Lipids
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Agaric acid 1387-50MG
Empirical Formula (Hill Notation): C22H40O7 CAS Number: 666-99-9 Molecular Weight: 416.55 MDL number: MFCD00002665 Параметрыgrade analytical standard Quality Level 100, assay ≥95.0% (HPLC) shelf life limited shelf life, expiry date on the label impurities ≤8.0% water (calculated from elemental analysis) SMILES string CCCCCCCCCCCCCCCCC(C(O)=O)C(O)(CC(O)=O)C(O)=O InChI 1S/C22H40O7/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-18(20(25)26)22(29,21(27)28)17-19(23)24/h18,29H,2-17H2,1H3,(H,23,24)(H,25,26)(H,27,28) InChI key HZLCGUXUOFWCCN-UHFFFAOYSA-N
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all-cis-4,7,10,13,16,19-Docosahexaenoic acid methyl ester
Empirical Formula (Hill Notation): C23H34O2 CAS Number: 2566-90-7 Molecular Weight: 342.51 MDL number: MFCD00673450 PubChem Substance ID: 329748176 NACRES: NA.24
Кат. номер 5832-100MG 5832-VAR PackagingBottomless glass bottle. Contents are inside inserted fused cone.Параметрыgrade analytical standard Quality Level 100, assay ≥98.5% (GC) form liquid shelf life limited shelf life, expiry date on the label format neat functional group ester storage temp. −20°C SMILES string CC\C=C/C\C=C/C\C=C/C\C=C/C\C=C/C\C=C/CCC(=O)OC InChI 1S/C23H34O2/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22-23(24)25-2/h4-5,7-8,10-11,13-14,16-17,19-20H,3,6,9,12,15,18,21-22H2,1-2H3/b5-4-,8-7-,11-10-,14-13-,17-16-,20-19- InChI key VCDLWFYODNTQOT-JDPCYWKWSA-N
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Рапсовое масло с низким содержанием эруков AOCS Supelco O7756-1AMP
Общее описаниеNACRES: NA.24
Наши контрольные смеси животного и растительного происхождения соответствуют требованиям Американского общества нефтехимиков (AOCS) по методике Ce 1-62. Состав каждой смеси соответствует распределению жирных кислот в определенных маслах, указанных в каждом продукте. Пожалуйста, обратите внимание, что смеси AOCS, продаваемые под брендом Supelco, называются RM1, RM2 и т.д.
Приложение
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ПараметрыКласс аналитический стандарт Quality Level 100 Форма neat CofA текущий сертификат можно загрузить Упаковка ампула, содержащая 100 мг смеси метиловых эфиров жирных кислот, ампула, содержащая 100 мг Область применения ВЭЖХ: подходит, газовая хроматография (GC): подходит Формат neat shipped in dry ice Температура хранения −20°C
Информация по технике безопасностиRIDADR NONH for all modes of transport WGK Germany WGK 3 Flash Point F Непригодный Flash Point C Непригодный Узнать цену -
Arachidic acid
Empirical Formula (Hill Notation): C20H40O2 Linear Formula: CH3(CH2)18COOH CAS Number: 506-30-9 Molecular Weight: 312.53 Beilstein/REAXYS Number: 1788211 EC Number: 208-031-3 MDL number: MFCD00002755 PubChem Substance ID: 24890792 NACRES: NA.25
Кат. номер A3631-1G A3631-5G A3631-500MG A3631-25G A3631-10G ApplicationArachidic acid has been used as a fatty acid standard to optimize a sensitive high-performauce liquid chromatography (HPLC) method to analyse fatty acid (FA) for the quantification of polyunsaturated FAs (PUFAs) in cell lipid extracts.Packaging500 mg in poly bottle
1, 5, 10, 25 g in poly bottleBiochem/physiol ActionsArachidic acid is a saturated fatty acid with a 20 carbon chain. Arachidic acid occurs naturally in fish and vegetable oils. Diets rich in saturated fats like arachidic acid are associated with increased levels of serum low density lipoproteins.ПараметрыQuality Level 200, assay ≥99% form crystalline powder application(s) HPLC: suitable mp 74-76 °C (lit.) functional group carboxylic acid shipped in ambient storage temp. −20°C SMILES string CCCCCCCCCCCCCCCCCCCC(O)=O InChI 1S/C20H40O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20(21)22/h2-19H2,1H3,(H,21,22) InChI key VKOBVWXKNCXXDE-UHFFFAOYSA-N
Safety InformationPersonal Protective Equipment Eyeshields,, Gloves,, type N95 (US), RIDADR NONH for all modes of transport WGK Germany nwg Flash Point F 230.0 °F - closed cup Flash Point C 110 °C - closed cup Узнать цену -
Arachidonic acid
Empirical Formula (Hill Notation): C20H32O2 Linear Formula: CH3(CH2)4(CH=CHCH2)4CH2CH2CO2H CAS Number: 506-32-1 Molecular Weight: 304.47 Beilstein/REAXYS Number: 1713889 EC Number: 208-033-4 MDL number: MFCD00004417 PubChem Substance ID: 329770839 NACRES: NA.25
Кат. номер A3611-1G A3611-1G-PW A3611-100MG A3611-10MG-PW A3611-10MG A3611-100MG-PW Packaging10, 100 mg in ampule
1 g in ampule
Sealed ampuleBiochem/physiol ActionsArachidonic acid stimulates adhesion of MDA-MB-435 human metastatic cancer cells to extracellular matrix molecules (collagen IV and vitronectin) .
Arachidonic acid (AA) is an unsaturated 6 fatty acid constituent of the phospholipids of cell membranes. Phospholipase A2 releases AA from the membrane phospholipids in response to inflammation. AA is subsequently metabolized to prostaglandins and thromboxanes by at least two cyclooxygenase (COX) isoforms, to leukotrienes and lipoxins by lipoxygenases, and to epoxyeicosatrienoic acids via cytochrome p450-catalyzed metabolism. AA and its metabolites play important roles in a variety of biological processes, including signal transduction, smooth muscle contraction, chemotaxis, cell proliferation and differentiation, and apoptosis. AA has been demonstrated to bind to the a subunit of G protein and inhibit the activity of Ras GTPase-activating proteins (GAPs). Cellular uptake of AA is energy dependent and involves protein-facilitated transport across the plasma membrane.Параметрыbiological source non-animal source Quality Level 300, assay 98.5% (GC) form liquid refractive index n20/D 1.4872 (lit.) bp 169-171 °C/0.15 mmHg (lit.) mp 49 °C (lit.) density 0.922 g/mL at 25 °C (lit.) functional group carboxylic acid shipped in dry ice storage temp. 20°C SMILES string OC(CCC/C=C\C/C=C\C/C=C\C/C=C\CCCCC)=O InChI 1S/C20H32O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20(21)22/h6-7,9-10,12-13,15-16H,2-5,8,11,14,17-19H2,1H3,(H,21,22)/b7-6-,10-9-,13-12-,16-15- InChI key YZXBAPSDXZZRGB-DOFZRALJSA-N
Safety InformationRIDADR NONH for all modes of transport WGK Germany WGK 3 Flash Point F 235.4 °F - closed cup Flash Point C 113 °C - closed cup Узнать цену -
Brain Extract from bovine brain
NACRES: NA.25
Кат. номер B1502-CP B1502-1G B1502-25MG B1502-100MG General descriptionBrain extract has lipids, especially polyunsaturated fatty acids (PUFAs) at high level. Extract from substantia niagra and the striatum has high amount of iron.ApplicationBrain Extract from bovine brain has been used:- to prepare small unilamellar vesicles
- in lipid binding assay
- to aid the recovery of phosphoinositides and also to terminate the reaction in phosphatidylinositol 5-phosphate (PtdIns5P) and PtdIns4P assay
- in liposome and protein self-aggregation assays
Packaging25, 100 mg in ampule
1 g in ampule
Sealed ampule.Biochem/physiol ActionsBrain lipids are involved in cellular signal transduction, membrane organization, trafficking protein modification, interactions and energy storage.ComponentsContains phosphatidylinositol phosphatidylserine,other brain lipids.ПараметрыQuality Level 200, biological source bovine brain type Type I form powder storage temp. −20°C
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Brassicasterol B4936-5MG
Empirical Formula (Hill Notation): C28H46O CAS Number: 474-67-9 Molecular Weight: 398.66 EC Number: 207-486-5 MDL number: MFCD00201659 PubChem Substance ID: 329773247 NACRES: NA.77 ApplicationBrassicasterol was used as standard to analyze the sterols from mussels sample by thin layer chromatography.Packaging5 mg in glass bottleBiochem/physiol ActionsBrassicasterol is a plant sterol, structurally similar to cholesterol. Plant sterols compete with cholesterol and reduce the content of cholesterol incorporated into micelles thereby reducing its absorption. Brassicasterol reportedly decreases the progression of atherosclerosis. The level of brassicasterol in cerebrospinal fluid may be used as a prognostic factor for progression of Alzheimer′s disease.
