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99 atom % 13C. Group: Magnetic resonance imaging/spectroscopy.
ethanolamine ammonia-lyase
A cobalamin protein. Group: Enzymes. Synonyms: ethanolamine deaminase. Enzyme Commission Number: EC 4.3.1.7. CAS No. 9054-69-7. 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-5294; ethanolamine ammonia-lyase; EC 4.3.1.7; 9054-69-7; ethanolamine deaminase. Cat No: EXWM-5294.
Ethanolamine hydrochloride
Ethanolamine hydrochloride. Group: Biochemicals. Alternative Names: 2-Aminoethanol hydrochloride; 2-Hydroxyethylammonium chloride. Grades: Highly Purified. CAS No. 2002-24-6. Pack Sizes: 100g. US Biological Life Sciences.
Worldwide
Ethanolamine hydrochloride
Ethanolamine hydrochloride, is an organic compound used in various industrial applications. It is a white or colorless solid that is soluble in water and has a faint odor. One of the major uses of Ethanolamine hydrochloride is in the production of detergents and surfactants. Used as a raw material in the manufacture of compounds such as ethylenediaminetetraacetic acid (EDTA) and diethanolamine, which are commonly used in household and industrial cleaning products. Ethanolamine hydrochloride is also used in the synthesis of pharmaceuticals, agrochemicals and rubber processing agents. It acts as a buffer in certain chemical reactions, helping to adjust pH and maintain stability. Ethanolamine hydrochloride can be used for gas purification and metal corrosion inhibitor. Its ability to react with acid gases such as carbon dioxide and sulfur dioxide makes it useful for removing impurities from natural gas and other industrial gases. Overall, Ethanolamine hydrochloride is a multifunctional compound with many potential industrial applications. Its ability to act as a buffer, chelating agent, and corrosion inhibitor makes it an important tool in a variety of industries. Uses: Scientific research. Group: Biochemical assay reagents. Alternative Names: 2-Aminoethanol hydrochloride. CAS No. 2002-24-6. Pack Sizes: 25 g; 50 g. Product ID: HY-W035903.
Ethanolamine hydrochloride
Ethanolamine hydrochloride. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 2-Amino-ethanohydrochloride. Product Category: Enol Ethers. Appearance: Liquid. CAS No. 2002-24-6. Molecular formula: C2H8ClNO. Mole weight: 97.54. Purity: 0.98. IUPACName: 2-Aminoethanol. Canonical SMILES: C(CO)N.Cl. Product ID: ACM2002246. Alfa Chemistry ISO 9001:2015 Certified. Categories: 2-Aminoethanol hydrochloride.
Ethanolamine hydrochloride,[1-3h]
Ethanolamine hydrochloride,[1-3h]. Uses: Designed for use in research and industrial production. Additional or Alternative Names: ETHANOLAMINE HYDROCHLORIDE, [1-3H]. Product Category: Heterocyclic Organic Compound. CAS No. 133827-62-0. Molecular formula: C2H6ClNOT2. Mole weight: 101.56. Product ID: ACM133827620. Alfa Chemistry ISO 9001:2015 Certified.
Ethanolamine hydrochloride 99+%
Ethanolamine hydrochloride 99+%. Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 25g, 100g, 250g, 1Kg, 5Kg. US Biological Life Sciences.
Worldwide
ethanolamine kinase
This enzyme belongs to the family of transferases, specifically those transferring phosphorus-containing groups (phosphotransferases) with an alcohol group as acceptor. The systematic name of this enzyme class is ATP:ethanolamine O-phosphotransferase. Other names in common use include ethanolamine kinase (phosphorylating), and ethanolamine phosphokinase. This enzyme participates in glycerophospholipid metabolism. Group: Enzymes. Synonyms: ethanolamine kinase (phosphorylating); ethanolamine phosphokinase. Enzyme Commission Number: EC 2.7.1.82. CAS No. 9075-78-9. 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-3112; ethanolamine kinase; EC 2.7.1.82; 9075-78-9; ethanolamine kinase (phosphorylating); ethanolamine phosphokinase. Cat No: EXWM-3112.
ethanolamine oxidase
A cobamide-protein. Group: Enzymes. Enzyme Commission Number: EC 1.4.3.8. CAS No. 9013-00-7. 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-1484; ethanolamine oxidase; EC 1.4.3.8; 9013-00-7. Cat No: EXWM-1484.
