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L--Homophenylalanine hydrochloride
Empirical Formula (Hill Notation): C10H13NO2 · HCl CAS Number: 138165-77-2 Molecular Weight: 215.68 Beilstein/REAXYS Number: 8083915 MDL number: MFCD01862875 PubChem Substance ID: 329747806 NACRES: NA.22
Кат. номер 3769-VAR 3769-250MG 3769-1G ПараметрыQuality Level 100, assay 98.0% form powder reaction suitability reaction type: solution phase peptide synthesis application(s) peptide synthesis: suitable color white to faint beige SMILES string Cl.N[C@H](CC(O)=O)Cc1ccccc1 InChI 1S/C10H13NO2.ClH/c11-9(7-10(12)13)6-8-4-2-1-3-5-8;/h1-5,9H,6-7,11H2,(H,12,13);1H/t9-;/m0./s1 InChI key MQTMGKGSJOPWJW-FVGYRXGTSA-N
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L--Homoproline hydrochloride
Empirical Formula (Hill Notation): C6H11NO2 · HCl CAS Number: 53912-85-9 Molecular Weight: 165.62 Beilstein/REAXYS Number: 471672 MDL number: MFCD07363484 PubChem Substance ID: 329747805 NACRES: NA.26
Кат. номер 3768-VAR 3768-250MG 3768-1G ApplicationL-β-homoproline is a non-coded α-imino acid used in organic peptide synthesis.Biochem/physiol ActionsL-β-Homoproline is a β amino acid useful in peptide and protein conformation studies.ПараметрыQuality Level 100, assay 98.0% (TLC) form powder application(s) peptide synthesis: suitable color white to light brown SMILES string Cl.OC(=O)C[C@@H]1CCCN1 InChI 1S/C6H11NO2.ClH/c8-6(9)4-5-2-1-3-7-5;/h5,7H,1-4H2,(H,8,9);1H/t5-;/m0./s1 InChI key VQDACVOAOJQTPR-JEDNCBNOSA-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 -
L--Homoserine
Empirical Formula (Hill Notation): C4H9NO3 CAS Number: 16504-56-6 Molecular Weight: 119.12 Beilstein/REAXYS Number: 7770197 MDL number: MFCD00270242 eCl@ss: 32160406 PubChem Substance ID: 329747775 NACRES: NA.22
Кат. номер 3694-VAR 3694-100MG 3694-500MG ПараметрыQuality Level 100, assay 98.0% (TLC) form powder or crystals reaction suitability reaction type: solution phase peptide synthesis application(s) peptide synthesis: suitable color white to off-white SMILES string N[C@@H](CO)CC(O)=O InChI 1S/C4H9NO3/c5-3(2-6)1-4(7)8/h3,6H,1-2,5H2,(H,7,8)/t3-/m1/s1 InChI key BUZICZZQJDLXJN-GSVOUGTGSA-N
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L--Homothreonine
Empirical Formula (Hill Notation): C5H11NO3 CAS Number: 192003-00-2 Molecular Weight: 133.15 MDL number: MFCD10567448 PubChem Substance ID: 329747804 NACRES: NA.22
Кат. номер 3767-VAR 3767-100MG 3767-500MG ПараметрыQuality Level 100, assay 98.0% (TLC) form powder reaction suitability reaction type: solution phase peptide synthesis application(s) peptide synthesis: suitable color colorless to white SMILES string C[C@@H](O)[C@H](N)CC(O)=O InChI 1S/C5H11NO3/c1-3(7)4(6)2-5(8)9/h3-4,7H,2,6H2,1H3,(H,8,9)/t3-,4-/m1/s1 InChI key NIVRJEWVLMOZNV-QWWZWVQMSA-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 -
L--Leucine hydrochloride
Empirical Formula (Hill Notation): C6H13NO2 · HCl CAS Number: 219310-09-5 Molecular Weight: 167.63 Beilstein/REAXYS Number: 6781440 MDL number: MFCD01862852 PubChem Substance ID: 329747764 NACRES: NA.22
Кат. номер 3675-VAR 3675-1G 3675-250MG ПараметрыQuality Level 100, assay 98.0% form powder reaction suitability reaction type: solution phase peptide synthesis application(s) peptide synthesis: suitable color white to off-white SMILES string Cl.CC(C)[C@H](N)CC(O)=O InChI 1S/C6H13NO2.ClH/c1-4(2)5(7)3-6(8)9;/h4-5H,3,7H2,1-2H3,(H,8,9);1H/t5-;/m1./s1 InChI key SLNFFBWDHRKWCB-NUBCRITNSA-N
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L-2-Amino-3-guanidinopropionic acid hydrochloride
Empirical Formula (Hill Notation): C4H10N4O2 · HCl CAS Number: 1482-99-1 Molecular Weight: 182.61 Beilstein/REAXYS Number: 6317820 EC Number: 216-044-0 MDL number: MFCD00036989 PubChem Substance ID: 24890971 NACRES: NA.26
Кат. номер A5402-100MG A5402-500MG Параметрыassay 97.5% (TLC) Quality Level 200, form powder application(s) peptide synthesis: suitable color white storage temp. 2-8°C SMILES string Cl[H].N[C@@H](CNC(N)=N)C(O)=O InChI 1S/C4H10N4O2.ClH/c5-2(3(9)10)1-8-4(6)7;/h2H,1,5H2,(H,9,10)(H4,6,7,8);1H/t2-;/m0./s1 InChI key ZOXYHKHLLCDEAX-DKWTVANSSA-N
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L-2-Aminobutyric acid
Empirical Formula (Hill Notation): C4H9NO2 CAS Number: 1492-24-6 Molecular Weight: 103.12 Beilstein/REAXYS Number: 1720935 EC Number: 216-083-3 MDL number: MFCD00064415 PubChem Substance ID: 24890595
Кат. номер A1879-5G A1879-1G 2530015 A1879-250MG Packaging1, 5 g in glass bottleOther NotesTandem Mass Spectrometry data independently generated by Scripps Center for Metabolomics is available to view or download in PDF. A1879.pdf , Tested metabolites are featured on Scripps Center for Metabolomics METLIN Metabolite Database. To learn more, visit sigma.com/metlin.,ПараметрыQuality Level 400,, 200, assay 99% (titration) form powder application(s) ligand binding assay: suitable, peptide synthesis: suitable color white SMILES string CC[C@H](N)C(O)=O InChI 1S/C4H9NO2/c1-2-3(5)4(6)7/h3H,2,5H2,1H3,(H,6,7)/t3-/m0/s1 InChI key QWCKQJZIFLGMSD-VKHMYHEASA-N
Safety Informationpictograms GHS07 signalword Warning hcodes H317 pcodes P280 Personal Protective Equipment dust mask type N95 (US),, Eyeshields,, Faceshields,, Gloves, RIDADR NONH for all modes of transport WGK Germany WGK 3 Flash Point F Not applicable Flash Point C Not applicable Узнать цену -
L-4-Thiazolidinecarboxylic acid
Empirical Formula (Hill Notation): C4H7NO2S CAS Number: 34592-47-7 Molecular Weight: 133.17 Beilstein/REAXYS Number: 81065 EC Number: 252-106-3 MDL number: MFCD00005212 PubChem Substance ID: 24900069 NACRES: NA.22
Кат. номер T27502-10G T27502-100G ApplicationUsed in peptide coupling reactions.Packaging10, 100 g in poly bottleПараметрыQuality Level 200, assay 98% form powder optical activity []20/D 141°, c = 1.3 in H2O reaction suitability reaction type: solution phase peptide synthesis color white mp 190-200 °C (dec.) (lit.) SMILES string OC(=O)[C@@H]1CSCN1 InChI 1S/C4H7NO2S/c6-4(7)3-1-8-2-5-3/h3,5H,1-2H2,(H,6,7)/t3-/m0/s1 InChI key DZLNHFMRPBPULJ-VKHMYHEASA-N
Safety Informationpictograms GHS06 signalword Danger hcodes H301 - H312 + H332 - H315 - H319 - H335 pcodes P261 - P280 - P301 + P310 - P302 + P352 + P312 - P304 + P340 + P312 - P305 + P351 + P338 Target Organs Respiratory system Personal Protective Equipment dust mask type N95 (US),, Eyeshields,, Faceshields,, Gloves, RIDADR UN 2811 6.1 / PGIII WGK Germany WGK 3 Flash Point F Not applicable Flash Point C Not applicable Узнать цену -
L-Alanine
Empirical Formula (Hill Notation): C3H7NO2 CAS Number: 56-41-7 Molecular Weight: 89.09 Beilstein/REAXYS Number: 1720248 EC Number: 200-273-8 MDL number: MFCD00064410 eCl@ss: 32160406 PubChem Substance ID: 24891260 NACRES: NA.26
