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| Product | Description | |
|---|---|---|
| 1,1-Dimethoxy-2-methylpropan-2-ol | 1,1-Dimethoxy-2-methylpropan-2-ol can be synthesized from Pyruvic Aldehyde Dimethyl Acetal (P998920), a synthetic reagent used in the preparation of MCL1 inhibitors. Group: Biochemicals. Grades: Highly Purified. CAS No. 55314-33-5. Pack Sizes: 5mg, 10mg. Molecular Formula: C6H14O3, Molecular Weight: 134.169999999999. US Biological Life Sciences. |  Worldwide |
| 1-Bromo-2,4-dinitrobenzene-d3 | 1-Bromo-2,4-dinitrobenzene-d3 is an intermediate in the synthesis of dinitrophenylhydrazone (DNPH) derivatives of an aliphatic aldehyde found in mainstream cigarette smoke. Group: Biochemicals. Grades: Highly Purified. CAS No. 1313734-81-4. Pack Sizes: 100mg, 1g. Molecular Formula: C6D3BrN2O4. US Biological Life Sciences. | Worldwide |
| 2-(2-(2-Aminoethoxy)ethoxy)acetic acid | H2N-PEG2-CH2COOH belongs to a polyethylene glycol (PEG) linker covalently bound to E3 Ligase binding group (E3LB) and protein binding group (PB). H2N-PEG2-CH2COOH is a PEG derivative containing an amino group with a terminal carboxylic acid. The amino group is reactive with carboxylic acids, activated NHS esters, carbonyls (ketone, aldehyde) etc. The terminal carboxylic acid can be reacted with primary amine groups in the presence of activators (e.g. EDC, or DCC) to form a stable amide bond. PEG Linkers may be useful in the development of antibody drug conjugates and PROTACs. Synonyms: Amino-PEG2-CH2CO2H; Amino-PEG2-CH2COOH; Amino-PEG2-acetic acid. Grade: ≥95%. CAS No. 134978-97-5. Molecular formula: C6H13NO4. Mole weight: 163.17. |  |
| 2,2'-Bis(diphenylphosphino)biphenyl | 2,2'-Bis(diphenylphosphino)biphenyl. Uses: Supporting ligand in a chiral diamine-ruthenium system for the enantioselective hydrogenation of ketones. useful ligand for palladium-catalyzed amination and kumada cross-coupling reactions useful ligand for palladium-catalyzed synthesis of butatrenes. useful ligand for iridium-catalyzed c-c cross-coupling of allenes with primary alcohols via transfer hydrogenation. useful ligand for iridium-catalyzed c-c cross-coupling of dienes with primary alcohols via transfer hydrogenation. useful ligand for iridium-catalyzed c-c cross-coupling of allylic gem-dicarboxylates with aldehydes via transfer hydrogenation. useful ligand for the palladium-catalyzed synthesis of chiral allenylsilanes. ruthenium-catalyzed synthesis of indoles. ruthenium-catalyzed oxidative cyclization. rhodium-catalyzed boron arylation. Additional or Alternative Names: BIPHEP; MFCD03094574; AKOS015911364; DB-009479; 1,1'-[[1,1'-BIPHENYL]-2,2'-DIYL]BIS[1,1-DIPHENYL]-PHOSPHINE; CTK3J1519; SCHEMBL1120987; 2,2'-Bis(diphenylphosphino)biphenyl; 2,2'-bis(diphenylphosphanyl)-1,1'-biphenyl; FT-0657577. Product Category: Organic Phosphine Compounds. CAS No. 84783-64-2. Molecular formula: C36H28P2. Mole weight: 522.568g/mol. IUPACName: [2-(2-diphenylphosphanylphenyl)phenyl]-diphenylphosphane. Canonical SMILES: C1=CC=C(C=C1)P(C2=CC=CC=C2)C3=CC=CC=C3C4=CC=CC=C4P(C5=CC=CC=C5)C6=CC=CC=C6. Product ID: ACM84783642. |  |
| 2-Ethyl-2-methyl-1,3-dioxolane | 2-Ethyl-2-methyl-1,3-dioxolane is used as a reagent in the synthesis of Strychnine Hydrochloride (S687710); a compound that acts as an antagonist for cholinesterases and beta amyloid aggregation. Also used as a reagent in the study of the prodrugs of peptide aldehyde as proteasome inhibitors. Group: Biochemicals. Grades: Highly Purified. CAS No. 126-39-6. Pack Sizes: 1g, 10g. Molecular Formula: C6H12O2, Molecular Weight: 116.16. US Biological Life Sciences. | Worldwide |