ethanolamine-phosphate cytidylyltransferase
This enzyme belongs to the family of transferases, specifically those transferring phosphorus-containing nucleotide groups (nucleotidyltransferases). The systematic name of this enzyme class is CTP:ethanolamine-phosphate cytidylyltransferase. Other names in common use include phosphorylethanolamine transferase, ET, CTP-phosphoethanolamine cytidylyltransferase, phosphoethanolamine cytidylyltransferase, and ethanolamine phosphate cytidylyltransferase. This enzyme participates in aminophosphonate metabolism and glycerophospholipid metabolism. Group: Enzymes. Synonyms: phosphorylethanolamine transferase; ET; CTP-phosphoethanolamine cytidylyltransferase; phosphoethanolamine cytidylyltransferase; ethanolamine phosphate cytidylyltransferase. Enzyme Commission Number: EC 2.7.7.14. CAS No. 9026-33-9. 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-3230; ethanolamine-phosphate cytidylyltransferase; EC 2.7.7.14; 9026-33-9; phosphorylethanolamine transferase; ET; CTP-phosphoethanolamine cytidylyltransferase; phosphoethanolamine cytidylyltransferase; ethanolamine phosphate cytidylyltransferase. Cat No: EXWM-3230.
ethanolamine-phosphate phospho-lyase
A pyridoxal-phosphate protein. Also acts on D(or L)-1-aminopropan-2-ol O-phosphate. Group: Enzymes. Synonyms: O-phosphoethanolamine-phospholyase; amino alcohol O-phosphate phospholyase; O-phosphorylethanol-amine phospho-lyase; ethanolamine-phosphate phospho-lyase (deaminating). Enzyme Commission Number: EC 4.2.3.2. CAS No. 37290-88-3. 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-5176; ethanolamine-phosphate phospho-lyase; EC 4.2.3.2; 37290-88-3; O-phosphoethanolamine-phospholyase; amino alcohol O-phosphate phospholyase; O-phosphorylethanol-amine phospho-lyase; ethanolamine-phosphate phospho-lyase (deaminating). Cat No: EXWM-5176.
ethanolaminephosphotransferase
This enzyme belongs to the family of transferases, specifically those transferring non-standard substituted phosphate groups. This enzyme participates in 3 metabolic pathways: aminophosphonate metabolism, glycerophospholipid metabolism, and ether lipid metabolism. Group: Enzymes. Synonyms: EPT; diacylglycerol ethanolaminephosphotransferase; CDPethanolamine diglyceride phosphotransferase; phosphorylethanolamine-glyceride transferase; CDP-ethanolamine:1,2-diacylglycerol ethanolaminephosphotransferase. Enzyme Commission Number: EC 2.7.8.1. CAS No. 9026-19-1. 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-3309; ethanolaminephosphotransferase; EC 2.7.8.1; 9026-19-1; EPT; diacylglycerol ethanolaminephosphotransferase; CDPethanolamine diglyceride phosphotransferase; phosphorylethanolamine-glyceride transferase; CDP-ethanolamine:1,2-diacylglycerol ethanolaminephosphotransferase. Cat No: EXWM-3309.
Ethanolamine SG
2.5lt Pack Size. Group: Solvents. Formula: C2H7NO. CAS No. 141-43-5. Prepack ID 69384991-2.5lt. Molecular Weight 61.08. See USA prepack pricing.
1, 2-Dioleoyl -sn-glycero-3-phosphatidyl ethanolamine-d4 is labelled 1, 2-Dioleoyl -sn-glycero-3-phosphatidyl ethanolamine (DOPE) (D482210) which is a synthetic analog of naturally-occurring PE containing 18:1 fatty acids at the sn-1 and sn-2 positions. DOPE can be used as an emulsifier to facilitate DNA-liposome complex transport across membranes. It is used in combination with cationic phospholipids to increase efficiency during DNA transfection studies as a non-viral method of gene delivery. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg. Molecular Formula: C41H74D4NO8P, Molecular Weight: 748.06. US Biological Life Sciences.
1, 2-Dioleoyl -sn-glycero-3-phosphatidyl ethanolamine (DOPE) is a synthetic analog of naturally-occurring PE containing 18:1 fatty acids at the sn-1 and sn-2 positions. DOPE can be used as an emulsifier to facilitate DNA-liposome complex transport across membranes. It is used in combination with cationic phospholipids to increase efficiency during DNA transfection studies as a non-viral method of gene delivery. Group: Biochemicals. Grades: Highly Purified. CAS No. 4004-5-1. Pack Sizes: 25mg, 100mg. Molecular Formula: C41H78NO8P, Molecular Weight: 744.03. US Biological Life Sciences.