Кат. номер A7627-1G-KC A7627-500G A7627-100G A7627-1G A7627-1KG A7627-25G A7627-5KG A7627-5G General descriptionL-Alanine, a non-essential amino acid, is produced enzymatically from L-aspartate using aspartate -decarboxylase. It is the smallest among all the aminoacids.ApplicationL-Alanine has been used as a supplement in complete medium for cell culture.Packaging1, 100, 500 g in poly bottle
1 kg in poly bottleПараметрыQuality Level 100, assay 98% (TLC) form powder application(s) cell culture | mammalian: suitable, peptide synthesis: suitable color white solubility H2O: 50 mg/mL, clear, colorless SMILES string C[C@H](N)C(O)=O InChI 1S/C3H7NO2/c1-2(4)3(5)6/h2H,4H2,1H3,(H,5,6)/t2-/m0/s1 InChI key QNAYBMKLOCPYGJ-REOHCLBHSA-N Gene Information human ... CA1(759), CA2(760)
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L-Alanine benzyl ester p-toluenesulfonate salt
Empirical Formula (Hill Notation): C10H13NO2 · C7H8O3S Linear Formula: CH3CH(NH2)COOCH2C6H5 · HOSO2C6H4CH3 CAS Number: 42854-62-6 Molecular Weight: 351.42 Beilstein/REAXYS Number: 3586474 EC Number: 255-969-4 MDL number: MFCD00066143 PubChem Substance ID: 329747655 NACRES: NA.22
Кат. номер 5183-VAR 5183-5G 5183-1G ПараметрыQuality Level 100, assay 95.0% (T) form powder optical activity []20/D 5.0±0.5°, c = 3% in methanol reaction suitability reaction type: solution phase peptide synthesis application(s) peptide synthesis: suitable color colorless to white mp 112-116 °C SMILES string Cc1ccc(cc1)S(O)(=O)=O.C[C@H](N)C(=O)OCc2ccccc2 InChI 1S/C10H13NO2.C7H8O3S/c1-8(11)10(12)13-7-9-5-3-2-4-6-9;1-6-2-4-7(5-3-6)11(8,9)10/h2-6,8H,7,11H2,1H3;2-5H,1H3,(H,8,9,10)/t8-;/m0./s1 InChI key NWOPHJSSBMABBD-QRPNPIFTSA-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 -
L-Alanine tert-butyl ester hydrochloride
Empirical Formula (Hill Notation): C7H15NO2 · HCl Linear Formula: CH3CH(NH2)COOC(CH3)3 · HCl CAS Number: 13404-22-3 Molecular Weight: 181.66 Beilstein/REAXYS Number: 3562140 EC Number: 236-497-8 MDL number: MFCD00035524 PubChem Substance ID: 329747657 NACRES: NA.22
Кат. номер 5190-VAR 5190-5G 5190-1G ПараметрыQuality Level 100, assay 99.0% (AT) form powder optical activity []20/D +1.4±0.2°, c = 2% in ethanol reaction suitability reaction type: solution phase peptide synthesis application(s) peptide synthesis: suitable color white to off-white mp 168-175 °C storage temp. 2-8°C SMILES string Cl.C[C@H](N)C(=O)OC(C)(C)C InChI 1S/C7H15NO2.ClH/c1-5(8)6(9)10-7(2,3)4;/h5H,8H2,1-4H3;1H/t5-;/m0./s1 InChI key WIQIWPPQGWGVHD-JEDNCBNOSA-N
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L-allo-Isoleucine
Empirical Formula (Hill Notation): C6H13NO2 CAS Number: 1509-34-8 Molecular Weight: 131.17 Beilstein/REAXYS Number: 1721791 EC Number: 216-142-3 MDL number: MFCD00066446 eCl@ss: 32160406 PubChem Substance ID: 24896143
Кат. номер I8754-100MG I8754-1G I8754-25MG Biochem/physiol ActionsL-allo-Isoleucine may be used in studies on maple syrup urine disease.Параметрыassay 99% Quality Level 200, form powder color white to off-white mp 285 °C SMILES string CC[C@@H](C)[C@H](N)C(O)=O InChI 1S/C6H13NO2/c1-3-4(2)5(7)6(8)9/h4-5H,3,7H2,1-2H3,(H,8,9)/t4-,5+/m1/s1 InChI key AGPKZVBTJJNPAG-UHNVWZDZSA-N
Safety InformationPersonal Protective Equipment Eyeshields,, Gloves,, type N95 (US), RIDADR NONH for all modes of transport WGK Germany WGK 1 Flash Point F Not applicable Flash Point C Not applicable Узнать цену -
L-Anserine nitrate salt
Empirical Formula (Hill Notation): C10H16N4O3 · HNO3 CAS Number: 10030-52-1 Molecular Weight: 303.27 EC Number: 233-079-7 MDL number: MFCD00037001 PubChem Substance ID: 24890509 NACRES: NA.26
Кат. номер A1131-100MG A1131-250MG A1131-5MG A1131-25MG A1131-500MG A1131-1G Biochem/physiol ActionsL-Anserine s a dipeptide found in most animal tissues. In model systems it is a potent antioxidant and scavener of hydroxyl radicals. It inhibits nonenzymatic protein glycation induced by aldose and ketose reducing sugars. It is much less potent than L-carnosine as an inhibitor of protein-protein crosslinking.LinkageAnserine is a naturally occurring methylated analog of carnosine.ПараметрыQuality Level 200, assay 98% form powder application(s) detection: suitable color white SMILES string O[N+]([O-])=O.Cn1cncc1C[C@H](NC(=O)CCN)C(O)=O InChI 1S/C10H16N4O3.HNO3/c1-14-6-12-5-7(14)4-8(10(16)17)13-9(15)2-3-11;2-1(3)4/h5-6,8H,2-4,11H2,1H3,(H,13,15)(H,16,17);(H,2,3,4)/t8-;/m0./s1 InChI key OLWOKAYJAHHSNY-QRPNPIFTSA-N
Safety Informationpictograms GHS07 signalword Warning hcodes H315 - H319 - H335 pcodes P302 + P352 - P305 + P351 + P338 Target Organs Respiratory system RIDADR NONH for all modes of transport WGK Germany WGK 3 Flash Point F Not applicable Flash Point C Not applicable Узнать цену -
L-Argininamide dihydrochloride
Empirical Formula (Hill Notation): C6H15N5O · 2HCl CAS Number: 14975-30-5 Molecular Weight: 246.14 MDL number: MFCD00058286 PubChem Substance ID: 24890827 NACRES: NA.26
Кат. номер A3913-1G A3913-5G A3913-25G Biochem/physiol ActionsL-Argininamide (L-Arm) is used as a model compound in studies of the physicochemical characteristic of ligand binding DNA aptamers and their potential development as fluorescent aptasensors.Параметрыassay 98% Quality Level 200, form powder application(s) ligand binding assay: suitable color white to off-white storage temp. 20°C SMILES string Cl.N[C@@H](CCCNC(N)=N)C(N)=O InChI 1S/C6H15N5O.ClH/c7-4(5(8)12)2-1-3-11-6(9)10;/h4H,1-3,7H2,(H2,8,12)(H4,9,10,11);1H/t4-;/m0./s1 InChI key BPQLYFCEVVKLLX-WCCKRBBISA-N
Safety Informationpictograms GHS07,GHS08 signalword Danger hcodes H302 - H370 pcodes P260 - P264 - P270 - P301 + P312 - P308 + P311 - P405 Target Organs Eyes Personal Protective Equipment Eyeshields,, Faceshields,, Gloves,, type P2 (EN 143) respirator cartridges, RIDADR NONH for all modes of transport WGK Germany WGK 2 Flash Point F Not applicable Flash Point C Not applicable Узнать цену -
L-Arginine
Empirical Formula (Hill Notation): C6H14N4O2 Linear Formula: H2NC(=NH)NH(CH2)3CH(NH2)CO2H CAS Number: 74-79-3 Molecular Weight: 174.20 Beilstein/REAXYS Number: 1725413 EC Number: 200-811-1 MDL number: MFCD00002635 eCl@ss: 32160406 PubChem Substance ID: 24278014 NACRES: NA.26
Кат. номер A5006-100G A5006-VAR A5006-500G A5006-1KG A5006-25G ApplicationL-arginine has been used to study non-enzymatic gluconeogenesis. It has also been used to study the effects of L-arginine supplementation on kidney and liver injury in rats with myocardial infarction.Packaging1 kg in poly bottle
100, 500 g in poly bottleBiochem/physiol ActionsL-Arginine is a dibasic, semi-essential amino acid. It acts as a precursor for creatinine and is a natural constituent of most of the dietary proteins.