| 2-Methylbutyraldehyde | 2-Methylbutyraldehyde. Group: Biochemicals. Alternative Names: α-Methylbutyraldehyde; (RS)-2-Methylbutanal; (±)-2-Methylbutanal; (±)-2-Methylbutyraldehyde; 2-Ethylpropanal; 2-Formylbutane; 2-Methylbutanal; 2-Methylbutyraldehyde; 2-Methylbutyric Aldehyde; NSC 77077; α-Methyl-n-butanal; α-Methylbutanal; α-Methylbutyraldehyde; α-Methylbutyric Aldehyde. Grades: Highly Purified. CAS No. 96-17-3. Pack Sizes: 1g. Molecular Formula: C6H12O, Molecular Weight: 100.16. US Biological Life Sciences. | Worldwide |
| 3-Methyl-3-(methylthio)butanal | 3-Methyl-3-(methylthio)butanal has been identified as one of 21 mercapto/methylthio-substituted aldehydes and ketones isolated from cooked beef liver. Group: Biochemicals. Grades: Highly Purified. CAS No. 133567-89-2. Pack Sizes: 10mg, 25mg. Molecular Formula: C6H12OS, Molecular Weight: 132.22. US Biological Life Sciences. | Worldwide |
| 3-Pyridinecarboxaldehyde-[d4] | 3-Pyridinecarboxaldehyde-[d4]. Synonyms: 3-Pyridinecarboxaldehyde D4; 3-Pyridine-2,4,5,6-d4-carboxaldehyde; Nicotinaldehyde-d4; 3-Formylpyridine-d4; 3-Pyridinaldehyde-d4; 3-Pyridylaldehyde-d4; NSC 8952-d4; Nicotinealdehyde-d4; Nicotinic aldehyde-d4; Pyridine-3-carbaldehyde-d4; Pyridine-5-carboxaldehyde-d4; Rowalind-d4; m-Formylpyridine-d4; β-Formylpyridine-d4; β-Pyridinecarbonaldehyde-d4. Grade: 95%. CAS No. 258854-80-7. Molecular formula: C6HD4NO. Mole weight: 111.13. | |
| 4,4',4'',4''',4'''',4'''''-(9,10-dihydro-9,10-[1,2]benzenoanthracene-2,3,6,7,14,15-hexayl)hexabenzaldehyde | 4,4',4'',4''',4'''',4'''''-(9,10-dihydro-9,10-[1,2]benzenoanthracene-2,3,6,7,14,15-hexayl)hexabenzaldehyde. Group: Aldehyde cof linkers-4d-aldehyder cof linkers. Alternative Names: 4-[5, 11, 12, 17, 18-pentakis(4-formylphenyl)-4-pentacyclo[6.6.6.02, 7.09, 14.015, 20]icosa-2(7), 3, 5, 9(14), 10, 12, 15(20), 16, 18-nonaenyl]benzaldehyde. CAS No. 1835723-12-0. Product ID: 4-[5, 11, 12, 17, 18-pentakis(4-formylphenyl)-4-pentacyclo[6.6.6.02, 7.09, 14.015, 20]icosa-2(7), 3, 5, 9(14), 10, 12, 15(20), 16, 18-nonaenyl]benzaldehyde. Molecular formula: 878.96. Mole weight: C62H38O6. InChI=1S/C62H38O6/c63-31-37-1-13-43 (14-2-37)49-25-55-56 (26-50 (49)44-15-3-38 (32-64)4-16-44)62-59-29-53 (47-21-9-41 (35-67)10-22-47)51 (45-17-5-39 (33-65)6-18-45)27-57 (59)61 (55)58-28-52 (46-19-7-40 (34-66)8-20-46)54 (30-60 (58)62)48-23-11-42 (36-68)12-24-48/h1-36, 61-62H. MQGKNQOUTIRYHO-UHFFFAOYSA-N. 98%. |  |
| 6-[(3R,4R)-3-(Acetyloxy)-N,4-dimethyl-6-oxo-L-norleucine] Cyclosporin A | 6-[(3R,4R)-3-(Acetyloxy)-N,4-dimethyl-6-oxo-L-norleucine] Cyclosporin A is an impurity of cyclosporin, which is a calcineurin phosphatase pathway inhibitor, used as an immunosuppressant drug to prevent rejection in organ transplantation. Synonyms: (2S,5R,8S,11S,14S,17S,20S,26S,29S,32S)-8,11,26,32-Tetraisobutyl-20-ethyl-14,29-diisopropyl-2,5,7,10,13,16,22,25,31-nonamethyl-17-[(1R,2R)-1-acetoxy-2-methyl-4-oxobutyl]-1,4,7,10,13,16,19,22,25,28,31-undecaazacyclotritriacontane-3,6,9,12,15,18,21,24,27,30,33-undecaone; Cyclosporine EP Impurity A; Cyclosporin A, 6-[(3R,4R)-3-(acetyloxy)-N,4-dimethyl-6-oxo-L-norleucine]-; Acetyl Cyclosporin A aldehyde. Grade: 98%. CAS No. 121584-52-9. Molecular formula: C62H109N11O14. Mole weight: 1232.59. | |
