilical cord. It is composed of alternating N-acetylgalactosamine, D-glucuronic acid, and sulfate residues in equimolar quantities that can be sulfated on either of its subunits. Sulfation can occur at the 6 and/or 4-position of the galactosamine moiety, with potential for any individual disaccharide unit to be 6-sulfated, 4-sulfated, 4,6-disulfated, or unsulfated.CautionStore this product at 2-8°C.Preparation NoteThis product is soluble in water at 100 mg/mL.ПараметрыQuality Level 200, grade standard (for CPC (cetylpyridinium chloride) titration) assay 98-102% (CPC, titration) form powder optical activity []20/D -30 to -20 °, c = 5% (w/v) in water solubility H2O: soluble 50 mg/mL, clear to hazy, colorless to faintly yellow storage temp. 2-8°C SMILES string [Na+].CC(=O)N[C@H]1[C@H](O)O[C@H](CO)[C@H](OS([O-])(=O)=O)[C@@H]1O[C@H]2O[C@@H]([C@H](O)[C@@H](O)[C@@H]2O)C(O)=O
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Chondroitin sulfate sodium salt from shark cartilage
CAS Number: 9082-07-9 PubChem Substance ID: 24892689 NACRES: NA.25
Кат. номер C4384-5G C4384-25G C4384-250MG C4384-1G General descriptionChondroitin, a glucosaminoglycan (GAG), is a polysaccharide chain of alternating units of N-acetylgalactosamine (GalNAc) and glucuronic acid (GlcA) that can be sulfated on the either or both GalNAc and GlcA units. Chondroitin and its sulfates are frequently attached to proteins to form proteoglycans.ApplicationChondroitin sulfate is used in a wide variety of areas of research such as bioengineering. Chondroitin sulfate may be used as a biomaterial copolymer or surface derivatization reagent in the development of drug delivery vehicles, tissue engineering devices and bioscaffolds. Chondroitin sulfate may be used for the development of biocompatible structures such as hydrogels, sponges, biofilms, microspheres and micelles.
Chondroitin appears to play a regulatory role for chondrocytes, neural cells, and some tumor cells. Chondroitin sulfate B is used to study peptide (1-42) cytotoxicity.Biochem/physiol ActionsChondroitin, a glucosaminoglycan (GAG), is a natural polymer of β-glucuronic acid-(1→ 3)N-acetyl-β-galactosamine [β-GlcA-(1→3)-GalNAc-(1→4)]. Sulfation may occur at the 6-position and/or 4-position of the galactosamine moiety, with the potential of any individual disaccharide unit to be 6-sulfated, 4-sulfated, 4,6-disulfated, or unsulfated.
As a large, negatively charged, hydrophilic molecule that is too inflexible to fold into a compact globular structure, chondroitin sulfate molecules form porous hydrated gels, providing mechanical support to tissue and allowing rapid diffusion of water-soluble molecules and migration of cells.ComponentsChondroitin is an acidic mucopolysaccharide found in cartilage, skin, cornea, and umbilical cord. It is composed of alternating N-acetylgalactosamine, D-glucuronic acid, and sulfate residues in equimolar quantities that can be sulfated on either of its subunits. Sulfation can occur at the 6 and/or 4-position of the galactosamine moiety, with potential for any individual disaccharide unit to be 6-sulfated, 4-sulfated, 4,6-disulfated, or unsulfated.CautionStore this product at 2-8°C.Preparation NoteThis product is soluble in water at 100 mg/mL.Analysis NoteRatio of β-GlcA-(1→3)-GalNAc-6-sulfate to β-GlcA-(1→3)-GalNAc-4-sulfate is determined by HPLC after enzymatic degradation.ПараметрыQuality Level 200, biological source shark (cartilage) form powder storage temp. 2-8°C InChI 1S/C13H21NO15S/c1-2(15)14-3-8(7(19)13(28-11(3)22)29-30(23,24)25)26-12-6(18)4(16)5(17)9(27-12)10(20)21/h3-9,11-13,16-19,22H,1H3,(H,14,15)(H,20,21)(H,23,24,25)/t3-,4+,5+,6-,7-,8-,9+,11-,12-,13-/m1/s1 InChI key KXKPYJOVDUMHGS-OSRGNVMNSA-N
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Cichoriin SMB00919-25MG
Empirical Formula (Hill Notation): C15H16O9 CAS Number: 531-58-8 Molecular Weight: 340.28 MDL number: MFCD03840467 General descriptionCichoriin is a glycoside found in chicory (Cichorium intybus) (1),ApplicationMetabolomics researchПараметрыassay ≥95% (HPLC) form powder color off-white to beige storage temp. 2-8°C InChI 1S/C15H16O9/c16-5-10-12(19)13(20)14(21)15(24-10)23-9-4-8-6(3-7(9)17)1-2-11(18)22-8/h1-4,10,12-17,19-21H,5H2/t10-,12-,13+,14-,15-/m1/s1 InChI key WNBCMONIPIJTSB-TVKJYDDYSA-N