Substrate of nitric oxide synthase, which is converted to citrulline and nitric oxide (NO). Induces insulin release by a nitric oxide-dependent mechanism.ПараметрыQuality Level 200 grade reagent grade assay 98% form powder application(s) cell analysis: suitable, peptide synthesis: suitable color white mp 222 °C (dec.) (lit.) solubility H2O: 50 mg/mL SMILES string N[C@@H](CCCNC(N)=N)C(O)=O InChI 1S/C6H14N4O2/c7-4(5(11)12)2-1-3-10-6(8)9/h4H,1-3,7H2,(H,11,12)(H4,8,9,10)/t4-/m0/s1 InChI key ODKSFYDXXFIFQN-BYPYZUCNSA-N Gene Information human ... NOS1(4842), NOS2(4843)
rat ... Ppm1a(24666)
Safety InformationPersonal Protective Equipment Eyeshields, Gloves, type N95 (US) RIDADR NONH for all modes of transport WGK Germany WGK 1 Flash Point(F) Not applicable Flash Point(C) Not applicable Узнать цену -
L-Arginine ethyl ester dihydrochloride
Empirical Formula (Hill Notation): C8H18N4O2 · 2HCl CAS Number: 36589-29-4 Molecular Weight: 275.18 MDL number: MFCD00038949 PubChem Substance ID: 24890700
Кат. номер A2883-5G A2883-25G A2883-100G Параметрыassay 98% Quality Level 200, form powder color white storage temp. 20°C SMILES string Cl.CCOC(=O)C(N)CCCNC(N)=N InChI 1S/C8H18N4O2.ClH/c1-2-14-7(13)6(9)4-3-5-12-8(10)11;/h6H,2-5,9H2,1H3,(H4,10,11,12);1H InChI key DUCUWLZKZPQJDY-UHFFFAOYSA-N
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L-Arginine methyl ester dihydrochloride
Empirical Formula (Hill Notation): C7H16N4O2 · 2HCl Linear Formula: HN=C(NH2)NH(CH2)3CH(NH2)COOCH3 · 2HCl CAS Number: 26340-89-6 Molecular Weight: 261.15 Beilstein/REAXYS Number: 4159929 EC Number: 247-622-0 MDL number: MFCD00038948 PubChem Substance ID: 57646878 NACRES: NA.22
Кат. номер 11030-5G 11030-25G ПараметрыQuality Level 100, assay 98.0% (AT) form powder optical activity []20/D +21±1°, c = 2.5% in methanol reaction suitability reaction type: solution phase peptide synthesis application(s) peptide synthesis: suitable color white mp ~190 °C (dec.) SMILES string Cl.Cl.COC(=O)[C@@H](N)CCCNC(N)=N InChI 1S/C7H16N4O2.2ClH/c1-13-6(12)5(8)3-2-4-11-7(9)10;;/h5H,2-4,8H2,1H3,(H4,9,10,11);2*1H/t5-;;/m0../s1 InChI key XQYZOBNLCUAXLF-XRIGFGBMSA-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 -
L-Arginine monohydrochloride
Empirical Formula (Hill Notation): C6H14N4O2 · HCl CAS Number: 1119-34-2 Molecular Weight: 210.66 Beilstein/REAXYS Number: 3631658 EC Number: 214-275-1 MDL number: MFCD00064550 PubChem Substance ID: 24890944 NACRES: NA.26
Кат. номер A5131-1G A5131-VAR A5131-10G A5131-1KG A5131-25KG A5131-100G A5131-25G A5131-1G-KC A5131-500G A5131-100KG ApplicationL-Arginine monohydrochloride has been used to study the effects of amino acids in promoting food consumption in Drosophila melanogaster. It has also been used to develop a non-invasive chronic pancreatitis model of rat.Packaging25 kg in poly drum
1 kg in poly bottle
10, 25, 100, 500 g in poly bottleBiochem/physiol ActionsL-Arginine is a semi-essential amino acid. This dibasic amino acid acts as a precursor for creatinine and is a natural constituent of most of the dietary proteins.
Substrate of nitric oxide synthase, which is converted to citrulline and nitric oxide (NO). Induces insulin release by a nitric oxide-dependent mechanism.Параметрыgrade reagent grade Quality Level 200, assay 98% (HPLC) form powder application(s) cell analysis: suitable color white mp >235 °C solubility H2O: 50 mg/mL SMILES string Cl[H].N[C@@H](CCCNC(N)=N)C(O)=O InChI 1S/C6H14N4O2.ClH/c7-4(5(11)12)2-1-3-10-6(8)9;/h4H,1-3,7H2,(H,11,12)(H4,8,9,10);1H/t4-;/m0./s1 InChI key KWTQSFXGGICVPE-WCCKRBBISA-N
Safety InformationPersonal Protective Equipment dust mask type N95 (US),, Eyeshields,, Gloves, RIDADR NONH for all modes of transport WGK Germany WGK 1 Flash Point F Not applicable Flash Point C Not applicable Узнать цену -
L-Argininosuccinic acid lithium salt
Empirical Formula (Hill Notation): C10H18N4O6 · xLi+ Molecular Weight: 290.27 (free acid basis) Beilstein/REAXYS Number: 6933810 PubChem Substance ID: 329764608 NACRES: NA.26
Кат. номер 73097-10MG 73097-50MG Biochem/physiol ActionsArginosuccinic acid is a basic amino acid, which is synthesized by some cells from citrulline, aspartic acid and used as a precursor for arginine in the urea cycle or Citrulline-NO cycle. The reaction is catalyzed by the enzyme argininosuccinate synthetase. Argininosuccinic acid is a precursor to fumarate in the citric acid cycle via argininosuccinate lyase. Defects in the arginosuccinate lyase enzyme can lead to arginosuccinate lyase deficiency. Argininosuccinate (ASA) lyase deficiency results in defective cleavage of ASA. This leads to an accumulation of ASA in cells and an excessive excretion of ASA in urine (arginosuccinic aciduria). In virtually all respects, this disorder shares the characteristics of other urea cycle defects. The most important characteristic of ASA lyase deficiency is its propensity to cause hyperammonemia in affected individuals. ASA in affected individuals is excreted by the kidney at a rate practically equivalent to the glomerular filtration rate (GFR). Whether ASA itself causes a degree of toxicity due to hepatocellular accumulation is unknown; such an effect could help explain hyperammonemia development in affected individuals. Regardless, the name of the disease is derived from the rapid clearance of ASA in urine, although elevated levels of ASA can be found in plasma. ASA lyase deficiency is associated with high mortality and morbidity rates.ПараметрыQuality Level 100, assay 70% (qNMR), 95% (TLC) form powder or crystals optical activity []/D 15±2°, c = 1 in H2O impurities 20% water color white to off-white storage temp. 2-8°C SMILES string OC(C[C@@H](C(O)=O)NC(NCCC[C@H](N)C(O)=O)=N)=O.[Li+] InChI 1S/C10H18N4O6.Li/c11-5(8(17)18)2-1-3-13-10(12)14-6(9(19)20)4-7(15)16;/h5-6H,1-4,11H2,(H,15,16)(H,17,18)(H,19,20)(H3,12,13,14);/q;+1/t5-,6-;/m0./s1 InChI key MGJRREWOOITZBB-GEMLJDPKSA-N
Safety InformationRIDADR NONH for all modes of transport WGK Germany WGK 3 Узнать цену -
L-Asparagine
Empirical Formula (Hill Notation): C4H8N2O3 Linear Formula: H2NCOCH2CH(NH2)CO2H CAS Number: 70-47-3 Molecular Weight: 132.12 Beilstein/REAXYS Number: 1723527 EC Number: 200-735-9 MDL number: MFCD00064401 eCl@ss: 32160406 PubChem Substance ID: 24890464 NACRES: NA.26
Кат. номер A0884-1G-KC A0884-1KG A0884-100G A0884-10MG A0884-25G A0884-1G A0884-500G ApplicationL-asparagine has been used:- to identify and quantify free amino acids released upon oxidation of proteins and peptides by hydroxyl radicals
- to study the effects of amino acids in promoting food consumption in Drosophila melanogaster
- to study non-enzymatic gluconeogenesis
Packaging25, 100, 500 g in poly bottle
10 mg in glass bottle
1 kg in poly bottleBiochem/physiol ActionsL-asparagine is an uncharged derivative of aspartate. It possesses a polar side chain and is a non-essential amino acid.ПараметрыQuality Level 300, assay 98% (HPLC) form powder application(s) detection: suitable color white mp 235 °C (dec.) (lit.) SMILES string N[C@@H](CC(N)=O)C(O)=O InChI 1S/C4H8N2O3/c5-2(4(8)9)1-3(6)7/h2H,1,5H2,(H2,6,7)(H,8,9)/t2-/m0/s1 InChI key DCXYFEDJOCDNAF-REOHCLBHSA-N
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L-Asparagine monohydrate
Empirical Formula (Hill Notation): C4H8N2O3 · H2O Linear Formula: NH2COCH2CH(NH2)COOH · H2O CAS Number: 5794-13-8 Molecular Weight: 150.13 Beilstein/REAXYS Number: 1723527 EC Number: 200-735-9 MDL number: MFCD00151038 PubChem Substance ID: 24891338
Кат. номер A8381-100G A8381-1KG A8381-10G A8381-1G A8381-25G General descriptionAsparagine biosynthesis is catalyzed by glutamine-dependent asparagine synthetase in mammalian tissues. Elevated levels of free asparagine is observed in plants facing stress in the form of drought or high salt. It is also present in senescing leaves and germinating seeds.ApplicationL-Asparagine monohydrate has been used:- as a component of Sautons and chelated Sautons media for mycobacterial growth
- to test its effect in the induction of Ca2+ flux in rice roots using aequorin luminescence imaging
- as a component of fermentation medium for the Blakeslea trispora spores
Packaging100 g in poly bottle
1 kg in poly bottleBiochem/physiol ActionsAsparagine has high nitrogen to carbon ratio and is a key regulator for nitrogen storage and transport. Its thermal degradation in the presence of sugars leads to the acrylamide formation in foods. Asparagine serves as an amino acid exchange factor and is essential for amino acid homeostasis. It favors cancer cell proliferation.