| 6-Aminohexanoic acid (EACA) | 6-Aminohexanoic Acid is a reagent commonly used for the extraction of aldehydes from reaction mixtures. 6-Aminohexanoic Acid has also been shown to improve solubilization of membrane proteins in electrophoresis. Studies suggest that 6-Aminohexanoic Acid inhibits the activation of the first component of the complement system.EACA is reported to inhibit chymotrypsin, Factor VIIa, lysine carboxypeptidase, plasmin, and plasminogen activator. Lysine analog. Promotes rapid dissociation of plasmin, thereby inhibiting the activation of plasminogen and subsequent fibrinolysis. Reported to inhibit plasminogen binding to activated platelets. An early report indicated that it inhibits the activation of the first component of the complement system. Binds and inactivates Carboxypeptidase B. Group: Biochemicals. Alternative Names: 6-Amino-n-hexanoic Acid; 6-Aminocaproic Acid; 6-Aminohexanoic Acid; A 14719; ACS; Acepramin; Acepramine; Acikaprin; Afibrin; Amicar; Amikar; Aminokapron; CL 10304; CY 116; Caplamin; Capramol; Caprocid; Caprolisin; EACA; EACS; Epsamon; Epsicapron; Epsikapron; Epsilcapramin; Epsilon S; Hemocaprol; Hemopar; Hepin; Ipsilon; NSC 212532; NSC 26154; NSC 400230; Respramin; ε-Amino-n-caproic. Grades: Highly Purified. CAS No. 60-32-2. Pack Sizes: 500g, 1Kg. Molecular Formula: C6H13NO2, Molecular Weight: 131.17. US Biological Life Sciences. | Worldwide |
| alcohol dehydrogenase [NAD(P)+] | Reduces aliphatic aldehydes of carbon chain length from 2 to 14, with greatest activity on C4, C6 and C8 aldehydes; also reduces retinal to retinol. Group: Enzymes. Synonyms: retinal reductase (ambiguous); aldehyde reductase (NADPH/NADH); alcohol dehydrogenase [NAD(P)]. Enzyme Commission Number: EC 1.1.1.71. CAS No. 37250-10-5. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-0355; alcohol dehydrogenase [NAD(P)+]; EC 1.1.1.71; 37250-10-5; retinal reductase (ambiguous); aldehyde reductase (NADPH/NADH); alcohol dehydrogenase [NAD(P)]. Cat No: EXWM-0355. |  |
| alcohol dehydrogenase (quinone) | Only described in acetic acid bacteria where it is involved in acetic acid production. Associated with membrane. Electron acceptor is membrane ubiquinone. A model structure suggests that, like all other quinoprotein alcohol dehydrogenases, the catalytic subunit has an 8-bladed propeller structure, a calcium ion bound to the PQQ in the active site and an unusual disulfide ring structure in close proximity to the PQQ; the catalytic subunit also has a heme c in the C-terminal domain. The enzyme has two additional subunits, one of which contains three molecules of heme c. It does not require amines for activation. It has a restricted substrate specificity, oxidizing a few primary alcohols (C2 to C6), but not methanol, secondary alcohols and some aldehydes. It is assayed with phenazine methosulfate or with ferricyanide. Group: Enzymes. Synonyms: type III ADH; membrane associated quinohaemoprotein alcohol dehydrogenase. Enzyme Commission Number: EC 1.1.5.5. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-0433; alcohol dehydrogenase (quinone); EC 1.1.5.5; type III ADH; membrane associated quinohaemoprotein alcohol dehydrogenase. Cat No: EXWM-0433. | |