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Cornin SMB00398-5MG
Empirical Formula (Hill Notation): C17H24O10 CAS Number: 548-37-8 Molecular Weight: 388.37 Beilstein/REAXYS Number: 57895 MDL number: MFCD00017414 PubChem Substance ID: 329824990 NACRES: NA.25 Packaging5 mg in glass bottleBiochem/physiol ActionsCornin is an iridoid glucoside with hepato-protective and sleep promoting properties.ПараметрыQuality Level 200, assay ≥98% (HPLC) form powder storage temp. 2-8°C SMILES string [H][C@@]12[C@@H](C)CC(=O)[C@]1([H])C(=CO[C@H]2O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)C(=O)OC InChI 1S/C17H24O10/c1-6-3-8(19)11-7(15(23)24-2)5-25-16(10(6)11)27-17-14(22)13(21)12(20)9(4-18)26-17/h5-6,9-14,16-18,20-22H,3-4H2,1-2H3/t6-,9+,10+,11-,12+,13-,14+,16-,17-/m0/s1 InChI key HLXRWTJXGMHOFN-XJSNKYLASA-N
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D-()-Fructose
Empirical Formula (Hill Notation): C6H12O6 CAS Number: 57-48-7 Molecular Weight: 180.16 Beilstein/REAXYS Number: 1239004 EC Number: 200-333-3 MDL number: MFCD00148910 PubChem Substance ID: 329757342 NACRES: NA.21
Кат. номер 47748-VAR-F 47748-25KG-F 47748-1KG-F ApplicationD-(−)-Fructose has been used as a test compound for investigating the enzyme that catalyzes the synthesis of activator for phosphofructokinase termed “activation factor” by utilizing ATP and D-fructose-6-P.Packaging1 kg in poly bottleBiochem/physiol ActionsD-(−)-Fructose can enhance mood and gastrointestinal disturbances in fructose malabsorbers. It also possess metabolic and endocrine impact that shows that increased consumption of fructose is a contributing factor in the development of obesity and the accompanying metabolic abnormalities observed in the insulin resistance syndrome.ПараметрыQuality Level 100, Agency/Method USP/NF, tested according to Ph. Eur. mp 119-122 °C (dec.) (lit.) solubility alcohol: soluble 1 gm in 15 ml, methanol: soluble 1 gm in 14 ml, H2O: freely soluble, acetone: freely soluble (Hot), acetone: slightly soluble, pyridine: soluble SMILES string OC[C@@H](O)[C@@H](O)[C@H](O)C(=O)CO InChI 1S/C6H12O6/c7-1-3(9)5(11)6(12)4(10)2-8/h3,5-9,11-12H,1-2H2/t3-,5-,6-/m1/s1 InChI key BJHIKXHVCXFQLS-UYFOZJQFSA-N
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D-()-Isoascorbic acid
Empirical Formula (Hill Notation): C6H8O6 CAS Number: 89-65-6 Molecular Weight: 176.12 Beilstein/REAXYS Number: 84271 EC Number: 201-928-0 MDL number: MFCD00005378 PubChem Substance ID: 24888398 NACRES: NA.22
Кат. номер 856061-100G 856061-500G 856061-5G ПараметрыQuality Level 200, assay 98% optical activity []25/D 16.8°, c = 2 in H2O mp 169-172 °C (dec.) (lit.) SMILES string [H][C@@]1(OC(=O)C(O)=C1O)[C@H](O)CO InChI 1S/C6H8O6/c7-1-2(8)5-3(9)4(10)6(11)12-5/h2,5,7-10H,1H2/t2-,5-/m1/s1 InChI key CIWBSHSKHKDKBQ-DUZGATOHSA-N
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D-()-Lyxose
Empirical Formula (Hill Notation): C5H10O5 CAS Number: 1114-34-7 Molecular Weight: 150.13 Beilstein/REAXYS Number: 1723083 EC Number: 214-212-8 MDL number: MFCD00064362 PubChem Substance ID: 24853173 NACRES: NA.22
Кат. номер 220477-5G 220477-1G Packaging5 g in glass bottleOther NotesTandem Mass Spectrometry data independently generated by Scripps Center for Metabolomics is available to view or download in PDF. 220477.pdf , Tested metabolites are featured on Scripps Center for Metabolomics METLIN Metabolite Database. To learn more, visit sigma.com/metlin.,ПараметрыQuality Level 200, assay 99% optical activity []25/D -15.8°, c = 4 in H2O mp 108-112 °C (lit.) SMILES string O[C@@H]1COC(O)[C@@H](O)[C@H]1O InChI 1S/C5H10O5/c6-2-1-10-5(9)4(8)3(2)7/h2-9H,1H2/t2-,3+,4+,5?/m1/s1 InChI key SRBFZHDQGSBBOR-AGQMPKSLSA-N
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D-()-Ribose
Empirical Formula (Hill Notation): C5H10O5 CAS Number: 50-69-1 Molecular Weight: 150.13 Beilstein/REAXYS Number: 1723081 EC Number: 200-059-4 MDL number: MFCD00135453 PubChem Substance ID: 24899349 NACRES: NA.22