L-Asparagine, a proteinogenic amino acid, is used in biomanufacturing cell culture systems for the production of therapeutic recombinant proteins and monoclonal antibodies and in cell culture based research.ПараметрыQuality Level 200, biological source synthetic assay 99% (TLC) form powder application(s) cell analysis: suitable, peptide synthesis: suitable color white to off-white mp 233-235 °C (lit.) SMILES string [H]O[H].N[C@@H](CC(N)=O)C(O)=O InChI 1S/C4H8N2O3.H2O/c5-2(4(8)9)1-3(6)7;/h2H,1,5H2,(H2,6,7)(H,8,9);1H2/t2-;/m0./s1 InChI key RBMGJIZCEWRQES-DKWTVANSSA-N
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L-Aspartic acid
Empirical Formula (Hill Notation): C4H7NO4 Linear Formula: HO2CCH2CH(NH2)CO2H CAS Number: 56-84-8 Molecular Weight: 133.10 Beilstein/REAXYS Number: 1723530 EC Number: 200-291-6 MDL number: MFCD00002616 eCl@ss: 32160406 PubChem Substance ID: 24277948 NACRES: NA.26
Кат. номер A9256-10MG A9256-1G-KC A9256-5KG A9256-1G A9256-10MG-KC A9256-1KG A9256-500G A9256-100G A9256-5G A9256-25G ApplicationL-aspartic acid has been used as one of the components of synthetic drop out media for culturing budding yeast. It has also been used to study non-enzymatic gluconeogenesis.Packaging1 kg in poly bottle
100, 500 g in poly bottle
5 kg in poly drumBiochem/physiol ActionsPrincipal neurotransmitter for fast synaptic excitation.
Aspartic acid is a non-essential amino acid. It is involved in the Urea cycle, Krebs cycle and in DNA metabolism.Параметрыgrade reagent grade Quality Level 200, assay 98% (HPLC) form powder, crystals or chunks color white to off-white mp >300 °C (dec.) (lit.) solubility H2O: 5 mg/mL, 0.5 M HCl: 50 mg/mL (with heat), 1 M NaOH: 50 mg/mL SMILES string N[C@@H](CC(O)=O)C(O)=O InChI 1S/C4H7NO4/c5-2(4(8)9)1-3(6)7/h2H,1,5H2,(H,6,7)(H,8,9)/t2-/m0/s1 InChI key CKLJMWTZIZZHCS-REOHCLBHSA-N Gene Information human ... CA1(759), CA2(760)
rat ... Grin2a(24409)
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L-Aspartic acid -(7-amido-4-methylcoumarin)
Empirical Formula (Hill Notation): C14H14N2O5 CAS Number: 133628-73-6 Molecular Weight: 290.27 MDL number: MFCD00236804 PubChem Substance ID: 24890500 NACRES: NA.26
Кат. номер A1057-50MG A1057-10MG Biochem/physiol ActionsL-Aspartic acid-β-7-amido-4-methylcoumarin is sensitive and specific fluorogenic substrate used to assay for lysosomal glycoasparaginase (aspartylglucosaminidase) activity and the diagnosis of aspartylglucosaminuria.
L-Aspartic acid β-(7-amido-4-methylcoumarin) is used as a fluorogenic substrate for studying the specificity and kinetics of lysosomal glycoasparaginase(s) (aspartylglucosaminidase) and L-asparaginase(s).ПараметрыQuality Level 200, assay 98% form powder application(s) ligand binding assay: suitable color white to off-white storage temp. 20°C SMILES string CC1=CC(=O)Oc2cc(NC(=O)C[C@H](N)C(O)=O)ccc12 InChI 1S/C14H14N2O5/c1-7-4-13(18)21-11-5-8(2-3-9(7)11)16-12(17)6-10(15)14(19)20/h2-5,10H,6,15H2,1H3,(H,16,17)(H,19,20)/t10-/m0/s1 InChI key ARZPQBJTLVVDNP-JTQLQIEISA-N
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L-Aspartic acid -benzyl ester
Empirical Formula (Hill Notation): C11H13NO4 Linear Formula: C6H5CH2OCOCH2CH(NH2)COOH CAS Number: 2177-63-1 Molecular Weight: 223.23 Beilstein/REAXYS Number: 1983183 EC Number: 218-541-8 MDL number: MFCD00037208 PubChem Substance ID: 24891628 NACRES: NA.26
Кат. номер B2129-25G B2129-1G B2129-5G ApplicationL-Aspartic acid β-benzyl ester is used in the synthesis of peptides with a 1,4-diazepine-2,5-dione ring structure and in development of block copolymers.Параметрыassay 98% Quality Level 200, form powder application(s) peptide synthesis: suitable color white mp 225 °C storage temp. 20°C SMILES string N[C@@H](CC(=O)OCc1ccccc1)C(O)=O InChI 1S/C11H13NO4/c12-9(11(14)15)6-10(13)16-7-8-4-2-1-3-5-8/h1-5,9H,6-7,12H2,(H,14,15)/t9-/m0/s1 InChI key VGALFAWDSNRXJK-VIFPVBQESA-N
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L-Aspartic acid -hydroxamate
Empirical Formula (Hill Notation): C4H8N2O4 CAS Number: 1955-68-6 Molecular Weight: 148.12 MDL number: MFCD00050389 eCl@ss: 32160406 PubChem Substance ID: 24891095 NACRES: NA.26
Кат. номер A6508-1G-PW A6508-100MG A6508-1G A6508-100MG-PW ПараметрыQuality Level 200, assay >98% form powder application(s) detection: suitable color white to yellow storage temp. 20°C SMILES string N[C@@H](CC(=O)NO)C(O)=O InChI 1S/C4H8N2O4/c5-2(4(8)9)1-3(7)6-10/h2,10H,1,5H2,(H,6,7)(H,8,9)/t2-/m0/s1 InChI key ZBYVTTSIVDYQSO-REOHCLBHSA-N
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L-Aspartic acid 4-tert-butyl ester 11214-5G
Empirical Formula (Hill Notation): C8H15NO4 CAS Number: 3057-74-7 Molecular Weight: 189.21 Beilstein/REAXYS Number: 4671089 EC Number: 221-292-8 MDL number: MFCD00038577 PubChem Substance ID: 57646897 NACRES: NA.22 ПараметрыQuality Level 100, assay 98.0% (TLC) optical activity []20/D 9±2°, c = 2% in methanol: water (4:1) reaction suitability reaction type: solution phase peptide synthesis application(s) peptide synthesis: suitable color white SMILES string CC(C)(C)OC(=O)C[C@H](N)C(O)=O InChI 1S/C8H15NO4/c1-8(2,3)13-6(10)4-5(9)7(11)12/h5H,4,9H2,1-3H3,(H,11,12)/t5-/m0/s1 InChI key MXWMFBYWXMXRPD-YFKPBYRVSA-N
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L-Aspartic acid hemimagnesium salt dihydrate
Empirical Formula (Hill Notation): C8H12MgN2O8 · 2H2O Linear Formula: [HOOCCH(NH2)CH2COO]2Mg · 2H2O CAS Number: 215533-00-9 Molecular Weight: 324.53 Beilstein/REAXYS Number: 5178578 MDL number: MFCD00044935 eCl@ss: 32160406 PubChem Substance ID: 329749340 NACRES: NA.77
Кат. номер 11260-VAR 11260-100G 11260-500G ПараметрыQuality Level 200, assay 97.0% (KT) form powder or crystals optical activity []20/D +20±1°, c = 8% in 6 M HCl application(s) peptide synthesis: suitable color white to faint beige SMILES string [Mg++].N[C@@H](CC(O)=O)C([O-])=O.N[C@@H](CC(O)=O)C([O-])=O InChI 1S/2C4H7NO4.Mg/c2*5-2(4(8)9)1-3(6)7;/h2*2H,1,5H2,(H,6,7)(H,8,9);/q;;+2/p-2/t2*2-;/m00./s1 InChI key RXMQCXCANMAVIO-CEOVSRFSSA-L
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L-Aspartic acid potassium salt
Empirical Formula (Hill Notation): C4H6KNO4 Linear Formula: HO2CCH2CH(NH2)CO2K CAS Number: 1115-63-5 Molecular Weight: 171.19 EC Number: 214-226-4 MDL number: MFCD00063085 eCl@ss: 32160406 PubChem Substance ID: 24891105 NACRES: NA.77
Кат. номер A6558-100G A6558-25G A6558-1KG A6558-5G A6558-5KG General descriptionL-aspartic acid is a non-essential amino acid.ApplicationL-Aspartic acid potassium salt has been used:- to prepare perforated patch-clamp intracellular solution
- in serum glutamate–oxaloacetate transaminase (SGOT) assay
- as a component in an internal solution (IS) for mitoflash assay to detect mitochondrial flashes in permeabilized cells
Packaging25, 100 g in poly bottle
1 kg in poly bottleBiochem/physiol ActionsL-Aspartic acid is an endogenous N-methyl-D-aspartate (NMDA) receptor agonist.
Potassium aspartate is capable of preventing ventricular arrhythmia in ischemic rabbit heart by decreasing transmural repolarization dispersion (TDR).