| Allylpalladium(II) chloride dimer | Allylpalladium(II) chloride dimer. Uses: Precatalyst for the enantioselective hydrosilylation of olefins. precatalyst for asymmetric allylic alkylation and amination. used as a palladium source for cross-coupling reactions. can be used with trost ligands. catalyst for the carbostannylation of alkynes. used as a precatalyst for "-arylation of aldehydes. Additional or Alternative Names: Di-mu-chlorodi-pi-allyldipalladium; NSC 151255; Bis(pi-allylpalladium chloride) (VAN); MFCD00044874 (95%); Bis(mu-chloro)bis(eta3-2-propenyl)dipalladium; AK327212; 12012-95-2; Palladium, di-pi-allyldi-mu-chlorodi- (8CI); Bis((eta3-allyl)(chloro)palladium); SC10406. Product Category: Palladium series catalysts. CAS No. 12012-95-2. Molecular formula: C6H10Cl2Pd2. Mole weight: 365.886g/mol. IUPACName: chloropalladium(1+);prop-1-ene. Canonical SMILES: [CH2-]C=C.[CH2-]C=C.Cl[Pd+].Cl[Pd+]. ECNumber: 234-579-8. Product ID: ACM12012952. Alfa Chemistry ISO 9001:2015 Certified. | |
| Carbonyl(dihydrido)tris(triphenylphosphine)ruthenium(II) | Carbonyl(dihydrido)tris(triphenylphosphine)ruthenium(II). Uses: Catalyst for the arylation (or alkenylation) of anthraquinone and pbi. catalytic c-c bond formation. transfer hydrogenative coupling of isoprene to alcohols or aldehydes. alkanes (and alkenes) from alcohols by tandem hydrogen transfer and condensation. catalyst for the conversion of primary alcohols and aldehydes into methyl esters. precatalyst for hydrogen production by means of alcohol dehydrogenation. Additional or Alternative Names: 25360-32-1;Carbonyl(dihydrido)tris(triphenylphosphine)ruthenium(II);Carbonyldihydridotris(triphenylphosphine)ruthenium(II);Dihydridocarbonyltris(triphenylphosphine)ruthenium;C55H47OP3Ru;[(C6H5)3P]3Ru(CO)H2;AKOS024258165;Carbonyl(dihydrido)tris(triphenylphosphine)ruthenium (II). Product Category: Ruthenium series catalysts. CAS No. 25360-32-1. Molecular formula: C55H49OP3Ru. Mole weight: 919.987g/mol. IUPACName: formaldehyde;ruthenium dihydride;triphenylphosphane. Canonical SMILES: C=O.C1=CC=C(C=C1)P(C2=CC=CC=C2)C3=CC=CC=C3.C1=CC=C(C=C1)P(C2=CC=CC=C2)C3=CC=CC=C3.C1=CC=C(C=C1)P(C2=CC=CC=C2)C3=CC=CC=C3.[RuH2]. Product ID: ACM25360321. Alfa Chemistry ISO 9001:2015 Certified. | |
| Cinnamaldehyde | Cinnamaldehyde. Group: Biochemicals. Alternative Names: Cinnamic aldehyde; 3-Phenyl-2-propenal. Grades: Highly Purified. CAS No. 104-55-2. Pack Sizes: 1kg, 2kg, 5kg, 10kg, 25kg. Molecular Formula: C6H5CH=CHCHO. US Biological Life Sciences. | Worldwide |
| Dichloro[(S)-(-)-2,2'-bis(diphenylphosphino)-1,1'-binaphthyl]palladium(II), min. 98% | Dichloro[(S)-(-)-2,2'-bis(diphenylphosphino)-1,1'-binaphthyl]palladium(II), min. 98%. Uses: Catalyst precursor, with agbf4 , for the enantioselective addition of silyl ethers, to imines to produce β-amino ketones, and to aldehydes to produce 3-hydroxy-1-propanone aldol addition products. catalyst precursor, with agsbf6, for the asymmetric carbonyl-ene reaction. catalyst precursor for hetero diels-alder reaction of simple dienes with aldehydes and aryl glyoxals. Additional or Alternative Names: ST24050377; 5353AA; DICHLORO[2,2'-BIS(DIPHENYLPHOSPHINO)-1,1'-BINAPHTHYL]PALLADIUM(II); 115826-95-4; [(S)-(-)-2,2'-BIS(DIPHENYLPHOSPHINO)-1,1'-BINAPHTHYL]PALLADIUM (II) CHLORIDE; FT-0696081; MFCD00075254; C44H32Cl2P2Pd; EBD2199625; PALLADIUM, [1,1'-(1R)-[1,1'-BINAPHTHALENE]-2,2'-DIYLBIS[1,1-DIPHENYLPHOSPHINE-KAPPAP]]DICHLORO-, (SP-4-2)-. Product Category: Palladium series catalysts. CAS No. 127593-28-6. Molecular formula: C44H32Cl2P2Pd. Mole weight: 800.008g/mol. IUPACName: dichloropalladium;[1-(2-diphenylphosphanylnaphthalen-1-yl)naphthalen-2-yl]-diphenylphosphane. Canonical SMILES: C1=CC=C(C=C1)P(C2=CC=CC=C2)C3=C(C4=CC=CC=C4C=C3)C5=C(C=CC6=CC=CC=C65)P(C7=CC=CC=C7)C8=CC=CC=C8.Cl[Pd]Cl. Product ID: ACM127593286. Alfa Chemistry ISO 9001:2015 Certified. | |