Brassicasterol is a phytosterol found in rapeseed and canola oils; it is also present in marine algae and shellfish. Brassicasterol has been shown to inhibit sterol 24-reductase, an enzyme involved in the mammalian cholesterol biosynthesis pathway.Preparation NoteBrassicasterol is from a semi-synthetic source. It yields clear, colorless solution in chloroform at 50 mg/ml.Параметрыbiological source semisynthetic Quality Level 200, assay ≥98% (TLC) form powder shipped in wet ice storage temp. 2-8°C SMILES string CC(C)[C@@H](C)\C=C\[C@@H](C)[C@H]1CC[C@H]2[C@@H]3CC=C4C[C@@H](O)CC[C@]4(C)[C@H]3CC[C@]12C InChI 1S/C28H46O/c1-18(2)19(3)7-8-20(4)24-11-12-25-23-10-9-21-17-22(29)13-15-27(21,5)26(23)14-16-28(24,25)6/h7-9,18-20,22-26,29H,10-17H2,1-6H3/b8-7+/t19-,20+,22-,23-,24+,25-,26-,27-,28+/m0/s1 InChI key OILXMJHPFNGGTO-ZAUYPBDWSA-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 -
Campesterol
Empirical Formula (Hill Notation): C28H48O CAS Number: 474-62-4 Molecular Weight: 400.68 Beilstein/REAXYS Number: 3216975 EC Number: 207-484-4 MDL number: MFCD00010475 PubChem Substance ID: 24892762
Кат. номер C5157-10MG C5157-5MG C5157-1MG C5157-25MG ApplicationCampesterol was used as standard in GC and HPLC analysis of oil samples from plants.Packaging1, 5, 10 mg in glass bottleBiochem/physiol ActionsCampesterol is a phytosterol, primarily found in nuts, fruits, legumes and seeds. Though an analogue of cholesterol, it is poorly absorbed in humans and competitively inhibits the absorption of cholesterol. Campesterol decreases the transcription of genes involved in cholesterol metabolism in hepatocytes and enterocytes and has positive impact in treatment of cardiovascular disease.
Plant sterol. May lower absorption of dietary cholesterol.QualityAppears ~98% by HPLC and GC, but has been shown by 13C-NMR to contain ~35% dihydrobrassicasterol (24-methyl-5-cholesten-3-ol; 24[S]-ergost-5-en-3-ol).Preparation NoteCampesterol yields clear, colorless to faint yellow solution in chloroform at 20 mg/ml.Параметрыbiological source Glycine max (soybean) Quality Level 200, assay ~65% form powder shipped in ambient storage temp. 20°C SMILES string [H][C@@]12CC=C3C[C@@H](O)CC[C@]3(C)[C@@]1([H])CC[C@]4(C)[C@H](CC[C@@]24[H])[C@H](C)CC[C@H](C)C(C)C InChI 1S/C28H48O/c1-18(2)19(3)7-8-20(4)24-11-12-25-23-10-9-21-17-22(29)13-15-27(21,5)26(23)14-16-28(24,25)6/h9,18-20,22-26,29H,7-8,10-17H2,1-6H3/t19-,20+,22-,23-,24+,25-,26-,27-,28+/m0/s1 InChI key SGNBVLSWZMBQTH-ZRUUVFCLSA-N
Safety Informationpictograms GHS07 signalword Warning hcodes H302 + H312 + H332 - H315 - H319 - H335 pcodes P261 - P280 - P301 + P312 - P302 + P352 + P312 - P304 + P340 + P312 - P305 + P351 + P338 Target Organs Respiratory system Personal 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 -
Cardiolipin sodium salt from bovine heart
MDL number: MFCD00071040 NACRES: NA.25
Кат. номер C0563-100MG C0563-10MG C0563-25MG C0563-500MG C0563-PH C0563-10MG-PW C0563-25MG-PW C0563-500MG-PW C0563-100MG-PW General descriptionCardiolipin is localized in the inner membrane of mitochondria. It contains 18 carbon atoms, 3-phosphatidyl groups connected via a glycerol bridge. Cardiolipin is an important component of ATP synthase enzyme.ApplicationCardiolipin sodium salt from bovine heart has been used:- as a phospholipid standard in thin layer chromatography for the quantification of total mitochondrial lipids of Neurospora crassa(89)
- as an internal standard in reverse phase high performance liquid chromatography (RP-HPLC) for quantification of bacterial lipid extracts(90)
- as an antigen to evaluate IgM reaction in systemic lupus erythematosus (SLE) patients(91)
Biochem/physiol ActionsCardiolipin is a mitochondrial phospholipid that is found in mammalian tissues in low concentrations. It is often a membrane component. Inhibits cell attachment of fibronectin, vitronectin and Type I collagen.Packagingpackaged under argonПараметрыQuality Level 200, biological source bovine heart assay ≥97% (TLC) form lyophilized powder shipped in ambient storage temp. −20°C
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Cardiolipin solution from bovine heart
EC Number: 200-578-6 MDL number: MFCD00071040
Кат. номер SRE0029-500MG SRE0029-1000MG SRE0029-50MG SRE0029-250MG SRE0029-100MG Biochem/physiol ActionsCardiolipin is a mitochondrial phospholipid that is found in mammalian tissues in low concentrations. It is often a membrane component. Inhibits cell attachment of fibronectin, vitronectin and Type I collagen.Physical formApproximately 5 mg/ml in ethanol.Other Notes>80% polyunsaturated fatty acid content, primarily linoleic acid.ПараметрыQuality Level 400, biological source bovine heart assay ≥97% (TLC) form liquid concentration 4.7-5.3 mg/mL in ethanol shipped in wet ice storage temp. −20°C
Safety Informationpictograms GHS02,GHS07 signalword Danger hcodes H225 - H319 pcodes P210 - P305 + P351 + P338 RIDADR UN1170 - class 3 - PG 2 - Ethanol, solution WGK Germany WGK 2 Flash Point F 49.5 °F - closed cup - Solvent Flash Point C 9.7 °C - closed cup - Solvent Узнать цену -
Castor oil
CAS Number: 8001-79-4 EC Number: 232-293-8 MDL number: MFCD00130746 NACRES: NA.21
Кат. номер 259853-1L 259853-2.5L 259853-250ML 259853-5ML 259853-25ML ApplicationCastor oil is a triglyceride obtained from Ricinus communis. It has been used to study its impact on rat lens condition. Castor oil has also been used as a test reagent for studying the dose-response relationship and mechanism of action of Saccharomyces boulardii by utilizing the rat model of castor oil-induced diarrhea.Packaging1 L in glass bottle
250 mL in glass bottleПараметрыbiological source synthetic (organic) Quality Level 200, form liquid optical activity []20/D +5°, c = 5 in ethanol refractive index n20/D 1.478 (lit.) bp 313 °C (lit.) density 0.961 g/mL at 25 °C
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Ceramide from bovine spinal cord
MDL number: MFCD00146359 NACRES: NA.25
Кат. номер 22244-25MG 22244-100MG 22244-5G ApplicationCeramide is used to investigate effects on programmed cell death (apoptosis) and insulin signaling.Biochem/physiol ActionsCeramide is a minor component of cell membranes. Activates atypical protein kinase C (e.g., PKCzeta) .Preparation Notefrom cerebrosides by a modification of the procedure by H.E. Carter et al., J. Lipid Res. 2, 228 (1961)Other NotesSales restrictions may applyПараметрыbiological source bovine spinal cord Quality Level 100, assay ≥98.0% (TLC) form solid impurities α-hydroxy fatty acids solubility chloroform/methanol (99:1): 20 mg/mL, clear, colorless shipped in wet ice storage temp. −20°C
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Certified Reference Material Fatty Acid Methyl Ester (FAME) Standard CRMFAGO-250ML
CAS Number: 68334-30-5 EC Number: 269-822-7 NACRES: NA.24 General descriptionFatty Acid Methyl Ester (FAME) Certified Reference Material for the calibration and verification of laboratory instruments used for the determination of Fatty Acid Methyl Ester (FAME) content in middle distillates - Infrared spectrometry method, EN 14078Параметрыgrade certified reference material Quality Level 100, form liquid shelf life limited shelf life, expiry date on the label Торговая марка Paragon Scientific Ltd format matrix material storage temp. room temp
Safety Informationpictograms GHS02,GHS07,GHS08,GHS09 signalword Danger hcodes H226 - H304 - H315 - H332 - H351 - H373 - H411 pcodes P210 - P273 - P301 + P310 - P303 + P361 + P353 - P304 + P340 + P312 - P331 RIDADR UN1202 - class 3 - PG 3 - Diesel fuel WGK Germany WGK 2 Flash Point F 134.6 °F Flash Point C 57 °C Узнать цену -
Cholesta-3,5-diene
Empirical Formula (Hill Notation): C27H44 CAS Number: 747-90-0 Molecular Weight: 368.64 EC Number: 212-021-4 MDL number: MFCD00009939 PubChem Substance ID: 24892827 NACRES: NA.77
Кат. номер C6012-100MG C6012-25MG C6012-250MG C6012-5MG ApplicationCholesta-3,5-diene was used as standard in HPLC in quality analysis of different types of olive oils and edible fats.Packaging25, 100 mg in poly bottleBiochem/physiol ActionsCholesta-3,5-diene is an oxysterol, a cholesterol derivative by auto-oxidation. Oxysterols are non-genomic regulators of cholesterol homeostasis. The biological effects include protein prenylation, apoptosis, modulation of sphingolipid metabolism and platelet aggregation. Oxysterols bind to liver X receptors, modulate cholesterol efflux and decrease the uptake of cholesterol by the cells.Preparation NoteCholesta-3,5-diene yields clear, colorless solution in chloroform at 50 mg/ml.Параметрыbiological source natural (organic) Quality Level 200, assay ≥93% (HPLC) form powder mp 78-80 °C (lit.) shipped in ambient storage temp. −20°C SMILES string CC(C)CCC[C@@H](C)[C@H]1CC[C@H]2[C@@H]3CC=C4C=CCC[C@]4(C)[C@H]3CC[C@]12C InChI 1S/C27H44/c1-19(2)9-8-10-20(3)23-14-15-24-22-13-12-21-11-6-7-17-26(21,4)25(22)16-18-27(23,24)5/h6,11-12,19-20,22-25H,7-10,13-18H2,1-5H3/t20-,22+,23-,24+,25+,26+,27-/m1/s1 InChI key RLHIRZFWJBOHHD-HKQCOZBKSA-N
Safety Informationpictograms GHS07 signalword Warning hcodes H302 pcodes P264 - P270 - P301 + P312 - P501 Personal 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 -
Cholesterol
Empirical Formula (Hill Notation): C27H46O CAS Number: 57-88-5 Molecular Weight: 386.65 Beilstein/REAXYS Number: 1915888 EC Number: 200-353-2 MDL number: MFCD00003646 eCl@ss: 39023139 PubChem Substance ID: 24893094 NACRES: NA.77
Кат. номер C8667-100G C8667-1G C8667-5G C8667-500MG C8667-25G ApplicationStandard for chromatography
Cholesterol was used to prepare immune-stimulating complexes to enhance cellular and humoral responses. It was incorporated in animal feed to study the effect of cholesterol-rich diet.Packaging500 mg in poly bottle
1, 5, 25, 100 g in poly bottleBiochem/physiol ActionsCholesterol is a lipid that makes up about 20-25% of the structural components of the cell membranes. It determines the fluidity and permeability of the membrane, making it permeable to water but not to ions and protons. Cholesterol also regulates the functions of the transporters and signaling proteins present on the plasma membrane. The major sites of cholesterol synthesis are small intestine and liver.