1,2-Dipalmitoyl-sn-glycero-3-phospho-(N-methyl)-ethanolamine. CAS No: 3930-13-0
Sarchem Laboratories New Jersey NJ
Aminoethyl Ethanolamine
Aminoethyl Ethanolamine. Group: Polymers.
CDP-ethanolamine
CDP-ethanolamine, a pivotal intermediary in the biosynthesis of membrane phospholipids, assumes an indispensable function in preserving cellular membrane integrity. Clinical research evince that it ameliorates cognitive development in patients diagnosed with neurodegenerative conditions, notably Alzheimer's disease. Furthermore, it potentially mitigates glaucoma symptoms by diminishing intraocular pressure while enhancing blood flow, thereby ameliorating optic nerve functionality. Synonyms: Cytidine-5'-diphosphate ethanolamine; Cytidine-5'-diphosphateethanolamine. Grades: ≥ 95% by HPLC. CAS No. 3036-18-8. Molecular formula: C11H20N4O11P2. Mole weight: 446.25.
Ciclopirox ethanolamine
Ciclopirox ethanolamine (Ciclopirox olamine, HOE 296) is a broad-spectrum antifungal agent working as an iron chelator. Uses: Antifungal agents. Synonyms: Ciclopirox olamine; 41621-49-2; Ciclopirox ethanolamine; ciclopiroxolamine; Batrafen; Micoxolamina; Brumixol; Mycoster; Ciclopiroxolamin; Ciclochem; Dafnegin; Ciclopirox (olamine); HOE 296; Ciclopirox ethanolamine salt (1:1); HOE-296; UNII-50MD4SB4AP; EINECS 255-464-9; 50MD4SB4AP; NSC 336278; NSC-336278; DTXSID6045583; RV4104A; MFCD00078997; 6-Cyclohexyl-1-hydroxy-4-methyl-2(1H)-pyridone ethanolamine salt; Ciclobirox Olamine; 6-Cyclohexyl-1-hydroxy-4-methylpyridin-2(1H)-one compound with 2-aminoethanol (1:1); MLS003170863; 2-aminoethanol; 6-cyclohexyl-1-hydroxy-4-methylpyridin-2-one. Grades: >98%. CAS No. 41621-49-2. Molecular formula: C12H17NO2.C2H7NO. Mole weight: 268.35.
Ciclopirox Ethanolamine
Ciclopirox derivative. Broad spectrum antimycotic agent with some antibacterial activity. Group: Biochemicals. Alternative Names: 1-Hydroxy-4-methyl-6-cyclohexyl-2-pyridinone ethanolamine salt; Batrafen; Brumixol; Ciclochem; Ciclopirox Olamine; HOE 296; Loprox; Micoxolamina; Mycoster; NSC 336278; Terit. Grades: Highly Purified. CAS No. 41621-49-2. Pack Sizes: 1g, 5g. Molecular Formula: C??H??N?O?, Molecular Weight: 268.352. US Biological Life Sciences.
Worldwide
Cytidine 5'-Diphosphate Ethanolamine Disodium Salt
Cytidine 5'-Diphosphate Ethanolamine Disodium Salt is an analog of Cytidine 5'-Diphosphate with an important role in the metabolism of phospholipides. Synonyms: Cytidine 5'-(Trihydrogen Diphosphate) P'-(2-Aminoethyl) Ester Disodium Salt; Cytidine 5'-(Trihydrogen Pyrophosphate) Mono(2-aminoethyl) Ester Disodium Salt; Cytidine Pyrophosphate 2-Aminoethyl Ester Disodium Salt; CDP-Ethanolamine Disodium Salt; Cytidine 5'-Diphosphate Ethanolamine Disodium Salt; Cytidine 5'-Diphosphoethanolamine Disodium Salt; Cytidine Diphosphate Ethanolamine Disodium Salt; Cytidine Diphosphoethanolamine Disodium Salt. Grades: 95%. Molecular formula: C11H18Na2N4O11P2. Mole weight: 490.21.
2-dimethylaminoethanol appears as a clear colorless liquid with a fishlike odor. Flash point 105°F. Less dense than water. Vapors heavier than air. Toxic oxides of nitrogen produced during combustion. Used to make other chemicals.;Liquid;Liquid;COLOURLESS LIQUID WITH PUNGENT ODOUR. Group: Polymers. Product ID: 2-(dimethylamino)ethanol. Molecular formula: 89.14g/mol. Mole weight: C4H11NO;(CH3)2NCH2CH2OH;C4H11NO. CN(C)CCO. InChI=1S/C4H11NO/c1-5(2)3-4-6/h6H, 3-4H2, 1-2H3. UEEJHVSXFDXPFK-UHFFFAOYSA-N.