| Furan-2,5-dicarbaldehyde | Furan-2,5-dicarbaldehyde. Group: Aldehyde cof linkers-2d-aldehyder cof linkers. Alternative Names: 2,5-Furandicarboxaldehyde. CAS No. 823-82-5. Product ID: furan-2,5-dicarbaldehyde. Molecular formula: 124.09. Mole weight: C6H4O3. InChI=1S/C6H4O3/c7-3-5-1-2-6 (4-8)9-5/h1-4H. PXJJKVNIMAZHCB-UHFFFAOYSA-N. 98%. | |
| isobutyraldoxime O-methyltransferase | Oximes of C4 to C6 aldehydes can act as acceptors; the most active substrate is 2-methylbutyroaldoxime. Group: Enzymes. Synonyms: aldoxime methyltransferase; S-adenosylmethionine:aldoxime O-methyltransferase; aldoxime O-methyltransferase. Enzyme Commission Number: EC 2.1.1.91. CAS No. 95471-32-2. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-1993; isobutyraldoxime O-methyltransferase; EC 2.1.1.91; 95471-32-2; aldoxime methyltransferase; S-adenosylmethionine:aldoxime O-methyltransferase; aldoxime O-methyltransferase. Cat No: EXWM-1993. | |
| N,N,N',N'-Tetra(4-formylphenyl)benzidin | N,N,N',N'-Tetra(4-formylphenyl)benzidin. Group: Aldehyde cof linkers-4d-aldehyder cof linkers. Alternative Names: 4, 4', 4'', 4'''- ([1, 1'-biphenyl]-4, 4'-diylbis (azanetriyl))tetrabenzaldehyde; 4- (4-Formyl-N-[4-[4- (4-formyl-N- (4-formylphenyl) anilino) phenyl]phenyl]anilino) benzaldehyde. CAS No. 865448-72-2. Product ID: 4- (4-formyl-N-[4-[4- (4-formyl-N- (4-formylphenyl) anilino) phenyl]phenyl]anilino) benzaldehyde. Molecular formula: 600.66. Mole weight: C40H28N2O4. C1=CC (=CC=C1C=O)N (C2=CC=C (C=C2)C=O)C3=CC=C (C=C3)C4=CC=C (C=C4)N (C5=CC=C (C=C5)C=O)C6=CC=C (C=C6)C=O. InChI=1S / C40H28N2O4 / c43-25-29-1-13-35 (14-2-29) 41 (36-15-3-30 (26-44) 4-16-36) 39-21-9-33 (10-22-39) 34-11-23-40 (24-12-34) 42 (37-17-5-31 (27-45) 6-18-37) 38-19-7-32 (28-46) 8-20-38 / h1-28H. HPVDCPGIWARHER-UHFFFAOYSA-N. 96%. | |
| Phloroglucinol, Hydrate, Reagent | Phloroglucinol, Hydrate, Reagent. Synonyms: Phloroglucinol dihydrate. CAS No. 6099-90-7. Pack Sizes: 25, 100 g in glass bottle. Product ID: CDC10-0062. Molecular formula: C6H3(OH)3 xH2O. Category: Antioxidant Cosmetic Chemicals. Product Keywords: Cosmetic Ingredients; Antioxidant Cosmetic Chemicals; Phloroglucinol, Hydrate, Reagent; CDC10-0062; 6099-90-7; C6H3(OH)3 xH2O; Phloroglucinol dihydrate; 203-611-2; MFCD00149090; 6099-90-7. Purity: 0.97. Color: Almost white to beige. EC Number: 203-611-2. Physical State: Solid. Quality Level: 100. Storage: Keep in dark place,Sealed in dry,Room Temperature. Application: In microscopy as a decalcifier of bone specimens. Reagent for pentoses, pentosans and aldehydes. Melting Point: 218-221 °C (A) (lit.). |  |
| pyrazine-2,5-dicarbaldehyde | pyrazine-2,5-dicarbaldehyde. Group: Aldehyde cof linkers-2d-aldehyder cof linkers. CAS No. 77666-94-5. Product ID: pyrazine-2,5-dicarbaldehyde. Molecular formula: 136.11g/mol. Mole weight: C6H4N2O2. InChI=1S/C6H4N2O2/c9-3-5-1-7-6 (4-10)2-8-5/h1-4H. HTGODBGFEKUXOL-UHFFFAOYSA-N. | |