Principal neurotransmitter for fast synaptic excitation.ПараметрыQuality Level 200, assay 98% (HPLC) form powder application(s) ligand binding assay: suitable color white SMILES string N[C@H](C([O-])=O)CC(O)=O.[K+] InChI 1S/C4H7NO4.K/c5-2(4(8)9)1-3(6)7;/h2H,1,5H2,(H,6,7)(H,8,9);/q;+1/p-1/t2-;/m0./s1 InChI key TXXVQZSTAVIHFD-DKWTVANSSA-M
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L-Aspartic acid sodium salt monohydrate
Empirical Formula (Hill Notation): C4H6NNaO4 · H2O Linear Formula: HO2CCH2CH(NH2)CO2Na · H2O CAS Number: 323194-76-9 Molecular Weight: 173.10 Beilstein/REAXYS Number: 6101944 EC Number: 223-264-0 MDL number: MFCD00152960 eCl@ss: 32160406 PubChem Substance ID: 24891129 NACRES: NA.32
Кат. номер A6683-25G A6683-1KG A6683-100G General descriptionAspartic acid is a non-essential amino acid. L-Aspartic acid is a dicarboxylic amino acid, which is involved in the synthesis of nerve cells proteins. It also stimulates the depolarization of nerve cell membranes. L-Aspartic acid acts as an amine donor for transamination reaction.ApplicationL-Aspartic acid sodium salt monohydrate has been as a component of reservoir solution for crystallization.Biochem/physiol ActionsSelective outflow of L-aspartic acid across the blood-brain barrier controls the level of L and D aspartic acid in the brain. Increased levels of L-aspartic acid in the brain results in excitatory neurotoxicity. Recent studies highlight that racemization of L-aspartic acid is followed by the determination of D:L ratio to estimate the age of an individual.
Principal neurotransmitter for fast synaptic excitation.ПараметрыQuality Level 200, assay 98% (TLC) form powder color white SMILES string [Na+].[H]O[H].N[C@@H](CC(O)=O)C([O-])=O InChI 1S/C4H7NO4.Na.H2O/c5-2(4(8)9)1-3(6)7;;/h2H,1,5H2,(H,6,7)(H,8,9);;1H2/q;+1;/p-1/t2-;;/m0../s1 InChI key PPTHNBYUFXSJPS-JIZZDEOASA-M Gene Information human ... GRIN2A(2903)
rat ... GRIN2A(14811)
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L-C-Propargylglycine
Empirical Formula (Hill Notation): C5H7NO2 CAS Number: 23235-01-0 Molecular Weight: 113.11 Beilstein/REAXYS Number: 2347861 MDL number: MFCD00077855 eCl@ss: 32160406 PubChem Substance ID: 57652892 NACRES: NA.26
Кат. номер 81838-250MG 81838-50MG ApplicationReagent for the irreversible inactivation of γ-cystathionase; affinity labeling reagent for γ-cystathionase and other enzymes; peptides containing this amino acid can be tritiated to high specific radioactivityBiochem/physiol ActionsL-C-Propargylglycine, a specific inhibitor of H(2)S synthase of cystathionine-γ-lyase (CSE), may be used to study the role of H2S in regulation of biological processes.
L-propargylglycine (PAG), an inhibitor of cystathionine γ-lyase (CSE), is useful in studies of hydrogen sulphide synthesis and bioactivity.ПараметрыQuality Level 100, assay 99.0% (TLC) form powder application(s) peptide synthesis: suitable color white mp 235-239 °C storage temp. 2-8°C SMILES string N[C@@H](CC#C)C(O)=O InChI 1S/C5H7NO2/c1-2-3-4(6)5(7)8/h1,4H,3,6H2,(H,7,8)/t4-/m0/s1 InChI key DGYHPLMPMRKMPD-BYPYZUCNSA-N
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L-Canavanine
Empirical Formula (Hill Notation): C5H12N4O3 CAS Number: 543-38-4 Molecular Weight: 176.17 MDL number: MFCD00055781 PubChem Substance ID: 24892427 NACRES: NA.26
Кат. номер C1625-1G C1625-100MG C1625-250MG C1625-25MG Packaging100, 250 mg in poly bottle
1 g in poly bottleBiochem/physiol ActionsCanavanine is a naturally occurring L-amino acid that interferes with L-arginine-utilizing enzymes due to its structural similarity. It is a selective inhibitor of inducible nitric oxide synthase (iNOS). Overproduction of NO by iNOS plays a crucial role in the pathophysiology of septic shock and chronic inflammation.
A naturally occurring L-amino acid that interferes with L-arginine-utilizing enzymes due to its structural similarity. It is a selective inhibitor of inducible nitric oxide synthase (iNOS). Overproduction of NO by iNOS plays a crucial role in the pathophysiology of septic shock and chronic inflammation.Other NotesTandem Mass Spectrometry data independently generated by Scripps Center for Metabolomics is available to view or download in PDF. C1625.pdf , Tested metabolites are featured on Scripps Center for Metabolomics METLIN Metabolite Database. To learn more, visit sigma.com/metlin.,Параметрыbiological source Canavalia ensiformis Quality Level 200, assay 98% (TLC) form powder application(s) detection: suitable color white to yellow solubility H2O: <100 mg/mL storage temp. 2-8°C SMILES string N[C@@H](CCONC(N)=N)C(O)=O InChI 1S/C5H12N4O3/c6-3(4(10)11)1-2-12-9-5(7)8/h3H,1-2,6H2,(H,10,11)(H4,7,8,9)/t3-/m0/s1 InChI key FSBIGDSBMBYOPN-VKHMYHEASA-N
Safety Informationpictograms GHS07 signalword Warning hcodes H302 + H312 + H332 pcodes P261 - P264 - P280 - P301 + P312 - P302 + P352 + P312 - P304 + P340 + P312 Personal Protective Equipment dust mask type N95 (US),, Eyeshields,, Gloves, RIDADR NONH for all modes of transport WGK Germany WGK 3 Узнать цену -
L-Carnitine 11242008001
General descriptionEnzymatic UV-Test with a linearity in the range of 5.6 - 112 μM L-carnitine in the test solution.ApplicationDetermination of L-carnitine in seminal plasma, serum, or urine in life science research applications.Biochem/physiol ActionsL-carnitine is an abundant amino acid present in red meat. Its trimethylamine structure has similarity to that of choline. The major source of this amino acid is by dietary ingestion. In mammals, it is also endogenously produced from lysine. It participates in the transport of fatty acids into the mitochondrial compartment. It produces trimethylamine-N-oxide (TMAO) and promotes atherosclerosis.Packaging1 kit containing 6 componentsPrincipleL-Carnitine is acetylated to acetyl carnitine by acetyl coenzyme A (acetyl CoA) in the presence of the enzyme carnitine acetyl transferase (CAT). The resulting coenzyme A (CoA) is acetylated back to acetyl CoA in the presence of adenosine-5-triphosphate (ATP) and acetate, catalyzed by the enzyme acetyl CoA synthetase (ACS). This results in the formation of adenosine-5-monophosphate (AMP) and inorganic pyrophosphate (PPi). In the presence of ATP, supported by myokinase (MK), AMP forms twice the amount of adenosine-5-diphosphate (ADP). This is converted in the following reaction with phosphoenol pyruvate (PEP) in the presence of pyruvate kinase (PK). The pyruvate formed is reduced to L-lactate by reduced nicotinamide adenine dinucleotide (NADH) in the presence of lactate dehydrogenase (LDH). The amount of NADH consumed during the reaction is equivalent to half the amount of L-carnitine. NADH is measured spectroscopically at 340 nm.Preparation NoteStorage conditions (working solution): Note:- After reconstitution, the solution 1 is stable for 4 days at 2 to 8 °C.
- Bring solution 1 to 15 to 25 °C prior to use.
- After reconstitution, the suspension 2 is stable for 3 months at 2 to 8 °C.
Other NotesFor life science research only. Not for use in diagnostic procedures.Параметрыusage sufficient for ~3 x 10 determinations (test-combination), sufficient for ~3 x 10 tests Торговая марка Roche shipped in wet ice storage temp. 2-8°C
Safety Informationpictograms GHS05 signalword Danger hcodes H318 - H412 pcodes P273 - P280 - P305 + P351 + P338 + P310 - P501 RIDADR NONH for all modes of transport WGK Germany WGK 2 Flash Point F does not flash Flash Point C does not flash Узнать цену -
L-Carnitine hydrochloride
Empirical Formula (Hill Notation): C7H15NO3 · HCl Linear Formula: (CH3)3N+CH2CH(OH)CH2CO2H · Cl- CAS Number: 6645-46-1 Molecular Weight: 197.66 EC Number: 229-663-6 MDL number: MFCD00066100 PubChem Substance ID: 24892246 NACRES: NA.79
Кат. номер C0283-10MG C0283-1G C0283-5G C0283-25G C0283-100G ApplicationL-Carnitine hydrochloride has been used to study ergothioneine transporter SLC22A4 and carnitine transporter SLC22A5. It has also been used to allow the entry of palmitic acid into the mitochondria.Packaging10 mg in glass bottle
1, 5, 25, 100 g in poly bottleBiochem/physiol ActionsCarnitine is biosynthesized from lysine. It might be associated with the energy production from branched chain amino acids.