Major component of all biological membranes; ~25% of total brain lipid is cholesterol.Preparation NoteCholesterol monohydrate yields a clear, colorless to faint yellow solution in hot alcohol. It is also soluble in acetone, dioxane, ethyl acetate, benzene, petroleum ether, oils, fats, and in aqueous solutions of bile salts. Solutions should be protected from light.ПараметрыQuality Level 200 biological source sheep wool grade Sigma Grade assay 99% form powder bp 360 °C (lit.) mp 147-149 °C (lit.) solubility water: soluble 0.00003 g/L at 20 °C density 1.067 g/mL at 25 °C (lit.) shipped in ambient storage temp. 20°C SMILES string CC(C)CCC[C@@H](C)[C@H]1CC[C@H]2[C@@H]3CC=C4C[C@@H](O)CC[C@]4(C)[C@H]3CC[C@]12C InChI 1S/C27H46O/c1-18(2)7-6-8-19(3)23-11-12-24-22-10-9-20-17-21(28)13-15-26(20,4)25(22)14-16-27(23,24)5/h9,18-19,21-25,28H,6-8,10-17H2,1-5H3/t19-,21+,22+,23-,24+,25+,26+,27-/m1/s1 InChI key HVYWMOMLDIMFJA-DPAQBDIFSA-N Gene Information human ... POLA1(5422), TOP2A(7153)
rat ... Ar(24208), Polb(29240)
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Cholesterol 5,6-epoxide
Empirical Formula (Hill Notation): C27H46O2 CAS Number: 1250-95-9 Molecular Weight: 402.65 EC Number: 215-007-6 MDL number: MFCD00046980 PubChem Substance ID: 24892526 NACRES: NA.77
Кат. номер C2773-50MG C2773-500MG C2773-100MG ApplicationCholesterol 5α, 6α-epoxide was incorporated in culture medium of human arterial endothelial cells to study oxysterol-induced toxicity.Packaging50 mg in glass bottleBiochem/physiol ActionsCholesterol 5α, 6α-epoxide is an oxysterol, a cholesterol derivative by auto-oxidation. Oxysterols are non-genomic regulators of cholesterol homeostasis. The biological effects include protein prenylation, apoptosis, modulation of sphingolipid metabolism and platelet aggregation. Oxysterols bind to liver X receptors, modulate cholesterol efflux and decrease the uptake of cholesterol by the cells.Preparation NoteCholesterol 5α, 6α-epoxide yields clear, colorless solution in chloroform at 50 mg/ml.Other NotesTandem Mass Spectrometry data independently generated by Scripps Center for Metabolomics is available to view or download in PDF. C2773.pdf, Tested metabolites are featured on Scripps Center for Metabolomics METLIN Metabolite Database. To learn more, visit sigma.com/metlin.,Параметрыassay ≥80% Quality Level 100, form powder functional group epoxy shipped in ambient storage temp. room temp SMILES string [H][C@@]12[C@]([C@](CC[C@H](O)C3)(C)[C@@]3(O4)[C@@H]4C2)([H])CC[C@@]5(C)[C@@]1([H])CC[C@]5([H])[C@]([H])(C)CCCC(C)C InChI 1S/C27H46O2/c1-17(2)7-6-8-18(3)21-9-10-22-20-15-24-27(29-24)16-19(28)11-14-26(27,5)23(20)12-13-25(21,22)4/h17-24,28H,6-16H2,1-5H3/t18-,19+,20+,21-,22+,23+,24+,25-,26-,27+/m1/s1 InChI key PRYIJAGAEJZDBO-ZEQHCUNVSA-N
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Cholesteryl arachidonate
Empirical Formula (Hill Notation): C47H76O2 CAS Number: 604-34-2 Molecular Weight: 673.11 MDL number: MFCD00056441 PubChem Substance ID: 24893099 NACRES: NA.77
Кат. номер C8753-10MG C8753-25MG C8753-100MG C8753-5MG C8753-500MG ApplicationCholesteryl arachidoante was oxidized and used to study the biological effects.Packaging10, 25 mg in glass bottleBiochem/physiol ActionsCholesteryl arachidonate is a cholesterol ester found associated with the neutral core of low density lipoprotein. Receptor-LDL complexes are taken up by lysosomes and hydrolyzed to release cholesterol from the esters. The enzyme acid cholesteryl ester hydrolase is responsible for the hydrolysis of cholesteryl esters; a defective enzyme can result in the formation of atherosclerotic lesions in humans.Preparation NoteCholesteryl arachidonate is a clear, colorless viscous liquid in chloroform.ПараметрыQuality Level 200, assay ≥95% (HPLC; detection at 205 nm) form viscous liquid color clear functional group ester shipped in dry ice storage temp. −20°C SMILES string CCCCC\C=C\C\C=C\C\C=C\C\C=C\CCCC(=O)OC1CCC2(C)C3CCC4(C)C(CCC4C3CC=C2C1)C(C)CCCC(C)C InChI 1S/C47H76O2/c1-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22-23-27-45(48)49-40-32-34-46(5)39(36-40)28-29-41-43-31-30-42(38(4)26-24-25-37(2)3)47(43,6)35-33-44(41)46/h11-12,14-15,17-18,20-21,28,37-38,40-44H,7-10,13,16,19,22-27,29-36H2,1-6H3/b12-11+,15-14+,18-17+,21-20+ InChI key IMXSFYNMSOULQS-SXXSVFILSA-N
Safety InformationPersonal Protective Equipment 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 -
Cholesteryl hemisuccinate tris salt
Empirical Formula (Hill Notation): C31H50O4 · C4H11NO3 CAS Number: 102601-49-0 Molecular Weight: 607.86 MDL number: MFCD00058298 eCl@ss: 39023139 PubChem Substance ID: 329775108 NACRES: NA.77
Кат. номер C6013-5G C6013-25G C6013-100G C6013-1G ApplicationCholesteryl hemisuccinate tris salt has been used:- to prepare solubilization buffer for glucan synthase assay
- to prepare immunoprecipitation buffer for immobilization of opioid receptors on paramagnetic beads.
- as a membrane stabilizer for liposomes and protein synaptogyrin-1
- as a component of a folate-modified self-microemulsifying drug delivery system.