| [RuCl(p-cymene)((S)-tolbinap)]Cl | [RuCl(p-cymene)((S)-tolbinap)]Cl. Uses: 1. useful ligand for palladium-catalyzed carbon-oxygen bond formation. 2. ligand for palladium-catalyzed α-arylation of ketones. 3. ligand for cu-catalyzed asymmetric conjugate reduction. 4. ligand for cu-catalyzed asymmetric dienolate addition to aldehydes. 5. enantioselective conjugate reduction of lactones and lactams. 6. ligand used in the enantioselective cycloaddition of allenylsilanes. Additional or Alternative Names: SC10123; (R)-RuCl[(p-cymene)(T-BINAP)]Cl; Chloro[(R)-(+)-2,2 -bis(di-p-tolylphosphino)-1; CHLORO[(S)-(-)-2,2'-BIS(DI-P-TOLYLPHOSPHINO)-1,1'-BINAPHTHYL](P-CYMENE)RUTHENIUM(II) CHLORIDE; MFCD09753014; (S)-RuCl[(p-cymene)(T-BINAP)]Cl; C58H54Cl2P2Ru. Product Category: Ruthenium series catalysts. CAS No. 228120-95-4. Molecular formula: C58H54Cl2P2Ru. Mole weight: 984.988g/mol. IUPACName: [1-[2-bis(4-methylphenyl)phosphanylnaphthalen-1-yl]naphthalen-2-yl]-bis(4-methylphenyl)phosphane;dichlororuthenium;1-methyl-4-propan-2-ylbenzene. Canonical SMILES: CC1=CC=C(C=C1)C(C)C.CC1=CC=C(C=C1)P(C2=CC=C(C=C2)C)C3=C(C4=CC=CC=C4C=C3)C5=C(C=CC6=CC=CC=C65)P(C7=CC=C(C=C7)C)C8=CC=C(C=C8)C.Cl[Ru]Cl. Product ID: ACM228120954. Alfa Chemistry ISO 9001:2015 Certified. | |
| trans-2-Hexenal | trans-2-Hexenal. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Hexenal, Leaf aldehyde, trans-2-Hexenal, Hexobarbitone, Hexobarbital, Evipan, 2-trans-Hexenal, 2-HEXENAL, trans-Hex-2-enal, 2-Hexenal, (E)-, Hexylenic aldehyde, beta-Propyl acrolein, 3-propyl acrolein, beta-Propylacrolein, Sodium hexobarbital, Hex-2-enal, 2-hexenal, E, trans-2-Hexen-1-al, Hexobarbital, Sodium, (E)-2-HEXENAL. Product Category: Heterocyclic Organic Compound. CAS No. 505-57-7. Molecular formula: C6H10O. Mole weight: 98.143000 [g/mol]. Purity: 0.96. IUPACName: (E)-hex-2-enal. Canonical SMILES: CCCC=CC=O. Density: 0.828g/cm³. ECNumber: 208-014-0. Product ID: ACM505577. Alfa Chemistry ISO 9001:2015 Certified. | |
| trans-2-Hexenal-D2 | trans-2-Hexenal-D2 is a labelled analogue of trans-2-Hexenal (H294820). trans-2-Hexenal is an unsaturated aldehyde that has an apple odour. trans-2-Hexenal is produced by soybean plants, and is also a sex pheromone produced by the female polyphemus moth. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg. Molecular Formula: C6H8D2O. US Biological Life Sciences. | Worldwide |
| trans-2-Hexenal-D4 | trans-2-Hexenal-D4 is a labelled analogue of trans-2-Hexenal (H294820). trans-2-Hexenal is an unsaturated aldehyde that has an apple odour. trans-2-Hexenal is produced by soybean plants, and is also a sex pheromone produced by the female polyphemus moth. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg, 10mg. Molecular Formula: C6H6D4O, Molecular Weight: 102.17. US Biological Life Sciences. | Worldwide |
| 2,6-Dideoxy-2-fluoro-L-mannose | 2,6-Dideoxy-2-fluoro-L-mannose, a highly regarded compound in the field of biomedicine, serves as a crucial element in the extensive study of glycoprotein biosynthesis. As an epitome of a substrate analog, it diligently mimics the enzymatic functionalities required for such processes. Imposing its significance, this compound has proven invaluable in unraveling the intricate connections between glycosylation and various ailments, encompassing cancer, diabetes, and autoimmune disorders. To procure this pivotal compound, one can readily acquire it from reputable chemical suppliers with utmost reliability. Synonyms: 2,6-dideoxy-2-fluoro-aldehydo-L-manno-hexose; L-Mannose, 2,6-dideoxy-2-fluoro-. CAS No. 74553-21-2. Molecular formula: C6H11FO4. Mole weight: 166.15. | |