Carnitine is a quaternary amine that occurs naturally in most mammalian tissue. It is present in relatively high concentrations in skeletal muscle and heart where it is involved in regulating energy metabolism. It shifts glucose metabolism from glycolysis to glycogen storage and enhances the transport of long chain fatty acids into the mitochondria where they are oxidized for energy production.ПараметрыQuality Level 200, biological source synthetic assay 98% form powder application(s) cell analysis: suitable color white mp 142 °C SMILES string [Cl-].C[N+](C)(C)C[C@H](O)CC(O)=O InChI 1S/C7H15NO3.ClH/c1-8(2,3)5-6(9)4-7(10)11;/h6,9H,4-5H2,1-3H3;1H/t6-;/m1./s1 InChI key JXXCENBLGFBQJM-FYZOBXCZSA-N
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L-Carnitine inner salt
Empirical Formula (Hill Notation): C7H15NO3 Linear Formula: (CH3)3N+CH2CH(OH)CH2COO- CAS Number: 541-15-1 Molecular Weight: 161.20 Beilstein/REAXYS Number: 4292315 EC Number: 208-768-0 MDL number: MFCD00038747 PubChem Substance ID: 24892238 NACRES: NA.79
Кат. номер C0158-25G C0158-1G C0158-5G C0158-100G ApplicationL-Carnitine inner salt has been used as a component of an assay medium for Seahorse XF mitochondrial stress assay. It has also been orally administered to tumor-bearing mice, in order to study its effect on the regulation of peroxisome proliferator-activated receptor and thereby to analyse liver inflammatory response.Packaging1, 5, 25, 100 g in poly bottleBiochem/physiol ActionsCarnitine biosynthesized from lysine. Carnitine facilitates fatty acid transport into the mitochondrial compartment. In skeletal and cardiac muscle tissue it acts as a metabolic cofactor. Carnitine might be associated with the energy production from branched chain amino acids.
Carnitine is a quaternary amine that occurs naturally in most mammalian tissue. It is present in relatively high concentrations in skeletal muscle and heart where it is involved in regulating energy metabolism. It shifts glucose metabolism from glycolysis to glycogen storage and enhances the transport of long chain fatty acids into the mitochondria where they are oxidized for energy production.ПараметрыQuality Level 200, biological source synthetic assay 98% form powder application(s) cell analysis: suitable, detection: suitable color white mp 197-212 °C (lit.) SMILES string C[N+](C)(C)C[C@H](O)CC([O-])=O InChI 1S/C7H15NO3/c1-8(2,3)5-6(9)4-7(10)11/h6,9H,4-5H2,1-3H3/t6-/m1/s1 InChI key PHIQHXFUZVPYII-ZCFIWIBFSA-N
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L-Carnosine
Empirical Formula (Hill Notation): C9H14N4O3 CAS Number: 305-84-0 Molecular Weight: 226.23 Beilstein/REAXYS Number: 87671 EC Number: 206-169-9 MDL number: MFCD00005207 PubChem Substance ID: 24893178 NACRES: NA.26
Кат. номер C9625-25G C9625-100G C9625-5G C9625-10MG C9625-1G C9625-500MG Amino Acid SequenceAla-HisApplicationL-Carnosine has been used to study its effects as an antioxidant on meat quality of pigs. It has also been used to study its effects on brain injury in a rat intracerebral hemorrhage model.Packaging5, 25, 100 g in poly bottle
10 mg in poly bottleBiochem/physiol ActionsL-Carosine is a dipeptide found at millimolar concentration in brain, muscle and the lens of the eye. In model systems it is a potent antioxidant that scavenges oxygen free radicals and transition metal ions. It blocks protein-protein and protein-DNA cross-links induced by hypochlorite anions and toxic aldehydes such as acetaldehyde, formaldehyde, and malondialdehyde, the primary product of lipid peroxidation. It also inhibits nonenzymatic protein glycation induced by aldose and ketose reducing sugars and inhibits the formation of toxic advanced glycation end products (AGE). These activities make it of interest in studies of aging, atherosclerosis, Alzheimers disease, and the secondary effects of diabetes.
Dipeptide with potent antioxidant and antiglycation activity; blocks nonenzymatic glycosylation and protein cross-linking induced by reactive aldehydes.Other NotesTandem Mass Spectrometry data independently generated by Scripps Center for Metabolomics is available to view or download in PDF. C9625.pdf , Tested metabolites are featured on Scripps Center for Metabolomics METLIN Metabolite Database. To learn more, visit sigma.com/metlin.,Параметрыassay ~99% Quality Level 200, form crystalline application(s) cell analysis: suitable color white to off-white mp 253 °C (dec.) (lit.) storage temp. 20°C SMILES string NCCC(=O)N[C@@H](Cc1c[nH]cn1)C(O)=O InChI 1S/C9H14N4O3/c10-2-1-8(14)13-7(9(15)16)3-6-4-11-5-12-6/h4-5,7H,1-3,10H2,(H,11,12)(H,13,14)(H,15,16)/t7-/m0/s1 InChI key CQOVPNPJLQNMDC-ZETCQYMHSA-N Gene Information human ... CA1(759), CA2(760)
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L-Citrulline
Empirical Formula (Hill Notation): C6H13N3O3 CAS Number: 372-75-8 Molecular Weight: 175.19 Beilstein/REAXYS Number: 1725416 EC Number: 206-759-6 MDL number: MFCD00064397 PubChem Substance ID: 24892975 NACRES: NA.32
Кат. номер C7629-500G C7629-25G C7629-1G C7629-10MG C7629-1KG C7629-5G C7629-10MG-KC C7629-100G ApplicationL-Citrulline has been used in ultra-performance liquid chromatography to validate, metabolites involved in the coordination of metamorphic processes.Packaging10 mg in autosample vial
5, 25 g in poly bottleBiochem/physiol ActionsL-Citrulline, when orally administered is found to ameliorate the condition of sickle cell disease in humans. L-citrulline can be a replacement for L-arginine administration in case of defective NO synthetase. L-Citrulline supplementation is found to fulfill the purpose of NO-dependent signaling.
Intermediate in the production of nitric oxide from L-arginine by NO synthetase.Other NotesTandem Mass Spectrometry data independently generated by Scripps Center for Metabolomics is available to view or download in PDF. C7629.pdf , Tested metabolites are featured on Scripps Center for Metabolomics METLIN Metabolite Database. To learn more, visit sigma.com/metlin.,ПараметрыQuality Level 200, assay 98% (TLC) form powder application(s) detection: suitable color white to off-white SMILES string N[C@@H](CCCNC(N)=O)C(O)=O InChI 1S/C6H13N3O3/c7-4(5(10)11)2-1-3-9-6(8)12/h4H,1-3,7H2,(H,10,11)(H3,8,9,12)/t4-/m0/s1 InChI key RHGKLRLOHDJJDR-BYPYZUCNSA-N
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L-Cystathionine
Empirical Formula (Hill Notation): C7H14N2O4S CAS Number: 56-88-2 Molecular Weight: 222.26 Beilstein/REAXYS Number: 2505200 EC Number: 200-295-8 MDL number: MFCD00036685 PubChem Substance ID: 24892965 NACRES: NA.26
Кат. номер C7505-10MG C7505-50MG C7505-250MG ApplicationL-Cystathionine has been used in ultra-performance liquid chromatography for the validation of cystathionine and the correlation of its abundance with vertebrate metamorphosis. It has also been used as an inhibitor of sinusoidal GSH (glutathione) carrier to signify that thiol redox state imbalance is associated with the modulation of autophagy in carcinoma cells.Packaging10 mg in glass bottle
50, 250 mg in poly bottleBiochem/physiol ActionsL-Cystathionine is an intermediate in the biosynthesis of L-cysteine and methionine. It is used as a substrate to differentiate and analyze cystathionine γ-lyase(s). L-Cystathionine is an important non-protein amino acid and is associated with metabolic disorders. In recent studies, L-cystathionine is believed to be the precursor of cyclic imino acid cyclothionine. Cystathioninuria is characterized with imino acid cyclothionine excretion in the urine.Other NotesTandem Mass Spectrometry data independently generated by Scripps Center for Metabolomics is available to view or download in PDF. C7505.pdf , Tested metabolites are featured on Scripps Center for Metabolomics METLIN Metabolite Database. To learn more, visit sigma.com/metlin.,ПараметрыQuality Level 200, assay 98% (TLC) form powder application(s) UHPLC: suitable color white mp >300 °C storage temp. 20°C SMILES string N[C@@H](CCSC[C@H](N)C(O)=O)C(O)=O InChI 1S/C7H14N2O4S/c8-4(6(10)11)1-2-14-3-5(9)7(12)13/h4-5H,1-3,8-9H2,(H,10,11)(H,12,13)/t4-,5-/m0/s1 InChI key ILRYLPWNYFXEMH-WHFBIAKZSA-N
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L-Cysteic acid monohydrate
Empirical Formula (Hill Notation): C3H7NO5S · H2O Linear Formula: HO3SCH2CH(NH2)CO2H·H2O CAS Number: 23537-25-9 Molecular Weight: 187.17 Beilstein/REAXYS Number: 3714036 MDL number: MFCD00149544 PubChem Substance ID: 24858207 NACRES: NA.26
Кат. номер 30170-10G 30170-INTR 30170-50G ApplicationInternal standard for amino acid analysis.Biochem/physiol ActionsL-cysteic acid is an oxidation product of L-cysteine. L-Cysteic acid, an analogue of cysteine sulfinic acid, may be used in studies of excitatory amino acids in the brain, such as those that bind to cysteine sulfinic acid receptors. L-Cysteic acid is a useful agonist at several rat metabotropic glutamate receptors (mGluRs).