Кат. номер R1757-25G-A R1757-10G-A R1757-100G-A R1757-1G-A ПараметрыQuality Level 100, assay 98% optical activity []20/D 19.7°, c = 4 in H2O mp 88-92 °C (lit.) SMILES string OC[C@@H](O)[C@@H](O)[C@@H](O)C([H])=O InChI 1S/C5H10O5/c6-1-3(8)5(10)4(9)2-7/h1,3-5,7-10H,2H2/t3-,4+,5-/m0/s1 InChI key PYMYPHUHKUWMLA-LMVFSUKVSA-N
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D-()-Salicin
Empirical Formula (Hill Notation): C13H18O7 CAS Number: 138-52-3 Molecular Weight: 286.28 Beilstein/REAXYS Number: 89593 EC Number: 205-331-6 MDL number: MFCD00006590 PubChem Substance ID: 24899442 NACRES: NA.25
Кат. номер S0625-100G S0625-25G S0625-5G S0625-10G General descriptionSalicin is a non-phenolic glucosidic compound extracted from meadowsweet (Filipendula ulmaria L). It is majorly used as a substitute for quinine. Salicin can be used as a therapeutic for patients suffering from rheumatic fever. Salicin acts a metabolic precursor for salicylic acid. It is a novel phytochemical that exhibits immunological cross functions in plants and humans. Salicin facilitates growth and reproduction in plants. In addition, It also protects plants against biotic and abiotic stress.ApplicationD-(-)-Salicin has been used:- to study its in vitro anticoagulant and antiplatelet activities
- as a standard in high performance liquid chromatography method (HPLC) for quantitation of salicin from willow plant
- as a tastant in taste threshold assay
- as a constituent of nutrient agar-salicin medium for selective isolation of Lactobacillus paracasei
Packaging5, 25, 100 g in poly bottleBiochem/physiol ActionsD-()-Salicin exerts anti-rheumatism and anti-inflammatory activities. It inhibits lipopolysaccharide (LPS) induced inflammation in in vitro and in vivo studies. It regulates different signaling pathways such as nuclear factor kappa B (NF-B) and mitogen-activated protein kinase (MAPK). It also regulates cytokines concentration such as tumor necrosis factor-alpha(TNF-), interleukin-1, interleukin-6, and interleukin-10.ПараметрыQuality Level 200, assay 99% (GC) SMILES string OC[C@H]1O[C@@H](Oc2ccccc2CO)[C@H](O)[C@@H](O)[C@@H]1O InChI 1S/C13H18O7/c14-5-7-3-1-2-4-8(7)19-13-12(18)11(17)10(16)9(6-15)20-13/h1-4,9-18H,5-6H2/t9-,10-,11+,12-,13-/m1/s1 InChI key NGFMICBWJRZIBI-UJPOAAIJSA-N
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D-(+)-Arabitol
Empirical Formula (Hill Notation): C5H12O5 CAS Number: 488-82-4 Molecular Weight: 152.15 Beilstein/REAXYS Number: 1720520 EC Number: 207-686-2 MDL number: MFCD00004709 PubChem Substance ID: 24890762 NACRES: NA.25
Кат. номер A3381-100G A3381-250G A3381-25G A3381-10G A3381-5G A3381-1G ApplicationD-Arabitol, a rare sugar alcohol, is a substrate used to identify, differentiate and characterize enzyme such as the gluconobacter oxydans dehydrogenase(s), Gox2181, hyperthermophilic D-arabitol dehydrogenase from Thermotoga maritime and NAD-dependent D-arabitoldehydrogenase from acetic acid bacterium, Acetobacter suboxydans.Packaging25, 100, 250 g in poly bottleBiochem/physiol ActionsUsed to produce xylitol via biotransformation.ПараметрыQuality Level 200, assay 99% sweetness 0.7 x sucrose SMILES string OC[C@@H](O)C(O)[C@H](O)CO InChI 1S/C5H12O5/c6-1-3(8)5(10)4(9)2-7/h3-10H,1-2H2/t3-,4-/m1/s1 InChI key HEBKCHPVOIAQTA-QWWZWVQMSA-N
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D-(+)-chiro-Inositol
Empirical Formula (Hill Notation): C6H12O6 CAS Number: 643-12-9 Molecular Weight: 180.16 EC Number: 211-394-0 MDL number: MFCD00272608 PubChem Substance ID: 24870460 NACRES: NA.22
Кат. номер 468045-1G 468045-100MG 468045-25MG ApplicationThe inositols and their phosphates have been used in the development of metabolically stable insulin mediators, inhibitors, and modulators of important metabolic functions such as glycolysis. Inositols are stable to degradative enzymes in vivo because they lack a hydrolytically labile glycosidic linkage.Packaging1 g in glass bottle
100 mg in glass insertПараметрыQuality Level 100, assay 95% optical activity []23/D +60°, c = 1.2 in H2O optical purity ee: 99% (GLC) mp 230 °C (lit.) storage temp. 2-8°C SMILES string O[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@H](O)[C@@H]1O InChI 1S/C6H12O6/c7-1-2(8)4(10)6(12)5(11)3(1)9/h1-12H/t1-,2-,3-,4-,5+,6+/m0/s1 InChI key CDAISMWEOUEBRE-LKPKBOIGSA-N