- with N-dodecyl -D-maltoside (DDM) to solubilize erythrocyte ghosts and chemokine receptor CCR1
- for protein solubilization
Packaging5, 25 g in poly bottleBiochem/physiol ActionsCholesteryl hemisuccinate is an ionizable anionic detergent that stabilizes large unilamellar vesicles. These liposome vesicles act as delivery agents for anticancer drugs, oligonucleotides and antibiotics. Cholesteryl succinate also reportedly exhibits antiproliferative activity and may be clinically useful as antitumor agent.Preparation NoteCholesteryl hemisuccinate tris salt yields clear, colorless solution in methanol at 10 mg/ml.Параметрыbiological source synthetic (organic) Quality Level 200, assay ≥98% (TLC) form powder functional group ester shipped in ambient storage temp. −20°C SMILES string NC(CO)(CO)CO.CC(C)CCC[C@@H](C)[C@H]1CC[C@H]2[C@@H]3CC=C4C[C@H](CC[C@]4(C)[C@H]3CC[C@]12C)OC(=O)CCC(O)=O InChI 1S/C31H50O4.C4H11NO3/c1-20(2)7-6-8-21(3)25-11-12-26-24-10-9-22-19-23(35-29(34)14-13-28(32)33)15-17-30(22,4)27(24)16-18-31(25,26)5;5-4(1-6,2-7)3-8/h9,20-21,23-27H,6-8,10-19H2,1-5H3,(H,32,33);6-8H,1-3,5H2/t21-,23+,24+,25-,26+,27+,30+,31-;/m1./s1 InChI key SLDYONDUXRBLLR-XTCKSVDZSA-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 -
Cholesteryl linoleate
Empirical Formula (Hill Notation): C45H76O2 CAS Number: 604-33-1 Molecular Weight: 649.08 EC Number: 210-065-9 MDL number: MFCD00003644 PubChem Substance ID: 24892247 NACRES: NA.77
Кат. номер C0289-1G-PW C0289-1G C0289-100MG-PW C0289-PH C0289-250MG-PW C0289-100MG C0289-250MG C0289-500MG ApplicationCholesteryl linoleate was cosonicated with cholesterol to prepare dispersions were prepared to study the cholesterol to phospholipid ratio in red blood cell membrane. It was used as HPLC standard in the analysis of rat liver lipoproteins.Packaging100, 250 mg in ampule
1 g in ampule
Sealed ampuleBiochem/physiol ActionsCholesteryl linoleate is a major cholesterol ester found associated with the neutral core of low density lipoprotein. Receptor-LDL complexes are taken up by lysosomes and hydrolyzed to release cholesterol from the esters. The enzyme acid cholesteryl ester hydrolase is responsible for the hydrolysis of cholesteryl esters; a defective enzyme can result in the formation of atherosclerotic lesions in humans.
The most abundant cholesteryl ester in low density lipoprotein (LDL).Preparation NoteCholesteryl linoleate yields clear, colorless solution in chloroform at 100 mg/ml.Параметрыbiological source synthetic (organic) Quality Level 200, assay ≥98% (HPLC; detection at 205 nm) form powder functional group ester shipped in ambient storage temp. −20°C SMILES string CCCCC\C=C/C\C=C/CCCCCCCC(=O)O[C@H]1CC[C@]2(C)[C@H]3CC[C@]4(C)[C@H](CC[C@H]4[C@@H]3CC=C2C1)[C@H](C)CCCC(C)C InChI 1S/C45H76O2/c1-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-25-43(46)47-38-30-32-44(5)37(34-38)26-27-39-41-29-28-40(36(4)24-22-23-35(2)3)45(41,6)33-31-42(39)44/h11-12,14-15,26,35-36,38-42H,7-10,13,16-25,27-34H2,1-6H3/b12-11-,15-14-/t36-,38+,39+,40-,41+,42+,44+,45-/m1/s1 InChI key NAACPBBQTFFYQB-LJAITQKLSA-N
Safety InformationPersonal Protective Equipment Eyeshields,, Gloves,, type N95 (US), RIDADR NONH for all modes of transport WGK Germany WGK 3 Flash Point F Not applicable Flash Point C Not applicable Узнать цену -
Cholesteryl N-(2-dimethylaminoethyl)carbamate
Empirical Formula (Hill Notation): C32H56N2O2 CAS Number: 137056-72-5 Molecular Weight: 500.80 PubChem Substance ID: 329769879 NACRES: NA.85
Кат. номер 92243-500MG 92243-100MG Biochem/physiol ActionsCationic liposome, investigated in cancer gene therapy, as vaccine delivery system/adjuvant.PackagingBottomless glass bottle. Contents are inside inserted fused cone.ПараметрыQuality Level 100, assay 98% (TLC) form powder or crystals functional group ester storage temp. 20°C SMILES string CC(C)CCC[C@@H](C)[C@H]1CC[C@H]2[C@@H]3CC=C4CC(CC[C@]4(C)[C@H]3CC[C@]12C)OC(=O)NCCN(C)C InChI 1S/C32H56N2O2/c1-22(2)9-8-10-23(3)27-13-14-28-26-12-11-24-21-25(36-30(35)33-19-20-34(6)7)15-17-31(24,4)29(26)16-18-32(27,28)5/h11,22-23,25-29H,8-10,12-21H2,1-7H3,(H,33,35)/t23-,25?,26+,27-,28+,29+,31+,32-/m1/s1 InChI key HIHOWBSBBDRPDW-MTIZRNOUSA-N
Safety Informationhcodes H413 RIDADR NONH for all modes of transport WGK Germany WGK 3 Flash Point F Not applicable Flash Point C Not applicable Узнать цену -
Cholesteryl octanoate-1-13C 605905-1G
Empirical Formula (Hill Notation): 13CC34H60O2 Molecular Weight: 513.84 MDL number: MFCD01073406 PubChem Substance ID: 329759092 PackagingThis product may be available from bulk stock and can be packaged on demand. For information on pricing, availability and packaging, please contact Stable Isotopes Customer Service,.Параметрыisotopic purity 99 atom % 13C Quality Level 200, mp 110 °C mass shift M+1 SMILES string CCCCCCC[13C](=O)O[C@H]1CC[C@]2(C)C3CC[C@]4(C)[C@H](CCC4C3CC=C2C1)[C@H](C)CCCC(C)C InChI 1S/C35H60O2/c1-7-8-9-10-11-15-33(36)37-28-20-22-34(5)27(24-28)16-17-29-31-19-18-30(26(4)14-12-13-25(2)3)35(31,6)23-21-32(29)34/h16,25-26,28-32H,7-15,17-24H2,1-6H3/t26-,28+,29+,30-,31+,32+,34+,35-/m1/s1/i33+1 InChI key SKLBBRQPVZDTNM-SPKDLXGUSA-N
Safety InformationRIDADR NONH for all modes of transport WGK Germany 3 Узнать цену -
Cholesteryl oleate
Empirical Formula (Hill Notation): C45H78O2 CAS Number: 303-43-5 Molecular Weight: 651.10 Beilstein/REAXYS Number: 2343071 EC Number: 206-142-1 MDL number: MFCD00003645 PubChem Substance ID: 24893143 NACRES: NA.77
Кат. номер C9253-1G C9253-500MG C9253-250MG C9253-100MG ApplicationCholesteryl oleate was used to study the ability of silicone hydrogel contact lenses to absorb tear lipids, cholesterol and cholesterol esters. It was also used in the development of amperometric cholesterol biosensors.Packaging1 g in serum bottle
100, 250, 500 mg in serum bottleBiochem/physiol ActionsCholesterol in plasma is present in an esterified form such as Cholesteryl oleate. The liver is a primary source of cholesteryl oleate that enriches the LDL particles when released into plasma. The secretion of lipoproteins enriched with cholesteryl oleate has close correlation with the pathogenesis of coronary artery atherosclerosis.Preparation NoteCholesteryl oleate yields a clear, colorless solution in chloroform at 100 mg/ml.Параметрыbiological source synthetic (organic) Quality Level 200, assay ≥98% (HPLC; detection at 205 nm) form powder mp 44-47 °C (lit.) functional group ester shipped in ambient storage temp. −20°C SMILES string [H]\C(CCCCCCCC)=C(/[H])CCCCCCCC(=O)O[C@H]1CC[C@@]2(C)C(C1)=CC[C@]3([H])[C@]2([H])CC[C@]4(C)[C@]([H])(CC[C@@]34[H])[C@H](C)CCCC(C)C InChI 1S/C45H78O2/c1-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-25-43(46)47-38-30-32-44(5)37(34-38)26-27-39-41-29-28-40(36(4)24-22-23-35(2)3)45(41,6)33-31-42(39)44/h14-15,26,35-36,38-42H,7-13,16-25,27-34H2,1-6H3/b15-14-/t36-,38+,39+,40-,41+,42+,44+,45-/m1/s1 InChI key RJECHNNFRHZQKU-RMUVNZEASA-N
Safety InformationPersonal Protective Equipment Eyeshields,, Gloves,, type N95 (US), RIDADR NONH for all modes of transport WGK Germany WGK 3 Flash Point F Not applicable Flash Point C Not applicable Узнать цену -
Cholesteryl palmitate
Empirical Formula (Hill Notation): C43H76O2 CAS Number: 601-34-3 Molecular Weight: 625.06 Beilstein/REAXYS Number: 2342867 EC Number: 210-002-5 MDL number: MFCD00003638 PubChem Substance ID: 24892834 NACRES: NA.77