L-Cysteic acid is a sulfur containing aspartate analogue that may be used as a competitive inhibitor of the bacterial aspartate:alanine antiporter (AspT) exchange of aspartate and in other aspartate biological systems. L-Cysteic acid is used in monomeric surfactant development.ПараметрыQuality Level 200, assay 99.0% (T) form powder or crystals optical activity []20/D +7.5±0.5°, c = 5% in H2O application(s) LC/MS: suitable, peptide synthesis: suitable color white to faint yellow mp 267 °C (dec.) (lit.) solubility H2O: soluble SMILES string [H]O[H].N[C@@H](CS(O)(=O)=O)C(O)=O InChI 1S/C3H7NO5S.H2O/c4-2(3(5)6)1-10(7,8)9;/h2H,1,4H2,(H,5,6)(H,7,8,9);1H2/t2-;/m0./s1 InChI key PCPIXZZGBZWHJO-DKWTVANSSA-N
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L-Cysteine
Empirical Formula (Hill Notation): C3H7NO2S Linear Formula: HSCH2CH(NH2)CO2H CAS Number: 52-90-4 Molecular Weight: 121.16 Beilstein/REAXYS Number: 1721408 EC Number: 200-158-2 MDL number: MFCD00064306 eCl@ss: 32160406 PubChem Substance ID: 24892959 NACRES: NA.75
Кат. номер C7352-100G C7352-10MG C7352-1G-KC C7352-1KG C7352-25G C7352-1G C7352-25KG General descriptionL-Cysteine is one of the sulfur containing proteinogenic amino acid incorporated into proteins as directed by the genetic code. The thiol-side chain participates in a variety of oxidation/reduction reactions within the cell. The side chain participates in the formation of bonds that modulate the secondary and ternary structure of proteins. L-Cysteine is an essential precursor for inorganic sulfates, coenzyme A. Cysteine is an essential and limiting for the formation of glutathione, an important antioxidant, within the cell. Mammalian liver can synthesize L-cysteine and is a semi-essential amino acid. L-cysteine prevents oxidation of nerve cells, aids in maintaining the stability and rigidity of connective tissues. L-cysteine speeds up the healing process of the body and reduces inflammatory reactions. L-cysteine protects testis partially against acrylamide induced toxicity. L-cysteine can prevent DNA damage during cryopreservation and preserves semen quality.
L-Cysteine is a proteinogenic amino acid incorporated into proteins as directed by the genetic code. The thiol-side chain participates in a variety of oxidation/reduction reactions within the cell. The side chain participates in the formation of β bonds that modulate the secondary and ternary structure of proteins. Cysteine is essential and limiting for the formation of glutathione, an important antioxidant, within the cell.ApplicationL-Cysteine has been used:- as a media supplement in Trypticase-Yeast Extract-Iron-Serum (TYI-S-33) media for the culture of Giardia lamblia, to make enzyme solution in Dulbeccos modified Eagles medium (DMEM) to establish hippocampus culture
- to test its protective effect on acrylamide induced toxicity in testis
- in the preparation of tris acetic acid extender solution for cryopreservation of semen
- as an additive to make papain digestion solution
Packaging10 mg in glass bottle
25, 100 g in poly bottle
1 kg in poly bottleBiochem/physiol ActionsNMDA glutamatergic receptor agonist.Other NotesL-Cysteine is used to supplement cell culture media. This product is a non-animal source amino acid useful for serum-free media formulations intended for biomanufacturing applications.
Tandem Mass Spectrometry data independently generated by Scripps Center for Metabolomics is available to view or download in PDF. C7352.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 non-animal source product line BioReagent assay 98% form crystalline powder application(s) cell culture | mammalian: suitable impurities endotoxin, tested color white mp 240 °C (dec.) (lit.) solubility H2O: 25 mg/mL SMILES string N[C@@H](CS)C(O)=O InChI 1S/C3H7NO2S/c4-2(1-7)3(5)6/h2,7H,1,4H2,(H,5,6)/t2-/m0/s1 InChI key XUJNEKJLAYXESH-REOHCLBHSA-N
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L-Cysteine ethyl ester hydrochloride
Empirical Formula (Hill Notation): C5H11NO2S · HCl Linear Formula: HSCH2CH(NH2)COOC2H5 · HCl CAS Number: 868-59-7 Molecular Weight: 185.67 Beilstein/REAXYS Number: 3562600 EC Number: 212-779-6 MDL number: MFCD00012631 eCl@ss: 32160406 PubChem Substance ID: 24892386 NACRES: NA.22
Кат. номер C121908-100G C121908-25G ПараметрыQuality Level 200, assay 98% optical activity []20/D 7.9°, c = 1 in 1 M HCl optical purity ee: 99% (GLC) reaction suitability reaction type: solution phase peptide synthesis application(s) peptide synthesis: suitable color white mp 123-125 °C (lit.) SMILES string Cl[H].CCOC(=O)[C@@H](N)CS InChI 1S/C5H11NO2S.ClH/c1-2-8-5(7)4(6)3-9;/h4,9H,2-3,6H2,1H3;1H/t4-;/m0./s1 InChI key JFKJWWJOCJHMGV-WCCKRBBISA-N
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L-Cysteine hydrochloride
Empirical Formula (Hill Notation): C3H7NO2S · HCl Linear Formula: HSCH2CH(NH2)COOH · HCl CAS Number: 52-89-1 Molecular Weight: 157.62 Beilstein/REAXYS Number: 3560277 EC Number: 200-157-7 MDL number: MFCD00064553 PubChem Substance ID: 24892395 NACRES: NA.32
Кат. номер C1276-1G C1276-1G-KC C1276-250G C1276-10G C1276-50G C1276-100G ApplicationL-Cysteine hydrochloride has been used as a supplement in media to study the metabolic and sleep phenotypes of Drosophila melanogaster. It has also been used as one of the reagents for cell dissociation and single cell collection.Biochem/physiol ActionsNMDA glutamatergic receptor agonist that is also an agonist at AMPA glutamatergic receptors at high concentrations.
Cysteine (Cys) is a functional sulfur-containing aminoacid that regulates metabolism for growth, reproduction and immunity. It provides the disulfide linkage in proteins and is involved in the transport of sulfur. Cysteine is involved in the formation of hydrogen sulfide that functions as a signaling molecule. Cys residues are present at the catalytic sites of various enzymes.ПараметрыQuality Level 100, grade anhydrous assay 98% (TLC) form powder application(s) UHPLC: suitable color white mp 174.1-174.7 °C solubility H2O: 50 mg/mL, clear, colorless SMILES string Cl[H].N[C@@H](CS)C(O)=O InChI 1S/C3H7NO2S.ClH/c4-2(1-7)3(5)6;/h2,7H,1,4H2,(H,5,6);1H/t2-;/m0./s1 InChI key IFQSXNOEEPCSLW-DKWTVANSSA-N Gene Information human ... AMPA 1(2890), GRIA2(2891), GRIA3(2892), GRIA4(2893), GRIN1(2902), GRIN2A(2903), GRIN2B(2904), GRIN2C(2905), GRIN2D(2906), GRIN3A(116443), GRIN3B(116444), GRINA(2907)
mouse ... AMPA 1(14799), GRIA2(14800), GRIA3(53623), GRIA4(14802), GRIN1(14810), GRIN2A(14811), GRIN2B(14812), GRIN2C(14813), GRIN2D(14814), GRIN3A(242443), GRIN3B(170483), GRINA(66168)
rat ... AMPA 1(50592), GRIA2(29627), GRIA3(29628), GRIA4(29629), GRIN1(24408), GRIN2A(24409), GRIN2B(24410), GRIN2C(24411), GRIN2D(24412), GRIN3A(191573), GRIN3B(170796), GRINA(266668)
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L-Cysteine hydrochloride hydrate
Empirical Formula (Hill Notation): C3H7NO2S · HCl · xH2O Linear Formula: HSCH2CH(NH2)CO2H·HCl·xH2O CAS Number: 345909-32-2 Molecular Weight: 157.62 (anhydrous basis) EC Number: 200-157-7 MDL number: MFCD00065606 eCl@ss: 32160406 PubChem Substance ID: 24892385 NACRES: NA.22
Кат. номер C121800-5G C121800-100G ПараметрыQuality Level 100, assay 99% optical activity []23/D +5.2°, c = 2 in 5 M HCl reaction suitability reaction type: solution phase peptide synthesis application(s) affinity chromatography: suitable, peptide synthesis: suitable color white storage temp. 2-8°C SMILES string Cl[H].[H]O[H].N[C@@H](CS)C(O)=O InChI 1S/C3H7NO2S.ClH.H2O/c4-2(1-7)3(5)6;;/h2,7H,1,4H2,(H,5,6);1H;1H2/t2-;;/m0../s1 InChI key QIJRTFXNRTXDIP-JIZZDEOASA-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 -
L-Cysteine hydrochloride monohydrate
Empirical Formula (Hill Notation): C3H7NO2S · HCl · H2O Linear Formula: HSCH2CH(NH2)COOH · HCl · H2O CAS Number: 7048-04-6 Molecular Weight: 175.63 Beilstein/REAXYS Number: 5158059 EC Number: 200-157-7 MDL number: MFCD00065606 eCl@ss: 32160406 PubChem Substance ID: 24892902 NACRES: NA.26
Кат. номер C6852-VAR C6852-100G C6852-25G C6852-1KG C6852-BR C6852-25KG ApplicationL-Cysteine hydrochloride monohydrate has been used as a component of yeast dropout media for culturing yeasts. It has also been used as a component of differential reinforced clostridial broth (DRCM) for the isolation of clostridia.Packaging25, 100 g in poly bottle
1 kg in poly bottleBiochem/physiol ActionsCysteine (Cys) is a sulfur-containing amino acid that modulates metabolism for growth, reproduction and immunity. It provides the disulfide linkage in proteins and in involved in the transport of sulfur. Cysteine is involved in the formation of hydrogen sulfide that functions as a signaling molecule. Cys residues are present at the catalytic sites of various enzymes.