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D-(+)-Galactosamine hydrochloride
Empirical Formula (Hill Notation): C6H13NO5 · HCl CAS Number: 1772-03-8 Molecular Weight: 215.63 Beilstein/REAXYS Number: 3697825 EC Number: 217-198-1 MDL number: MFCD00135830 PubChem Substance ID: 24894912 NACRES: NA.25
Кат. номер G0500-10MG G0500-5G G0500-25G G0500-100MG G0500-1G G0500-500MG ApplicationD-(+)-Galactosamine (D-chondrosamine) is used with lipopolysaccharides (LPS) to induce models of acute hepatic failure (LPS/D-GalN-induced liver injury, hepatitis) for therapeutic research to find new drugs.Packaging5, 25 g in poly bottle
10 mg in glass bottleПараметрыQuality Level 200, biological source shark (cartilage) assay 99% form powder application(s) HPLC: suitable impurities 0.5% Glucosamine (HPAE) mp 172-180 °C solubility H2O: 50 mg/mL, clear to slightly hazy, colorless to very faintly yellow SMILES string Cl.N[C@@H](C=O)[C@@H](O)[C@@H](O)[C@H](O)CO InChI 1S/C6H13NO5.ClH/c7-3(1-8)5(11)6(12)4(10)2-9;/h1,3-6,9-12H,2,7H2;1H/t3-,4+,5+,6-;/m0./s1 InChI key CBOJBBMQJBVCMW-NQZVPSPJSA-N
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D-(+)-Galactose
Empirical Formula (Hill Notation): C6H12O6 CAS Number: 59-23-4 Molecular Weight: 180.16 Beilstein/REAXYS Number: 1724619 EC Number: 200-416-4 MDL number: MFCD00151230 PubChem Substance ID: 57647466 NACRES: NA.21
Кат. номер 15522-100G-R 15522-VAR-R 15522-250G-R 15522-6X100G-R 15522-VAR-F 15522-6X250G-R 15522-1KG-R 15522-6X1KG-R 15522-1.5KG-R ApplicationD-(+)-Galactose was used for examining the specificity of staining with SBA-FITC during labeling of cells for fluorescence-activated cell sorting (FACS). It was used for selecting the transformed strains of S. cerevisiae.Biochem/physiol ActionsGalactose is a simple monosaccharide that serves as an energy source and as an essential component of glycolipids and glycoproteins. Galactose contributes to energy metabolism via its conversion to glucose by the enzymes that constitute the Leloir pathway. Defects in the genes encoding these proteins lead to the metabolic disorder galactosemia.
Galactose is a monosaccharide sugar and is the natural antigen present on the blood cells. It induces memory loss, neurodegeneration as well as oxidative damage in mice due to systemic exposure.Параметрыquality meets analytical specification of Ph. Eur., BP Quality Level 200, application(s) IR spectroscopy: suitable impurities acid. or alk. react. impurities, in accordance, microbiological impurity, in accordance, residual solvents, in accordance, 1.0% water (Karl Fischer) mp 168-170 °C (lit.) solubility H2O: soluble 180 g/L at 20 °C suitability in accordance for appearance of solution, in accordance for identity (IR) Featured Industry Pharmaceutical (small molecule) SMILES string OC[C@@H](O)[C@H](O)[C@H](O)[C@@H](O)C=O InChI 1S/C6H12O6/c7-1-3(9)5(11)6(12)4(10)2-8/h1,3-6,8-12H,2H2/t3-,4+,5+,6-/m0/s1 InChI key GZCGUPFRVQAUEE-KCDKBNATSA-N
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D-(+)-Galacturonic acid monohydrate
Empirical Formula (Hill Notation): C6H10O7 · H2O CAS Number: 91510-62-2 Molecular Weight: 212.15 Beilstein/REAXYS Number: 1727087 EC Number: 211-682-6 MDL number: MFCD00071585 PubChem Substance ID: 329757364 NACRES: NA.22
Кат. номер 48280-VAR-F 48280-5G-F 48280-25G-F ПараметрыQuality Level 200, assay 97.0% (T), 97.0% optical activity []20/D +53±2°, 5 hr, c = 10% in H2O SMILES string O.OC1O[C@@H]([C@H](O)[C@H](O)[C@H]1O)C(O)=O InChI 1S/C6H10O7.H2O/c7-1-2(8)4(5(10)11)13-6(12)3(1)9;/h1-4,6-9,12H,(H,10,11);1H2/t1-,2+,3+,4-,6?;/m0./s1 InChI key BGHPCEJXDOGRGW-KSSASCOMSA-N
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D-(+)-Gluconic acid -lactone
Empirical Formula (Hill Notation): C6H10O6 CAS Number: 90-80-2 Molecular Weight: 178.14 Beilstein/REAXYS Number: 83286 EC Number: 202-016-5 MDL number: MFCD00006647 PubChem Substance ID: 24895183 NACRES: NA.25