Кат. номер C6072-1G C6072-5G C6072-10G C6072-25G ApplicationCholesteryl palmitate was used as standard in HPLC analysis of lipids from cooked ground beef and rat liver and mouse muscle tissue samples.Packaging1 g in poly bottleBiochem/physiol ActionsCholesteryl palmitate was used as standard in HPLC analysis of lipids from cooked ground beef and rat liver and mouse muscle tissue samples.Параметрыbiological source synthetic (organic) Quality Level 200, assay ≥98% (HPLC; detection at 205 nm) form powder mp 74-77 °C (lit.) functional group ester shipped in ambient storage temp. −20°C SMILES string CCCCCCCCCCCCCCCC(=O)O[C@H]1CC[C@]2(C)C3CC[C@]4(C)C(CCC4C3CC=C2C1)[C@H](C)CCCC(C)C InChI 1S/C43H76O2/c1-7-8-9-10-11-12-13-14-15-16-17-18-19-23-41(44)45-36-28-30-42(5)35(32-36)24-25-37-39-27-26-38(34(4)22-20-21-33(2)3)43(39,6)31-29-40(37)42/h24,33-34,36-40H,7-23,25-32H2,1-6H3/t34-,36+,37+,38-,39+,40+,42+,43-/m1/s1 InChI key BBJQPKLGPMQWBU-JADYGXMDSA-N
Safety InformationPersonal Protective Equipment Eyeshields,, Gloves,, type N95 (US), RIDADR NONH for all modes of transport WGK Germany WGK 3 Flash Point F Not applicable Flash Point C Not applicable Узнать цену -
Cholesteryl phenylacetate
Empirical Formula (Hill Notation): C35H52O2 CAS Number: 33998-26-4 Molecular Weight: 504.79 EC Number: 251-781-1 MDL number: MFCD00021140 PubChem Substance ID: 24892533 NACRES: NA.77
Кат. номер C2800-25G C2800-1G C2800-5G Packaging25 g in poly bottleBiochem/physiol ActionsCholesteryl phenylacetate is a cholesterol ester found associated with the neutral core of low density lipoprotein. Receptor-LDL complexes are taken up by lysosomes and hydrolyzed to release cholesterol from the esters. The enzyme acid cholesteryl ester hydrolase is responsible for the hydrolysis of cholesteryl esters; a defective enzyme can result in the formation of atherosclerotic lesions in humans.Preparation NoteCholesteryl phenylacetate yields clear, colorless solution in chloroform at 50 mg/ml.Параметрыbiological source synthetic (organic) Quality Level 200, assay ≥98% (HPLC; detection at 258 nm) form crystalline powder functional group ester shipped in ambient storage temp. −20°C SMILES string O=C(O[C@@H]1CC2=CC[C@]3([H])[C@@](CC[C@@]4(C)[C@@]3([H])CC[C@]4([H])[C@H](C)CCCC(C)C)([H])[C@@]2(C)CC1)CC5=CC=CC=C5 InChI 1S/C35H52O2/c1-24(2)10-9-11-25(3)30-16-17-31-29-15-14-27-23-28(37-33(36)22-26-12-7-6-8-13-26)18-20-34(27,4)32(29)19-21-35(30,31)5/h6-8,12-14,24-25,28-32H,9-11,15-23H2,1-5H3/t25-,28?,29?,30?,31?,32?,34?,35?/m1/s1 InChI key JHFRODPXYCPTCM-ZTUKSAGPSA-N
Safety InformationPersonal Protective Equipment Eyeshields,, Gloves,, type N95 (US), RIDADR NONH for all modes of transport WGK Germany WGK 3 Flash Point F Not applicable Flash Point C Not applicable Узнать цену -
cis-10-Nonadecenoic acid N6394-250MG
Empirical Formula (Hill Notation): C19H36O2 CAS Number: 73033-09-7 Molecular Weight: 296.49 MDL number: MFCD00133177 PubChem Substance ID: 24897674 NACRES: NA.25 Packaging250 mg in ampule
Sealed ampule.Other NotesTandem Mass Spectrometry data independently generated by Scripps Center for Metabolomics is available to view or download in PDF. N6394.pdf, Tested metabolites are featured on Scripps Center for Metabolomics METLIN Metabolite Database. To learn more, visit sigma.com/metlin.,Параметрыbiological source synthetic (organic) Quality Level 200, assay 99% form liquid functional group carboxylic acid shipped in ambient storage temp. 20°C SMILES string CCCCCCCC\C=C/CCCCCCCCC(O)=O InChI 1S/C19H36O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19(20)21/h9-10H,2-8,11-18H2,1H3,(H,20,21)/b10-9- InChI key BBOWBNGUEWHNQZ-KTKRTIGZSA-N
Safety Informationpictograms GHS07 signalword Warning hcodes H315 - H319 - H335 pcodes P302 + P352 - P305 + P351 + P338 Target Organs Respiratory system Personal 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 -
cis-11-Eicosenoic acid
Empirical Formula (Hill Notation): C20H38O2 Linear Formula: CH3(CH2)7CH=CH(CH2)9CO2H CAS Number: 5561-99-9 Molecular Weight: 310.51 Beilstein/REAXYS Number: 1727313 MDL number: MFCD00010506 PubChem Substance ID: 329756557 NACRES: NA.24
Кат. номер 44878-VAR 44878-100MG 44878-500MG ApplicationRefer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.PackagingBottomless glass bottle. Contents are inside inserted fused cone.Other NotesTandem Mass Spectrometry data independently generated by Scripps Center for Metabolomics is available to view or download in PDF. 44878.pdf , Tested metabolites are featured on Scripps Center for Metabolomics METLIN Metabolite Database. To learn more, visit sigma.com/metlin.,ПараметрыQuality Level 100, biological source plant grade analytical standard assay 99.0% (GC) form neat shelf life limited shelf life, expiry date on the label application(s) HPLC: suitable, gas chromatography (GC): suitable refractive index n20/D 1.4606 (lit.) mp 23-24 °C (lit.) density 0.883 g/mL at 25 °C (lit.) format neat functional group carboxylic acid storage temp. 20°C SMILES string CCCCCCCC\C=C/CCCCCCCCCC(O)=O InChI 1S/C20H38O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20(21)22/h9-10H,2-8,11-19H2,1H3,(H,21,22)/b10-9- InChI key BITHHVVYSMSWAG-KTKRTIGZSA-N
Safety InformationPersonal Protective Equipment 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 -
cis-2-Decenoic acid 19699-25MG
Empirical Formula (Hill Notation): C10H18O2 CAS Number: 15790-91-7 Molecular Weight: 170.25 Beilstein/REAXYS Number: 1721990 MDL number: MFCD20543109 PubChem Substance ID: 329751935 NACRES: NA.25 Applicationcis-2-Decenoic acid may be used to study its cytotoxic effect on the human HepG2 cell line. It has also been used to study its synergistic anti-spirochetal effect.Biochem/physiol Actionscis-2-Decenoic acid is a fatty acid messenger (signaling molecule) produced by Pseudomonas aeruginosa. It possesses anti-biofilm property and converts most of the cells to planktonic (free-swimming) phenotype. cis-2-Decenoic acid retains the susceptibility of the bacteria towards antimicrobial agents. It does not exhibit any toxicity towards human cells and thus, might be used for treating biofilm-associated infections. cis-2-Decenoic acid is considered active even in nano-molar ranges. It mediates the transition of dormant P. aeruginosa and Escherichia coli to their biologically active state without affecting the number of cells. cis-2-Decenoic acid is effective against E. coli and Klebsiella pneumoniae mixed-species biofilms when used along with antimicrobial agents.PackagingBottomless glass bottle. Contents are inside inserted fused cone.ПараметрыQuality Level 100, assay 95.0% (HPLC), 95.0-105.0% (T) form liquid functional group carboxylic acid storage temp. 20°C SMILES string CCCCCCC\C=C/C(O)=O InChI 1S/C10H18O2/c1-2-3-4-5-6-7-8-9-10(11)12/h8-9H,2-7H2,1H3,(H,11,12)/b9-8- InChI key WXBXVVIUZANZAU-HJWRWDBZSA-N
Safety Informationpictograms GHS07 signalword Warning hcodes H315 - H319 - H412 pcodes P264 - P273 - P280 - P302 + P352 - P305 + P351 + P338 - P332 + P313 RIDADR NONH for all modes of transport WGK Germany WGK 1 Узнать цену -
cis-4,7,10,13,16,19-Docosahexaenoic acid
Empirical Formula (Hill Notation): C22H32O2 CAS Number: 6217-54-5 Molecular Weight: 328.49 Beilstein/REAXYS Number: 1715505 MDL number: MFCD00065722 PubChem Substance ID: 329757918 NACRES: NA.24
Кат. номер 53171-10MG 53171-VAR ApplicationRefer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.Параметрыgrade analytical standard Quality Level 100, assay 98.0% (GC) form neat shelf life limited shelf life, expiry date on the label application(s) HPLC: suitable, gas chromatography (GC): suitable format neat functional group carboxylic acid storage temp. 20°C SMILES string CC/C=C\C/C=C\C/C=C\C/C=C\C/C=C\C/C=C\CCC(O)=O InChI 1S/C22H32O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22(23)24/h3-4,6-7,9-10,12-13,15-16,18-19H,2,5,8,11,14,17,20-21H2,1H3,(H,23,24)/b4-3-,7-6-,10-9-,13-12-,16-15-,19-18- InChI key MBMBGCFOFBJSGT-KUBAVDMBSA-N
Safety InformationRIDADR NA 1993 / PGIII WGK Germany WGK 3 Flash Point F 143.6 °F - closed cup Flash Point C 62 °C - closed cup Узнать цену -
cis-4,7,10,13,16,19-Docosahexaenoic acid ethyl ester