| 2-Amino-2-deoxy-D-idose | 2-Amino-2-deoxy-D-idose, a rather uncommon amino sugar that is present in the cell walls of gram-negative bacteria, displays promising potential as an antibacterial agent against methicillin-resistant Staphylococcus aureus (MRSA) by impeding the production of peptidoglycan in bacterial cell walls. Further research has also investigated its potential for cancer treatment as it has exhibited the ability to hinder the growth and proliferation of cancerous cells. This compound's properties offer a comprehensive view of its potential therapeutic applications. Synonyms: 2-amino-3,4,5,6-tetrahydroxyhexanal; 2-Amino-2-deoxyhexose; 6915-39-5; 579-32-8; 7535-00-4; 72904-60-0; 14307-02-9; Galactose, 2-amino-2-deoxy-; Hexose, 2-amino-2-deoxy-; 2-Amino-2-deoxyhexose #; SCHEMBL2560773; CHEMBL4777590; DTXSID90865463; FZHXIRIBWMQPQF-UHFFFAOYSA-N; BCP30031; 3-QUINOXALIN-2-YL-ACRYLICACID; SB45341; SB45694; SY288134; FT-0624549; FT-0773918; EN300-86064; A66741BE-8D02-48CA-9ABE-AC5F6085EB5F; 2-Amino-2-deoxy-D-manno-hexose; Aldehydo-D-mannosamine. CAS No. 579-32-8. Molecular formula: C6H13NO5. Mole weight: 179.17. | |
| 3,6-Dideoxy-D-arabino-hexose | 3,6-Dideoxy-D-arabino-hexose, a remarkable and intricately designed natural sugar derivative, finds extensive utilization within the biomedical industry. This extraordinary compound serves as a fundamental cornerstone for the synthesis of a diverse array of pharmaceuticals and compounds, encompassing exceptionally vital anti-inflammatory agents and cutting-edge antiviral medications. Demonstrating its unparalleled significance, this compound exerts a pivotal role in combating infectious diseases through its exceptional ability to impede viral replication. Synonyms: Ascarylose; 3,6-dideoxy-D-mannose; aldehydo-tyvelose. CAS No. 5658-12-8. Molecular formula: C6H12O4. Mole weight: 148.16. | |
| 3,6-Dideoxy-L-arabino-hexose | 3,6-Dideoxy-L-arabino-hexose is a pivotal compound extensively utilized in the biomedical realm for its remarkable potential in combating bacteria. Its profound efficacy as an antimicrobial agent, specifically targets gram-negative bacteria. Synonyms: Ascarylose; 3,6-Dideoxy-D-arabino-hexose; 3,6-dideoxy-D-mannose; aldehydo-tyvelose; L-arabino-Hexose, 3,6-dideoxy-. CAS No. 32142-24-8. Molecular formula: C6H12O4. Mole weight: 148.16. | |
| D-Altrose | D-Altrose is a revered compound, emerging as a promising ally in studying diverse bacterial infections. Demonstrating its multifunctional attributes, it not only serves as a pivotal antibiotic precursor, stimulating their synthesis, but also augments their effectiveness. Moreover, the remarkable inhibitory prowess of D-Altrose against specific pathogenic bacteria endows it with unrivaled potential in studying the menacing antibiotic-resistant strains. Synonyms: D(+)-Altrose; Altrose, D-; aldehydo-D-altrose. CAS No. 1990-29-0. Molecular formula: C6H12O6. Mole weight: 180.16. | |
| D-Galacturonic acid | D-Galacturonic acid is a crucial component used in the biomedical industry for various applications playing a vital role in the development of drugs targeting cancer, as well as in the research of diabetes and cardiovascular diseases. This acid acts as a key intermediate in synthesizing advanced pharmaceutical compounds. Synonyms: aldehydo-D-galacturonic acid. Grade: 98%. CAS No. 685-73-4. Molecular formula: C6H10O7. Mole weight: 194.14. | |