Кат. номер G4750-1KG G4750-500G G4750-100G General descriptionD-(+)-Gluconic acid -lactone (GDL) is soluble in water and hydrolyzes into gluconic acid spontaneously and homogeneously lowers the pH. Quinoprotein glucose dehydrogenase converts D-glucose to GDL which gradually lowers the pH and transcriptionally controls the prodigiosin production. GDL is commonly used in the food industry to cause gelation of sodium caseinate by acidification. GDL helps to overcome the difficulties and variations of using starter bacterial cultures.ApplicationD-(+)-Gluconic acid -lactone has been used in the preparation of cold set gels, and hydrogels.Packaging1 kg in poly bottle
100, 500 g in poly bottleBiochem/physiol ActionsGlucono-d-lactone increased the doubling time and activated enzymes involved in the oxidative pentose phosphate pathway of Saccharomyces cerevisiae.Other NotesTandem Mass Spectrometry data independently generated by Scripps Center for Metabolomics is available to view or download in PDF. G4750.pdf , Tested metabolites are featured on Scripps Center for Metabolomics METLIN Metabolite Database. To learn more, visit sigma.com/metlin.,ПараметрыQuality Level 200, biological source microbial assay 99.0% form powder application(s) gas chromatography (GC): suitable mp 160 °C (dec.) (lit.) SMILES string OC[C@H]1OC(=O)[C@H](O)[C@@H](O)[C@@H]1O InChI 1S/C6H10O6/c7-1-2-3(8)4(9)5(10)6(11)12-2/h2-5,7-10H,1H2/t2-,3-,4+,5-/m1/s1 InChI key PHOQVHQSTUBQQK-SQOUGZDYSA-N
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D-(+)-Glucosamine hydrochloride
Empirical Formula (Hill Notation): C6H13NO5 · HCl CAS Number: 66-84-2 Molecular Weight: 215.63 Beilstein/REAXYS Number: 4157370 EC Number: 200-638-1 MDL number: MFCD00135831 PubChem Substance ID: 24895187 NACRES: NA.25
Кат. номер 2530120 G4875-100G G4875-10MG G4875-25G G4875-500G G4875-1KG ApplicationD-(+)-Glucosamine hydrochloride has been used:- as a standard to quantify and express chitin content as glucosamine equivalents.
- to stimulate cells with glucose in the presence of glucosamine
Packaging10 mg in autosample vial
25, 100, 500 g in poly bottle
1 kg in poly bottleBiochem/physiol ActionsGlucosamine, an amino sugar, is the precursor of the hexosamine biosynthetic pathway leading to the formation of UDP-N-acetylglucosamine (UDP-GlcNAc), which is then used for making glycosaminoglycans, proteoglycans, and glycolipids. D-(+)-Glucosamine inhibits the coaggregation of Candida yeast species with the bacterial strain S. salivarius.Параметрыbiological source Aspergillus niger Quality Level 200 assay 99% form crystalline application(s) HPLC: suitable mp 190-194 °C (dec.) (lit.) SMILES string Cl.N[C@H]1C(O)O[C@H](CO)[C@@H](O)[C@@H]1O InChI 1S/C6H13NO5.ClH/c7-3-5(10)4(9)2(1-8)12-6(3)11;/h2-6,8-11H,1,7H2;1H/t2-,3-,4-,5-,6?;/m1./s1 InChI key QKPLRMLTKYXDST-NSEZLWDYSA-N
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D-(+)-Glucose
Empirical Formula (Hill Notation): C6H12O6 CAS Number: 50-99-7 Molecular Weight: 180.16 Beilstein/REAXYS Number: 1724615 EC Number: 200-075-1 MDL number: MFCD00063774 PubChem Substance ID: 24895199 NACRES: NA.75
Кат. номер G5146-1KG G5146-10KG G5146-100G G5146-5KG General descriptionGlycogen phosphorylase (PYG) exists as brain and muscle isoform. It is expressed in astrocytes and neurons respectively. The PYGM gene is mapped to human chromosome 11q13.1.ApplicationD-(+)-Glucose has been used in cell engineering. It has also been used to perform oral glucose tolerance test.Packaging1 kg in poly bottle
10 kg in poly drumBiochem/physiol ActionsGlycogen phosphorylase, muscle associated (PYGM), is an important contributor to glycogenolysis. Down regulation of PYGM gene is observed in schizophrenia. Mutation in PYGM leads to McArdle disease, a glycogen storage disorder. The PYGM gene is significantly associated with energy production.Legal InformationHybri-Max is a trademark of Sigma-Aldrich Co. LLCПараметрыbiological source maize Quality Level 200, grade Hybri-Max™ product line BioReagent assay 99.5% form powder application(s) cell culture | hybridoma: suitable impurities endotoxin, tested mp 150-152 °C (lit.) solubility H2O: 2g + 15 mL, clear, colorless SMILES string OC[C@H]1O[C@H](O)[C@H](O)[C@@H](O)[C@@H]1O InChI 1S/C6H12O6/c7-1-2-3(8)4(9)5(10)6(11)12-2/h2-11H,1H2/t2-,3-,4+,5-,6+/m1/s1 InChI key WQZGKKKJIJFFOK-DVKNGEFBSA-N Gene Information human ... PYGM(5837)