NMDA glutamatergic receptor antagonist.Параметрыbiological source non-animal source Quality Level 200, Agency/Method meets EP testing specifications, meets USP testing specifications assay 98.5-101.0% dry basis form powder or crystals application(s) cell culture | mammalian: suitable impurities endotoxin, tested color white Featured Industry Pharmaceutical (small molecule) SMILES string O.Cl.N[C@@H](CS)C(O)=O InChI 1S/C3H7NO2S.ClH.H2O/c4-2(1-7)3(5)6;;/h2,7H,1,4H2,(H,5,6);1H;1H2/t2-;;/m0../s1 InChI key QIJRTFXNRTXDIP-JIZZDEOASA-N
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L-Cysteine S-sulfate
Empirical Formula (Hill Notation): C3H7NO5S2 CAS Number: 1637-71-4 Molecular Weight: 201.22 Beilstein/REAXYS Number: 1726832 MDL number: MFCD00133440 PubChem Substance ID: 24892471
Кат. номер C2196-25MG-PW C2196-5MG C2196-25MG C2196-5MG-PW Packaging5 mg in glass bottle
25 mg in poly bottleBiochem/physiol ActionsL-Cysteine S-sulfate (LCSS) is used as an NMDA glutamatergic receptor agonist. It serves as a substrate for cystine lyase(s).
Cysteine is one of the functional amino acids that are associated with growth, reproduction, maintenance and immunity. Cysteine is a source of disulfide linkage in protein and is associated with sulfur transport. At physiological pH, cysteine undergoes rapid oxidation to form cystine. Reduced availability of cysteine or cystine, influences leukocyte metabolism. L-Cysteine serves as a precursor for the rate limiting step in glutathione synthesis that occurs in neurons. It donates inorganic sulfate for detoxification reactions. Therefore, L-cysteine might be associated with neuroprotection. It is found to obstruct the entry of heavy metal ions across the blood-brain barrier into the brain. Increased levels of L-cysteine might lead to neurotoxicity.Other NotesTandem Mass Spectrometry data independently generated by Scripps Center for Metabolomics is available to view or download in PDF. C2196.pdf , Tested metabolites are featured on Scripps Center for Metabolomics METLIN Metabolite Database. To learn more, visit sigma.com/metlin.,ПараметрыQuality Level 200, assay 98% (TLC) form powder application(s) ligand binding assay: suitable color white storage temp. 20°C SMILES string N[C@@H](CSS(O)(=O)=O)C(O)=O InChI 1S/C3H7NO5S2/c4-2(3(5)6)1-10-11(7,8)9/h2H,1,4H2,(H,5,6)(H,7,8,9)/t2-/m0/s1 InChI key NOKPBJYHPHHWAN-REOHCLBHSA-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 -
L-Cystine
Empirical Formula (Hill Notation): C6H12N2O4S2 Linear Formula: [-SCH2CH(NH2)CO2H]2 CAS Number: 56-89-3 Molecular Weight: 240.30 Beilstein/REAXYS Number: 1728094 EC Number: 200-296-3 MDL number: MFCD00064228 eCl@ss: 32160406 PubChem Substance ID: 24893101 NACRES: NA.26
Кат. номер C8755-1G C8755-1G-KC C8755-500G C8755-100G C8755-1KG C8755-25G ApplicationL-Cystine has been used in in vitro cystine solubility assay to identify potential drugs that influence cystine solubility. It is also used as a supplement of phosphate-buffered saline to slice and wash periprosthetic tissues.Packaging1 kg in poly bottle
100, 500 g in poly bottleBiochem/physiol ActionsCysteine is the source of disulfide linkages in proteins and has a role in sulfur transport. It undergoes rapid oxidation to form cystine at physiological pH. L-cystine is crucial for oxygen production and low density lipoprotein modification by arterial smooth muscle cells. It also has a role in the synthesis of glutathione.Параметрыbiological source human hair Quality Level 200, assay 98% (TLC) form crystalline application(s) cell analysis: suitable, peptide synthesis: suitable color white to off-white mp >240 °C (dec.) (lit.) solubility 1 M HCl: 50 mg/mL, clear, colorless to faintly yellow storage temp. room temp SMILES string N[C@@H](CSSC[C@H](N)C(O)=O)C(O)=O InChI 1S/C6H12N2O4S2/c7-3(5(9)10)1-13-14-2-4(8)6(11)12/h3-4H,1-2,7-8H2,(H,9,10)(H,11,12)/t3-,4-/m0/s1 InChI key LEVWYRKDKASIDU-IMJSIDKUSA-N
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L-Cystine dihydrochloride
Empirical Formula (Hill Notation): C6H12N2O4S2 · 2HCl CAS Number: 30925-07-6 Molecular Weight: 313.22 EC Number: 250-391-9 MDL number: MFCD00070399 PubChem Substance ID: 24892885 NACRES: NA.26
Кат. номер C6727-100G C6727-1KG C6727-25G C6727-25KG C6727-BR ApplicationNon-animal sourced L-cystine is used as a cell culture media component for the commercial biomanufacture of therapeutic recombinant proteins and monoclonal antibodies.Packaging25, 100 g in poly bottle
1 kg in poly bottleBiochem/physiol ActionsCystine is the dimeric form of cysteine. Cysteine is the source of disulfide linkages in proteins and has a role in sulfur transport. It undergoes rapid oxidation to form cystine at physiological pH. L-Cystine is crucial for oxygen production and low density lipoprotein modification by arterial smooth muscle cells. It also has a role in the synthesis of glutathione.CautionhygroscopicПараметрыbiological source non-animal source Quality Level 200, product line BioReagent assay 98.0% dry basis form crystalline powder application(s) cell culture | mammalian: suitable impurities endotoxin, tested color white to off-white mp 211.36 °C solubility 2 M HCl: 50 mg/mL SMILES string Cl.Cl.N[C@@H](CSSC[C@H](N)C(O)=O)C(O)=O InChI 1S/C6H12N2O4S2.2ClH/c7-3(5(9)10)1-13-14-2-4(8)6(11)12;;/h3-4H,1-2,7-8H2,(H,9,10)(H,11,12);2*1H/t3-,4-;;/m0../s1 InChI key HHGZUQPEIHGQST-RGVONZFCSA-N
Safety Informationpictograms GHS05 signalword Danger hcodes H314 pcodes P260 - P280 - P303 + P361 + P353 - P305 + P351 + P338 + P310 Personal Protective Equipment Eyeshields,, Gloves,, type N95 (US), RIDADR NONH for all modes of transport WGK Germany WGK 1 Flash Point F Not applicable Flash Point C Not applicable Узнать цену -
L-Ethionine
Empirical Formula (Hill Notation): C6H13NO2S Linear Formula: C2H5SCH2CH2CH(NH2)CO2H CAS Number: 13073-35-3 Molecular Weight: 163.24 EC Number: 235-966-4 MDL number: MFCD00002626 PubChem Substance ID: 24894397
Кат. номер E1260-250MG E1260-1G E1260-5G Packaging250 mg in poly bottle
1 g in poly bottleBiochem/physiol ActionsAn analog of methionine that interferes with the normal methylation of DNA and other methylation pathways, and induces pancreatic toxicity and liver cancer. However, in animal studies, it has also been shown to act synergistically with methionine-depletion to block the growth and metastasis of methionine-dependent tumors.ПараметрыQuality Level 100, assay 99% (TLC) form powder color white mp 280 °C (dec.) (lit.) storage temp. 20°C SMILES string CCSCC[C@H](N)C(O)=O InChI 1S/C6H13NO2S/c1-2-10-4-3-5(7)6(8)9/h5H,2-4,7H2,1H3,(H,8,9)/t5-/m0/s1 InChI key GGLZPLKKBSSKCX-YFKPBYRVSA-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 -
L-Fmoc--(6-chloro-4-pyridinyl)alanine ALD00402-250MG
Empirical Formula (Hill Notation): C23H19ClN2O4 Molecular Weight: 422.86 PubChem Substance ID: 329772666 ApplicationPhenylalanine derivative was introduced in collaboration with Yu and coworkers in reflection to a methodology reported in C-H ActivationPackaging250 mg in amber glass bottleOther NotesLigand-Controlled C(sp3)–H Arylation and Olefination in Synthesis of Unnatural Chiral a–Amino Acids,ПараметрыQuality Level 100, form solid reaction suitability reaction type: Fmoc solid-phase peptide synthesis application(s) peptide synthesis: suitable functional group Fmoc storage temp. 2-8°C SMILES string O=C(O)[C@H](CC1=CC=NC(Cl)=C1)NC(OCC2C3=C(C4=C2C=CC=C4)C=CC=C3)=O InChI 1S/C23H19ClN2O4/c24-21-12-14(9-10-25-21)11-20(22(27)28)26-23(29)30-13-19-17-7-3-1-5-15(17)16-6-2-4-8-18(16)19/h1-10,12,19-20H,11,13H2,(H,26,29)(H,27,28)/t20-/m0/s1 InChI key QIUBOGQEEPYLOR-FQEVSTJZSA-N
Safety InformationRIDADR NONH for all modes of transport Узнать цену
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