Empirical Formula (Hill Notation): C24H36O2 CAS Number: 84494-72-4 Molecular Weight: 356.54 MDL number: MFCD00056293 PubChem Substance ID: 24893686 NACRES: NA.25
Кат. номер D2410-1G D2410-25MG D2410-100MG ПараметрыQuality Level 100, biological source algae assay 97% form liquid functional group ester shipped in ambient storage temp. 20°C SMILES string CCOC(=O)CC\C=C\C\C=C\C\C=C\C\C=C\C\C=C\C\C=C\CC InChI 1S/C24H36O2/c1-3-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22-23-24(25)26-4-2/h5-6,8-9,11-12,14-15,17-18,20-21H,3-4,7,10,13,16,19,22-23H2,1-2H3/b6-5+,9-8+,12-11+,15-14+,18-17+,21-20+ InChI key ITNKVODZACVXDS-YATCGRJWSA-N
Safety InformationPersonal Protective Equipment 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 -
cis-4,7,10,13,16,19-Docosahexaenoic acid methyl ester
Empirical Formula (Hill Notation): C23H34O2 Linear Formula: CH3(CH2CH=CH)6CH2CH2CO2CH3 CAS Number: 2566-90-7 Molecular Weight: 342.51 MDL number: MFCD00673450 PubChem Substance ID: 24893705 NACRES: NA.25
Кат. номер D2659-1G D2659-100MG D2659-PH D2659-50MG D2659-10MG Параметрыbiological source synthetic (organic) Quality Level 200, assay 98% form liquid refractive index n20/D 1.498 (lit.) density 0.921 g/mL at 25 °C (lit.) functional group ester shipped in ambient storage temp. 20°C SMILES string CC\C=C/C\C=C/C\C=C/C\C=C/C\C=C/C\C=C/CCC(=O)OC InChI 1S/C23H34O2/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22-23(24)25-2/h4-5,7-8,10-11,13-14,16-17,19-20H,3,6,9,12,15,18,21-22H2,1-2H3/b5-4-,8-7-,11-10-,14-13-,17-16-,20-19- InChI key VCDLWFYODNTQOT-JDPCYWKWSA-N
Safety InformationPersonal Protective Equipment Eyeshields,, Gloves,, multi-purpose combination respirator cartridge (US), RIDADR NONH for all modes of transport WGK Germany WGK 3 Flash Point F Not applicable Flash Point C Not applicable Узнать цену -
cis-5,8,11,14,17-Eicosapentaenoic acid
Empirical Formula (Hill Notation): C20H30O2 Linear Formula: CH3(CH2CH=CH)5(CH2)3CO2H CAS Number: 10417-94-4 Molecular Weight: 302.45 Beilstein/REAXYS Number: 1714433 MDL number: MFCD00065716 PubChem Substance ID: 329756555 NACRES: NA.24
Кат. номер 44864-VAR 44864-500MG 44864-100MG Applicationcis-5,8,11,14,17-Eicosapentaenoic acid has been used an analytical standard for the synthesis followed by investigation of pharmacological properties of aconitine-derived lipo-alkaloids.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.Biochem/physiol Actions5-Lipoxygenase inhibitor; reduces thromboxane A2 production.PackagingBottomless glass bottle. Contents are inside inserted fused cone.Параметрыbiological source fish oil Quality Level 100, grade analytical standard assay 98.5% (GC) form neat shelf life limited shelf life, expiry date on the label application(s) HPLC: suitable, gas chromatography (GC): suitable refractive index n20/D 1.4977 (lit.) mp 54-53 °C (lit.) density 0.943 g/mL at 25 °C (lit.) format neat functional group carboxylic acid storage temp. 20°C SMILES string CC/C=C\C/C=C\C/C=C\C/C=C\C/C=C\CCCC(O)=O InChI 1S/C20H30O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20(21)22/h3-4,6-7,9-10,12-13,15-16H,2,5,8,11,14,17-19H2,1H3,(H,21,22)/b4-3-,7-6-,10-9-,13-12-,16-15- InChI key JAZBEHYOTPTENJ-JLNKQSITSA-N
Safety InformationPersonal Protective Equipment Faceshields,, Gloves,, Goggles,, type ABEK (EN14387) respirator filter, RIDADR NONH for all modes of transport WGK Germany WGK 3 Flash Point F 200.1 °F - closed cup Flash Point C 93.4 °C - closed cup Узнать цену -
cis-7,10,13,16-Docosatetraenoic acid
Empirical Formula (Hill Notation): C22H36O2 CAS Number: 28874-58-0 Molecular Weight: 332.52 MDL number: MFCD00673435 PubChem Substance ID: 24893775 NACRES: NA.25
Кат. номер D3659-25MG D3659-100MG D3659-50MG Packaging25, 100 mg in ampule
Sealed ampuleПараметрыQuality Level 100, assay 98% (GC) form liquid functional group carboxylic acid shipped in ambient storage temp. 20°C SMILES string CCCCC\C=C/C\C=C/C\C=C/C\C=C/CCCCCC(O)=O InChI 1S/C22H36O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22(23)24/h6-7,9-10,12-13,15-16H,2-5,8,11,14,17-21H2,1H3,(H,23,24)/b7-6-,10-9-,13-12-,16-15- InChI key TWSWSIQAPQLDBP-DOFZRALJSA-N
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cis-7,10,13,16-Docosatetraenoic acid methyl ester
Empirical Formula (Hill Notation): C23H38O2 CAS Number: 13487-42-8 Molecular Weight: 346.55 MDL number: MFCD00673449 PubChem Substance ID: 24893767
Кат. номер D3534-25MG D3534-50MG D3534-100MG ПараметрыQuality Level 100, assay 98% (capillary GC) form liquid functional group ester shipped in ambient storage temp. 20°C SMILES string CCCCC\C=C/C\C=C/C\C=C/C\C=C/CCCCCC(=O)OC InChI 1S/C23H38O2/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22-23(24)25-2/h7-8,10-11,13-14,16-17H,3-6,9,12,15,18-22H2,1-2H3/b8-7-,11-10-,14-13-,17-16- InChI key ABGHYAFHPINIHF-ZKWNWVNESA-N
Safety InformationPersonal Protective Equipment Eyeshields,, Gloves,, multi-purpose combination respirator cartridge (US), RIDADR NONH for all modes of transport WGK Germany WGK 3 Flash Point F Not applicable Flash Point C Not applicable Узнать цену -
cis-8,11,14-Eicosatrienoic acid
Empirical Formula (Hill Notation): C20H34O2 Linear Formula: CH3(CH2)3(CH2CH=CH)3(CH2)6CO2H CAS Number: 1783-84-2 Molecular Weight: 306.48 Beilstein/REAXYS Number: 1796533 EC Number: 217-233-0 MDL number: MFCD00065721 PubChem Substance ID: 329761417 NACRES: NA.24
Кат. номер 69154-50MG 69154-VAR General descriptioncis-8,11,14-Eicosatrienoic acid is an unsaturated fatty acid, present in various plant species including Echium Rauwolfii, Sisymbrium Irio, Rhytididelphus squarrosus (Hedw.) Warnst etc, which are of pharmaceutical interest.Applicationcis-8,11,14-Eicosatrienoic acid may be used as an analytical reference standard for the determination of the analyte in plant species and biological matrices by chromatography-based techniques.Параметрыgrade analytical standard Quality Level 100, assay 98.5% (GC) form viscous liquid shelf life limited shelf life, expiry date on the label refractive index n20/D 1.478 (lit.) format neat functional group carboxylic acid storage temp. 20°C SMILES string CCCCC\C=C/C\C=C/C\C=C/CCCCCCC(O)=O InChI 1S/C20H34O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20(21)22/h6-7,9-10,12-13H,2-5,8,11,14-19H2,1H3,(H,21,22)/b7-6-,10-9-,13-12- InChI key HOBAELRKJCKHQD-QNEBEIHSSA-N
Safety InformationRIDADR NA 1993 / PGIII WGK Germany WGK 3 Flash Point F 143.6 °F - closed cup Flash Point C 62 °C - closed cup Узнать цену -
cis-Vaccenic acid
Empirical Formula (Hill Notation): C18H34O2 Linear Formula: CH3(CH2)5CH=CH(CH2)9CO2H CAS Number: 506-17-2 Molecular Weight: 282.46 Beilstein/REAXYS Number: 1726565 MDL number: MFCD00063187 PubChem Substance ID: 24900694 NACRES: NA.25
Кат. номер V0384-1G V0384-100MG Packaging100 mg in ampule
1 g in ampule
Sealed ampuleOther NotesTandem Mass Spectrometry data independently generated by Scripps Center for Metabolomics is available to view or download in PDF. V0384.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 Macadamia integrifolia oil assay 97% (capillary GC) form oil impurities <0.5% Trans-11 isomer refractive index n20/D 1.459 (lit.) bp 150 °C/0.03 mmHg (lit.) mp 14-15 °C (lit.) density 0.887 g/mL at 25 °C (lit.) functional group carboxylic acid shipped in ambient storage temp. 20°C SMILES string CCCCCC\C=C/CCCCCCCCCC(O)=O InChI 1S/C18H34O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18(19)20/h7-8H,2-6,9-17H2,1H3,(H,19,20)/b8-7- InChI key UWHZIFQPPBDJPM-FPLPWBNLSA-N
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cis/trans F.A.M.E Column Performance Mix 40495-U
EC Number: 200-838-9 NACRES: NA.24 ApplicationRefer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.ComponentsThis Fatty Acid Methyl Ester mix is composed of both cis and trans isomers for a variety of chain lengths.