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D-(+)-Glucose monohydrate
Empirical Formula (Hill Notation): C6H12O6 · H2O CAS Number: 14431-43-7 Molecular Weight: 198.17 Beilstein/REAXYS Number: 5250278 EC Number: 218-914-5 MDL number: MFCD00149450 PubChem Substance ID: 57647555 NACRES: NA.21
Кат. номер 16301-50KG 16301-6X1KG 16301-250G 16301-VAR 16301-25KG 16301-6X2.5KG 16301-1KG 16301-2.5KG 16301S-5KG 16301-6X250G 16301-1.5KG ApplicationD-(+)-Glucose monohydrate has been used as a test compound for studying its dehydration kinetics by using THz time-domain spectroscopy (THz-TDS).Biochem/physiol ActionsD-(+)-Glucose is a common natural sugar involved in key cellular processes of energy production, glycosylation and formation of glycans that provide structure to cells. Glucose is involved in post-translational modifications of proteins by glycation or non-enzymatic glycosylation of proteins at the lysine residues. Glycation is detrimental and results in complications associated with diabetes mellitus, alzheimer′s disease, aging and cataract.Параметрыassay 97.5-102.0% anhydrous basis (HPLC) Quality Level 200, optical activity []20/D +52.5 to +53.3°, c = 10% in H2O (calc. on anhydrous subst.) quality meets analytical specification of Ph. Eur., BP, Ph Fran. impurities residual solvents, complies, 7.0-9.5% water (Karl Fischer) ign. residue 0.1% (as SO4) solubility H2O: 10g/5 mL, clear, colorless anion traces chloride (Cl-): 100 mg/kg, sulfite (SO32-): 15 ppm cation traces Al: 0.5 mg/kg, As: 1 mg/kg, Ba:, in accordance, Ca: 200 mg/kg, Pb: 0.5 mg/kg SMILES string O.OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C=O InChI 1S/C6H12O6.H2O/c7-1-3(9)5(11)6(12)4(10)2-8;/h1,3-6,8-12H,2H2;1H2/t3-,4+,5+,6+;/m0./s1 InChI key SPFMQWBKVUQXJV-BTVCFUMJSA-N
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D-(+)-Glucose solution
Empirical Formula (Hill Notation): C6H12O6 CAS Number: 50-99-7 Molecular Weight: 180.16 Beilstein/REAXYS Number: 1281608 MDL number: MFCD00063774 PubChem Substance ID: 24895346 NACRES: NA.75
Кат. номер G8644-100ML G8644-10L General descriptionGlucose provides the primary energy source for cell metabolism. It is a main source of energy for living organisms. Glucose occurs naturally in the free state in fruits and other parts of plants. It is combined into glucosides, disaccharides, oligosaccharides, the polysaccharides (cellulose and starch), and glycogen.Other NotesThis product has been tested with cell lines to verify the product is not cytotoxic. The growth promoting capacity of this cell culture tested glucose solution was assessed at 45 mL/L in medium using appropriate cell lines.
This solution has been sterilized by filtration.ПараметрыQuality Level 400 sterility sterile-filtered product line BioXtra form solution concentration 100 g/L in H2O application(s) cell culture | mammalian: suitable impurities endotoxin, tested storage temp. room temp SMILES string OC[C@H]1O[C@H](O)[C@H](O)[C@@H](O)[C@@H]1O InChI 1S/C6H12O6/c7-1-2-3(8)4(9)5(10)6(11)12-2/h2-11H,1H2/t2-,3-,4+,5-,6+/m1/s1 InChI key WQZGKKKJIJFFOK-DVKNGEFBSA-N Gene Information human ... PYGM(5837)
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D-(+)-Glucuronic acid -lactone
Empirical Formula (Hill Notation): C6H8O6 CAS Number: 32449-92-6 Molecular Weight: 176.12 Beilstein/REAXYS Number: 83595 EC Number: 251-053-3 MDL number: MFCD00135622 PubChem Substance ID: 24888207 NACRES: NA.22
Кат. номер 851450-100G-A 851450-1KG-A 851450-25G-A General descriptionD-(+)-Glucuronic acid γ-lactone (Glucourono-γ-lactone, Glucurone or Glycurone) is a carbohydrate derivative. It converted into L-ascorbic acid in animals and human body. Its molecule contains two five-membered rings. Its crystal structure has been studied.ApplicationD-(+)-Glucuronic acid -lactone may be used in the following studies:- As starting ragent in the synthesis of 2,3,4,-tris(tert.-butyldimethysilyl) glucuronic acid trichloroethylester, required for the preparation of 1-O-acyl glucuronide of the anti-inflammatory drug ML-3000.
- Synthesis of optically active glucopyranoses.
- Synthesis of long-chain alkyl glucofuranosides.