| D(+)-Glucose | It is produced in humans via hepatic gluconeogenesis and breakdown of polymeric glucose forms (glycogenolysis). It circulates in human circulation as blood glucose and acts as an essential energy source for many organisms through aerobic or anaerobic respiration and fermentation. It is primarily stored as starch in plants and glycogen in animals to be used in various metabolic processes in the cellular level. Alternative Names: (2R,3S,4R,5R)-2,3,4,5,6-pentahydroxyhexanal. Dextrose Anhydrous. aldehydo-D-glucose. CAS No. 50-99-7. Product ID: PIPB-0123. Molecular formula: C6H12O6. Mole weight: 180.16. SMILES: C([C@@H]1[C@H]([C@@H]([C@H](C(O1)O)O)O)O)O. Appearance: Watery odorless colorless liquid. Category: Sugar Alcohols. |  |
| D-Gulose | D-Gulose is a pivotal biomedical resource, playing an eminent role in studying various metabolic disorders and diabetes. With its profound impact on energy metabolism and carbohydrate assimilation, it acts as a vital precursor in the synthesis of D-gluconic acid. Synonyms: aldehydo-D-gulose; (3R,4R,5R,6R)-6-(hydroxymethyl)oxane-2,3,4,5-tetrol. CAS No. 4205-23-6. Molecular formula: C6H12O6. Mole weight: 180.16. | |
| D-Rhamnose | D-Rhamnose is a naturally existing sugar sith multifunctional attributes encompassing anti-inflammatory and antibacterial properties. It can be used to study bacterial infections and diminish swelling affiliated with specific circumstances. Synonyms: 6-Deoxy-D-mannose; aldehydo-D-rhamnose; Isodulcite; D-Rha. CAS No. 634-74-2. Molecular formula: C6H12O5. Mole weight: 164.16. | |
| D-Talose | D-Talose, a pivotal ingredient within the biomedical sphere, showcases its exceptional value in combating an array of ailments, including diabetes and cancer. Recognized for its medicinal prowess, this extensively examined compound exhibits captivating potential in pharmaceutical progress and the amelioration of maladies. Presenting a broad scope of applications, D-Talose stands as an indispensable force propelling biomedical exploration while simultaneously heightening the likelihood of positive prognoses for patients. Synonyms: D-(+)-Talose; aldehydo-D-talose; (2S,3S,4S,5R)-2,3,4,5,6-pentahydroxyhexanal; 8ZW23G7NVD; NSC-224293; EINECS 219-996-5; TALOSE, D-; UNII-8ZW23G7NVD; SCHEMBL37336; CHEBI:68461; GZCGUPFRVQAUEE-KAZBKCHUSA-N; DTXSID701318243; GEO-04668; MFCD00135834; AKOS024256927; HY-W145492; NSC 224293; CS-0214426; T72182; A877420; Q423195; W-202099; A02CA752-AB99-4BBF-84BA-31F5846CA891. CAS No. 2595-98-4. Molecular formula: C6H12O6. Mole weight: 180.16. | |
| Glucose | A primary source of energy for living organisms. It is naturally occurring and is found in fruits and other parts of plants in its free state. It is used therapeutically in fluid and nutrient replacement. Alternative Names: D(+)-Glucose. (2R,3S,4R,5R)-2,3,4,5,6-pentahydroxyhexanal. Dextrose Anhydrous. aldehydo-D-glucose. CAS No. 58367-01-4. Product ID: CHE58367014. Molecular formula: C6H12O6. Mole weight: 180.16. SMILES: C(C(C(C(C(C=O)O)O)O)O)O. Appearance: Colorless crystals or white granular powder. Category: Food Additives. | |
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