Please note that the components and concentrations may vary from batch to batch.
Typical Composition:
C16:0
C18:0
C18:1 trans isomers
C18:1 cis and trans isomers
C18:1 cis isomers
C18:2
C20:0
C20:1
C18:3
C22:0Параметрыform liquid Quality Level 100, CofA current certificate can be downloaded packaging ampule of 1 mL concentration 2.5 mg/mL in dichloromethane application(s) HPLC: suitable, gas chromatography (GC): suitable format multi-component solution storage temp. 2-8°C
Safety Informationpictograms GHS07, GHS08 signalword Warning hcodes H315-H319-H336-H351 pcodes P201-P261-P264-P280-P304 + P340 + P312-P308 + P313 RIDADR UN 1593 6.1 / PGIII WGK Germany 2 Узнать цену -
Coconut oil from Cocos nucifera
CAS Number: 8001-31-8 EC Number: 232-282-8 MDL number: MFCD00130817 NACRES: NA.25
Кат. номер C1758-100G C1758-500G Packaging100, 500 g in glass bottlePhysical formUsually a solid at room temperatureПараметрыbiological source Cocos nucifera Quality Level 100, form low-melting solid mp 23-27 °C shipped in ambient storage temp. room temp
Safety InformationPersonal Protective Equipment Eyeshields,, Gloves,, type N95 (US), RIDADR NONH for all modes of transport WGK Germany WGK 1 Flash Point F 235.4 °F - closed cup Flash Point C > 113 °C - closed cup Узнать цену -
Cod liver oil fatty acid methyl esters
NACRES: NA.25
Кат. номер C5650-5G C5650-10G C5650-25G Other NotesNatural distribution of saturated and unsaturated fatty acids as methyl esters. Contains approx. 20% ω-3 (octadecatetraenoic, eicosapentaenoic and docosahexaenoic) methyl esters.Preparation NotePrepared by transmethylation of cod liver oil.Параметрыbiological source cod liver oil Quality Level 200, assay 15-25% (GC) form oil functional group ester shipped in ambient storage temp. 2-8°C
Safety InformationPersonal Protective Equipment Eyeshields,, Gloves,, multi-purpose combination respirator cartridge (US), RIDADR NONH for all modes of transport WGK Germany WGK 3 Flash Point F Not applicable Flash Point C Not applicable Узнать цену -
Coenzyme Q1
Empirical Formula (Hill Notation): C14H18O4 CAS Number: 727-81-1 Molecular Weight: 250.29 MDL number: MFCD00274412 PubChem Substance ID: 24892585 NACRES: NA.51
Кат. номер C7956-10MG C7956-5X10MG C7956-2MG Packaging2, 10 mg in glass bottleBiochem/physiol ActionsCoenzyme Q1 (CoQ1) is a 1 isoprenyl group (not naturally occurring) member of a family of ubiquinones that share a quinine chemical group but differ in the number of isoprenyl chemical subunits in their tail. The CoQ compounds are lipid soluble components of cell membranes where they perform multiple functions such as electron and proton transport. The most well studied CoQ compound is CoQ10. CoQ1 is frequently used in comparison studies on the effect of isoprenyl chain length on CoQ functions or distribution and to identify quinone reductases.Other NotesAnalog of coenzyme Q10 (not naturally occurring)
Tandem Mass Spectrometry data independently generated by Scripps Center for Metabolomics is available to view or download in PDF. C7956.pdf , Tested metabolites are featured on Scripps Center for Metabolomics METLIN Metabolite Database. To learn more, visit sigma.com/metlin.,ПараметрыQuality Level 100, assay 95% storage temp. 20°C SMILES string COC1=C(OC)C(=O)C(C\C=C(\C)C)=C(C)C1=O InChI 1S/C14H18O4/c1-8(2)6-7-10-9(3)11(15)13(17-4)14(18-5)12(10)16/h6H,7H2,1-5H3 InChI key SOECUQMRSRVZQQ-UHFFFAOYSA-N
Safety InformationPersonal Protective Equipment Eyeshields,, Gloves,, multi-purpose combination respirator cartridge (US), RIDADR NONH for all modes of transport WGK Germany WGK 3 Flash Point F Not applicable Flash Point C Not applicable Узнать цену -
Coenzyme Q4
Empirical Formula (Hill Notation): C29H42O4 CAS Number: 4370-62-1 Molecular Weight: 454.64 Beilstein/REAXYS Number: 2066531 MDL number: MFCD00077923 PubChem Substance ID: 24892492 NACRES: NA.51
Кат. номер C2470-5MG C2470-1MG ApplicationCoenzyme Q4 (CoQ4) is a 4 isoprenyl group member of a family of ubiquinones that share a quinine chemical group but differ in the number of isoprenyl chemical subunits in their tail. The CoQ compounds are lipid soluble components of cell membranes where they perform multiple functions such as electron and proton transport. The most well studied CoQ compound is CoQ10. CoQ4 is frequently used in comparison studies on the effect of isoprenyl chain length on CoQ functions or distribution.Packaging1, 5 mg in glass bottleBiochem/physiol ActionsIncreases the fluorescence polarization of perylene incorporated into ubiquinone-depleted mitochondrial and bilayer vesicles prepared from mitochondrial phospholipidsOther NotesTandem Mass Spectrometry data independently generated by Scripps Center for Metabolomics is available to view or download in PDF. C2470.pdf , Tested metabolites are featured on Scripps Center for Metabolomics METLIN Metabolite Database. To learn more, visit sigma.com/metlin.,Параметрыassay 90% storage temp. 20°C SMILES string COC1C(OC)C(=O)C(C\C=C(/C)CC\C=C(/C)CC\C=C(/C)CC\C=C(\C)C)=C(C)C1=O InChI 1S/C29H44O4/c1-20(2)12-9-13-21(3)14-10-15-22(4)16-11-17-23(5)18-19-25-24(6)26(30)28(32-7)29(33-8)27(25)31/h12,14,16,18,28-29H,9-11,13,15,17,19H2,1-8H3/b21-14+,22-16+,23-18+ InChI key MDLQEORKYVBTDV-INVBOZNNSA-N
Safety InformationPersonal Protective Equipment 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 -
Conjugated (9E,11E)-Linoleic acid
Empirical Formula (Hill Notation): C18H32O2 CAS Number: 544-71-8 Molecular Weight: 280.45 MDL number: MFCD00133681 PubChem Substance ID: 329769982 NACRES: NA.24
Кат. номер 90983-20MG 90983-VAR General descriptionConjugated (9E,11E)-linoleic acid can be obtained via hydrogenation of linoleic acid in the middle [12,13] double bond.ApplicationRefer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.PackagingBottomless glass bottle. Contents are inside inserted fused cone.ПараметрыQuality Level 100, biological source synthetic grade analytical standard assay ≥98.0% (HPLC) form neat shelf life limited shelf life, expiry date on the label application(s) HPLC: suitable, gas chromatography (GC): suitable format neat functional group carboxylic acid storage temp. −20°C SMILES string CCCCCC\C=C\C=C\CCCCCCCC(O)=O InChI 1S/C18H32O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18(19)20/h7-10H,2-6,11-17H2,1H3,(H,19,20)/b8-7+,10-9+ InChI key JBYXPOFIGCOSSB-XBLVEGMJSA-N
Safety InformationPersonal Protective Equipment 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 -
Conjugated (9Z,11E)-Linoleic acid
Empirical Formula (Hill Notation): C18H32O2 CAS Number: 2540-56-9 Molecular Weight: 280.45 MDL number: MFCD00211047 PubChem Substance ID: 329751210 NACRES: NA.24
Кат. номер 16413-50MG 16413-VAR General descriptionConjugated Linoleic acid is a naturally occurring fatty acid. It has anti-cancer, anti-atherogenic and anti-diabetic properties. 9Z,11E is a geometric isomer which belongs to linoleate group.ApplicationIt was may be used for HPLC-ESI-MS/MS analysis to quantify and also structural analysis of nitrated species of CLA.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.PackagingBottomless glass bottle. Contents are inside inserted fused cone.ПараметрыQuality Level 100, biological source synthetic grade analytical standard assay 96.0% (HPLC) form neat application(s) HPLC: suitable, gas chromatography (GC): suitable refractive index n20/D 1.478-1.483 format neat functional group carboxylic acid storage temp. 20°C SMILES string CCCCCC\C=C\C=C/CCCCCCCC(O)=O InChI 1S/C18H32O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18(19)20/h7-10H,2-6,11-17H2,1H3,(H,19,20)/b8-7+,10-9- InChI key JBYXPOFIGCOSSB-GOJKSUSPSA-N
Safety InformationPersonal Protective Equipment 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 -
Corn oil
CAS Number: 8001-30-7 EC Number: 232-281-2 MDL number: MFCD00130865 NACRES: NA.25
Кат. номер C8267-500ML C8267-2.5L General descriptionCorn oil is used as a delivery vehicle for lipophilic substances and is available in pharmaceutical and nonpharmaceutical grade. It has high polyunsaturated lipid content than the saturated lipids.ApplicationCorn oil has been used in research applications as delivery vehicle for fat-soluble compounds including toxins. It is also used in the delivery of tamoxifen (TAM) in mice, curcumin in rats and [3H]retinol in mice.