Packaging100 g in poly bottle
1 kg in poly bottleOther NotesTandem Mass Spectrometry data independently generated by Scripps Center for Metabolomics is available to view or download in PDF. 851450.pdf , Tested metabolites are featured on Scripps Center for Metabolomics METLIN Metabolite Database. To learn more, visit sigma.com/metlin.,ПараметрыQuality Level 200, assay 99% optical activity []24/D +18.8°, c = 8 in H2O mp 172-175 °C (lit.) solubility water: soluble 25 mg/mL, clear, colorless SMILES string O=C([C@@H]([C@@H](O1)[C@H](O)[C@H](O)C1=O)O)[H] InChI 1S/C6H8O6/c7-1-2(8)5-3(9)4(10)6(11)12-5/h1-5,8-10H/t2-,3+,4-,5+/m0/s1 InChI key UYUXSRADSPPKRZ-SKNVOMKLSA-N
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D-(+)-Mannose
Empirical Formula (Hill Notation): C6H12O6 CAS Number: 3458-28-4 Molecular Weight: 180.16 Beilstein/REAXYS Number: 1564373 EC Number: 222-392-4 MDL number: MFCD00064122 PubChem Substance ID: 24897068 NACRES: NA.75
Кат. номер M6020-100G M6020-500G M6020-25G General descriptionMannose is an aldohexose carbohydrate. It is isomer of glucose with varying C2 position configuration. Majority of mannose is synthesised from its epimer glucose. It is part of the glycans present in endoplasmic reticulum (ER)/Golgi.ApplicationD-(+)-Mannose has been used:- as a reference standard in monosaccharide analysis and quantification from sea squirts Ascidiella aspersa
- as a medium component for the selection of P898012 sorgum seeds transfected with Agrobacterium
- in segmented filamentous bacterium (SFB) medium supplement for culturing human cell lines
Mannose is an aldohexose carbohydrate. This product may be used to study the effects of exogenous mannose on in vitro processes such as glycosylation.Packaging25, 100, 500 g in poly bottleBiochem/physiol ActionsMannose may be used to study the effects of exogenous mannose on in vitro processes such as glycosylation. cis-Golgi glycoproteins have high mannose and are prone to Endoglycosidase H or peptide N-glycosidase (N-glycanase) digestion.Параметрыbiological source plant (Spruce, Birch or Beech Wood, Glucose) Quality Level 200 product line BioReagent assay 99% form powder application(s) cell culture | mammalian: suitable mp 133-140 °C (lit.) solubility H2O: 50 mg/mL Featured Industry Agriculture SMILES string OC[C@H]1OC(O)[C@@H](O)[C@@H](O)[C@@H]1O InChI 1S/C6H12O6/c7-1-2-3(8)4(9)5(10)6(11)12-2/h2-11H,1H2/t2-,3-,4+,5+,6?/m1/s1 InChI key WQZGKKKJIJFFOK-QTVWNMPRSA-N
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D-(+)-Raffinose pentahydrate
Empirical Formula (Hill Notation): C18H32O16 · 5H2O CAS Number: 17629-30-0 Molecular Weight: 594.51 Beilstein/REAXYS Number: 99541 EC Number: 208-146-9 MDL number: MFCD00071590 PubChem Substance ID: 24899394 NACRES: NA.75
Кат. номер R7630-100G R7630-500G R7630-100G-9 R7630-25G ApplicationD-(+)-Raffinose pentahydrate has been used as a cryoprotectant for Caudal epididymis and zebrafish sperm.Packaging100, 500 g in poly bottleBiochem/physiol ActionsRaffinose is a galactosyl-glucosyl-fructosyl trisaccharide, which belongs to the family of oligosaccharides. It is hydrolyzed to D-galactose and sucrose by D-galactosidase. Raffinose is extracted from beet sugar molasses, cottonseed meal and seeds of food legumes. It has cell proliferative and anti-oxidative properties. Raffinose improves immune response and also has healing property.ПараметрыQuality Level 200, biological source cotton seeds product line BioReagent assay 98.0% form powder application(s) cell culture | mammalian: suitable solubility H2O: 50 mg/mL SMILES string O.O.O.O.O.OC[C@H]1O[C@H](OC[C@H]2O[C@H](O[C@]3(CO)O[C@H](CO)[C@@H](O)[C@@H]3O)[C@H](O)[C@@H](O)[C@@H]2O)[C@H](O)[C@@H](O)[C@H]1O InChI 1S/C18H32O16.5H2O/c19-1-5-8(22)11(25)13(27)16(31-5)30-3-7-9(23)12(26)14(28)17(32-7)34-18(4-21)15(29)10(24)6(2-20)33-18;;;;;/h5-17,19-29H,1-4H2;5*1H2/t5-,6-,7-,8+,9-,10-,11+,12+,13-,14-,15+,16+,17-,18+;;;;;/m1...../s1 InChI key BITMAWRCWSHCRW-PFQJHCPISA-N
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D-(+)-Ribonic -lactone
Empirical Formula (Hill Notation): C5H8O5 CAS Number: 5336-08-3 Molecular Weight: 148.11 Beilstein/REAXYS Number: 82057 EC Number: 226-256-5 MDL number: MFCD00063241 PubChem Substance ID: 24888436 NACRES: NA.22
Кат. номер 857297-5G 857297-1G 857297-100G ApplicationImportant building block for chiral acyclics, cyclopentenones, and oxabicyclic systems. Also employed in studies on nonlinear optical materials.Packaging5 g in glass bottleПараметрыQuality Level 200, assay 97% optical activity []24/D +18°, c = 1 in H2O mp 85-87 °C (lit.) SMILES string OC[C@H]1OC(=O)[C@H](O)[C@@H]1O InChI 1S/C5H8O5/c6-1-2-3(7)4(8)5(9)10-2/h2-4,6-8H,1H2/t2-,3-,4-/m1/s1 InChI key CUOKHACJLGPRHD-BXXZVTAOSA-N
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D-(+)-Sucrose octaacetate
Empirical Formula (Hill Notation): C28H38O19 CAS Number: 126-14-7 Molecular Weight: 678.59 Beilstein/REAXYS Number: 79290 EC Number: 204-772-1 MDL number: MFCD00006623 PubChem Substance ID: 24855224 NACRES: NA.22
Кат. номер 252603-1KG 252603-250G 252603-5G ApplicationLC-MS Analysis of Sucralose and Sucrose Octacetate on Ascentis RP-Amide
Sucrose octaacetate (SOA) is a bitter-tasting acetylated sugar that is commonly used to study gustatory sensitivity in mice.- SOA can undergo partial deacetylation by lipases or proteases to form analogs, which are useful intermediates for synthesizing artificial sweeteners.