corn oil has been used in research applications as delivery vehicle for fat-soluble compounds including toxins.Packaging500 mL in poly bottle
2.5 L in poly bottleПараметрыQuality Level 100 biological source maize form liquid density 0.9 g/mL at 25 °C (lit.) functional group ester shipped in ambient storage temp. room temp
Safety InformationPersonal Protective Equipment Eyeshields, Gloves RIDADR NONH for all modes of transport WGK Germany awg Flash Point(F) 489.2 °F - open cup Flash Point(C) 254 °C - open cup Узнать цену -
Corticosterone
Empirical Formula (Hill Notation): C21H30O4 CAS Number: 50-22-6 Molecular Weight: 346.46 Beilstein/REAXYS Number: 2339601 EC Number: 200-019-6 MDL number: MFCD00037715 PubChem Substance ID: 57648276 NACRES: NA.77
Кат. номер 27840-100MG 27840-500MG General descriptionCorticosterone (Cort) is a glucocorticoid hormone. It is also the principal hormone that mediates stress responses in birds. It is the primary adrenal cortical steroid in rat plasma. The influence of maternal Cort exposure on the developing placenta has been studied in a mouse model.ApplicationCorticosterone was used to study the adrenoceptor signaling in rats, lizards or in vitro. It was also used in immune suppression experiment.Biochem/physiol ActionsCorticosterone is synthesized from cholesterol in the adrenal cortex that activates both mineralocorticoid and glucocorticoid receptors. The role of corticosterones is vital for reproductive processes including ovulation, lutenization, development of oocytes, parturition and lactation. The metabolism of corticosterone is modulated by the enzyme 11β-hydroxysteroid dehydrogenase.PackagingBottomless glass bottle. Contents are inside inserted fused cone.Preparation NoteCorticosterone is soluble in chloroform and ethanol.ПараметрыQuality Level 200, biological source synthetic assay 98.5% (HPLC) form powder or crystals optical activity []20/D +223±3°, c = 1% in ethanol mp 179-183 °C (lit.), 179-183 °C functional group ketone SMILES string C[C@]12C[C@H](O)[C@H]3[C@@H](CCC4=CC(=O)CC[C@]34C)[C@@H]1CC[C@@H]2C(=O)CO InChI 1S/C21H30O4/c1-20-8-7-13(23)9-12(20)3-4-14-15-5-6-16(18(25)11-22)21(15,2)10-17(24)19(14)20/h9,14-17,19,22,24H,3-8,10-11H2,1-2H3/t14-,15-,16+,17-,19+,20-,21-/m0/s1 InChI key OMFXVFTZEKFJBZ-HJTSIMOOSA-N Gene Information human ... EBP(10682), SERPINA6(866)
rat ... Ar(24208), Nr3c1(24413)
Safety InformationPersonal Protective Equipment dust mask type N95 (US),, Eyeshields,, Faceshields,, Gloves, RIDADR NONH for all modes of transport WGK Germany WGK 3 Узнать цену -
Cottonseed oil 47113
CAS Number: 8001-29-4 EC Number: 232-280-7 MDL number: MFCD00130872 General descriptionCottonseed oil is a vegetable oil, which is derived mainly from the seeds of Gossypium hirsutum or Gossypium barbadense. It is commonly used as a food and cooking oil.ApplicationRefer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.Параметрыgrade analytical standard Quality Level 100, form neat CofA current certificate can be downloaded packaging ampule of 1000 mg application(s) HPLC: suitable, gas chromatography (GC): suitable format neat storage temp. room temp
Safety InformationPersonal Protective Equipment Eyeshields,, Gloves, RIDADR NONH for all modes of transport WGK Germany awg Flash Point F Not applicable Flash Point C Not applicable Узнать цену -
Cottonseed oil
CAS Number: 8001-29-4 EC Number: 232-280-7 MDL number: MFCD00130872 NACRES: NA.25
Кат. номер C7767-500ML C7767-1L General descriptionCottonseed oil is extracted from the seeds of Gossypium sp. It is used to impart a roasted or nutty aroma to fried food products. Cottonseed oil is used as a component to formulate shortenings and margarines. It has a long shelf life and is healthy for the heart.
Cottonseed oil is extracted from the kernel, a part of the cotton seed. This oil contains linoleic acid, oleic acid, linolenic acid and myristic acid. It is used as non-edible oil and is used in the preparation of polymeric resins.ApplicationCottonseed oil has been used as an nutritional supplement for alveolar septal wall thickness in mice. It has been used to study its effects on indirect gestational and lactational exposure in rats.
Cottonseed oil has been used to dissolve testosterone propionate employed in preparation of prenatal testosterone -treated Suffolk ewes.Packaging500 mL in poly bottle
1 L in poly bottleПараметрыbiological source plant (Gossypium hirsutum L.) Quality Level 100, form liquid composition unsaturated fatty acids, ~70% density 0.92 g/mL at 25 °C (lit.) shipped in ambient storage temp. room temp
Safety InformationPersonal Protective Equipment Eyeshields,, Gloves, RIDADR NONH for all modes of transport WGK Germany nwg Flash Point F Not applicable Flash Point C Not applicable Узнать цену -
Croton oil
CAS Number: 8001-28-3 MDL number: MFCD00130880 NACRES: NA.25
Кат. номер C6719-10G C6719-25G C6719-100G General descriptionCroton oil is a toxic viscous liquid extracted from seeds of Croton tiglium. It is pale yellow to brown in color and is transparent in nature. Croton oil has a strong irritant property and is used along with phenol in some chemical peels. It also has a tumor promoting ability.
Croton oil is extracted from Croton tiglium L. It consists of crotonoleic acid, crotonic acid, crotonyl alcohol, crotonyl alcohol bisester and crotonyl alcohol trisester. Croton oil acts as a stimulant in the skin and mucosal inflammation. It is associated with allergic contact dermatitis (ACD) and skin carcinoma. Croton oil functions as a skin peeling agent.ApplicationCroton oil has been used to induce acute skin inflammation.
Croton oil has been used to induce inflammation in mouse ears.Packaging10, 25, 100 g in glass bottleOther NotesEssential oil rich in glycerides of saturated fatty acids, and in phorbol esters.Параметрыbiological source plant (Croton tiglium L) Quality Level 100, form viscous liquid density 0.94 g/mL at 25 °C (lit.) functional group ester shipped in ambient storage temp. room temp
Safety InformationPersonal Protective Equipment Eyeshields,, Gloves,, multi-purpose combination respirator cartridge (US), RIDADR NONH for all modes of transport WGK Germany WGK 3 Flash Point F 165.2 °F - closed cup Flash Point C 74 °C - closed cup Узнать цену -
D--Phosphatidylcholine, dipalmitoyl
PubChem Substance ID: 24898230 NACRES: NA.25
Кат. номер P1652-500MG P1652-100MG P1652-25MG Packaging500 mg in poly bottleOther NotesThis is the stereoisomer of phosphatidylcholine which is inactive as a substrate for snake venom phospholipase A2.Параметрыbiological source semisynthetic Quality Level 200, assay 99% form powder functional group phospholipid shipped in ambient storage temp. 20°C
Safety InformationPersonal Protective Equipment Eyeshields,, Gloves,, type N95 (US), RIDADR NONH for all modes of transport WGK Germany WGK 3 Flash Point F Not applicable Flash Point C Not applicable Узнать цену
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