- It can also be used as an in situ seed and a soft template to synthesize polyaniline (PANI) nanofibers under acidic conditions by the oxidative polymerization of aniline using ammonium peroxydisulfate (APS) as an oxidizing agent.
Packaging250 g in poly bottle
1 kg in poly bottleПараметрыQuality Level 200, assay 98% optical activity []22/D +58.8°, c = 2.5 in ethanol bp 260 °C (lit.) mp 82-85 °C (lit.) SMILES string CC(=O)OC[C@H]1O[C@H](O[C@]2(COC(C)=O)O[C@H](COC(C)=O)[C@@H](OC(C)=O)[C@@H]2OC(C)=O)[C@H](OC(C)=O)[C@@H](OC(C)=O)[C@@H]1OC(C)=O InChI 1S/C28H38O19/c1-12(29)37-9-20-22(40-15(4)32)24(42-17(6)34)25(43-18(7)35)27(45-20)47-28(11-39-14(3)31)26(44-19(8)36)23(41-16(5)33)21(46-28)10-38-13(2)30/h20-27H,9-11H2,1-8H3/t20-,21-,22-,23-,24+,25-,26+,27-,28+/m1/s1 InChI key ZIJKGAXBCRWEOL-SAXBRCJISA-N
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D-(+)-Talose
Empirical Formula (Hill Notation): C6H12O6 CAS Number: 2595-98-4 Molecular Weight: 180.16 Beilstein/REAXYS Number: 1724617 EC Number: 219-996-5 MDL number: MFCD00135834 PubChem Substance ID: 57653088 NACRES: NA.25
Кат. номер 86265-250MG 86265-1G ApplicationD-Talose, a C-2 epimer of galactose, is used as a substrate to identify, differentiate and characterize ribose-5-phosphate isomerase(s) of Clostridia.ПараметрыQuality Level 100, assay 99.0% (HPLC) optical activity []20/D +21±1°, 3 hr, c = 1% in H2O mp 124-127 °C solubility H2O: 0.1 g/mL SMILES string OC[C@H]1OC(O)[C@@H](O)[C@@H](O)[C@H]1O InChI 1S/C6H12O6/c7-1-2-3(8)4(9)5(10)6(11)12-2/h2-11H,1H2/t2-,3+,4+,5+,6?/m1/s1 InChI key WQZGKKKJIJFFOK-WHZQZERISA-N
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D-(+)-Trehalose dihydrate
Empirical Formula (Hill Notation): C12H22O11 · 2H2O CAS Number: 6138-23-4 Molecular Weight: 378.33 Beilstein/REAXYS Number: 5322018 EC Number: 202-739-6 MDL number: MFCD00071594 PubChem Substance ID: 24899871 NACRES: NA.75
Кат. номер T0167-10G-C T0167-100G T0167-5G T0167-25G T0167-EW T0167-10G General descriptionTrehalose is a non-reducing disaccharide, ubiquitously present in nature. It is used as a food preservative and also to retain enzymes, vaccines, cells and many other molecules. Trehalose is present as hemolymph sugar among the invertebrates.ApplicationD-(+)-Trehalose dihydrate has been used in a slow-freezing method for freezing rabbit oocytes. It has also been used in solid-surface vitrification (SSV) of in vitro-matured oocytes. It is suitable for use as a cryoprotectant in a variety of cell freezing media.Packaging10, 25, 100 g in poly bottleBiochem/physiol ActionsTrehalose is essential for embryogenesis, carbon metabolism, photosynthesis and flowering in plants. It predominantly exists among the species that supports anhydrobiosis (life without water). It serves as a carbohydrate reserve in microorganisms and protects them from adverse conditions, such as heat, cold, dehydration, desiccation and oxidation. Trehalose acts as a chemical chaperone affecting protein folding. It is known to prevent amyloid generation and accummulation of β-amyloid in vitro. A similar effect of trehalose has been observed with huntingtin protein aggregation. Thus, it might serve as a protective agent in Alzheimer′s disease and Huntington′s disease.ПараметрыQuality Level 200 biological source Saccharomyces cerevisiae product line BioReagent assay 99% form powder application(s) cell culture | insect: suitable, cell culture | mammalian: suitable solubility H2O: 50 mg/mL SMILES string [H]O[H].[H]O[H].OC[C@H]1O[C@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1O InChI 1S/C12H22O11.2H2O/c13-1-3-5(15)7(17)9(19)11(21-3)23-12-10(20)8(18)6(16)4(2-14)22-12;;/h3-20H,1-2H2;2*1H2/t3-,4-,5-,6-,7+,8+,9-,10-,11-,12-;;/m1../s1 InChI key DPVHGFAJLZWDOC-PVXXTIHASA-N
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