Glycerol 3-Phosphoethanolamine
Glycerol 3-Phosphoethanolamine is the product of a alcoholysis reaction with phosphatidylcholine and phosphatidyl ethanolamine. Group: Biochemicals. Grades: Highly Purified. CAS No. 1190-00-7. Pack Sizes: 25mg, 100mg. Molecular Formula: C5H14NO6P, Molecular Weight: 215.14. US Biological Life Sciences.
Worldwide
Glycerophospho-N-palmitoyl ethanolamine
Glycerophospho-N-palmitoyl ethanolamine. Uses: Designed for use in research and industrial production. Additional or Alternative Names: MolPort-009-019-450, Glycerophospho-N-Palmitoyl Ethanolamine, 100575-09-5. Product Category: Heterocyclic Organic Compound. Appearance: A crystalline solid. CAS No. 100575-09-5. Molecular formula: C21H44NO7P. Mole weight: 453.6. Purity: 0.96. IUPACName: 2,3-dihydroxypropyl 2-(hexadecanoylamino)ethyl hydrogen phosphate. Canonical SMILES: CCCCCCCCCCCCCCCC(=O)NCCOP(=O)(O)OCC(CO)O. Product ID: ACM100575095. Alfa Chemistry ISO 9001:2015 Certified.
L-alpha-Lysophosphatidyl ethanolamine (from egg yolk). Group: Biochemicals. Alternative Names: L-a-Lysocephalin; 3-sn-Lysophosphatidyl ethanolamine; 1-Acyl-sn-glycero-3-phospho(2-aminoethanol). Grades: Highly Purified. CAS No. 95046-40-5. Pack Sizes: 1mg, 2mg, 5mg, 10mg, 25mg. Molecular Formula: C10H22NO7P. US Biological Life Sciences.
Worldwide
lipid A phosphoethanolamine transferase
The enzyme adds one or two ethanolamine phosphate groups to lipid A giving a diphosphate, sometimes in combination with EC 2.4.2.43 (lipid IVA 4-amino-4-deoxy-L-arabinosyltransferase) giving products with 4-amino-4-deoxy-β-L-arabinose groups at the phosphates of lipid A instead of diphosphoethanolamine groups. It will also act on lipid IVA and Kdo2-lipid A. Group: Enzymes. Synonyms: lipid A PEA transferase; PmrA; LptA. Enzyme Commission Number: EC 2.7.4.30. 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-3213; lipid A phosphoethanolamine transferase; EC 2.7.4.30; lipid A PEA transferase; PmrA; LptA. Cat No: EXWM-3213.
Intermediate in the production of labeled Lapatinib. Group: Biochemicals. Alternative Names: N-(2-Hydroxyethyl)carbamic Acid Phenylmethyl Ester-13C2,15N; (2-Hydroxyethyl)carbamic Acid Benzyl Ester-13C2,15N; 2- (Benzyl oxycarbonyl amino) ethanol-13C2, 15N. Grades: Highly Purified. Pack Sizes: 500ug. US Biological Life Sciences.
Worldwide
N-Boc-ethanolamine
N-Boc-ethanolamine. Group: Biochemicals. Alternative Names: N-(2-Hydroxyethyl)carbamic Acid 1,1-Dimethylethyl Ester; 2-t-Butoxycarbonyl aminoethanol; 2- (tert-Butoxycarbonylamino) ethanol; N-(tert-Butoxycarbonyl)-2-aminoethanol. Grades: Highly Purified. CAS No. 26690-80-2. Pack Sizes: 1g. US Biological Life Sciences.
Worldwide
N-Boc-ethanolamine
N-Boc-ethanolamine. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 2-(tert-butoxycarbonylamino)ethanol; Boc-NH-(CH2)2-1-naphthylamide; (2-hydroxy-ethyl)-carbamic acid tert-butyl ester; 2-(tert-ButoxycarbonylaMino)-1-ethanol; Boc-2-aminoethanol; N-(t-butoxycarbonyl)-2-hydroxy-ethylamine; tert-Butyl (2-hydroxyethyl)carbamate; tert-Butyl N-(2-Hydroxyethyl)carbamate; 2-Boc-ethanolamine; 2-(tert-Butoxycarbonyl)ethanolamine; tert-butyl (2-hydroxyethyl)carbamate; tert-butyl N-(2-hydroxyethyl)-carbamate; boc-aminoethanol; N-(tert-Butoxycarbonyl)ethanolamine; Boc-glycinol; Boc-Gly-ol; 2-(Boc-amino)-1-ethanol; boc-ethanolamine; (2-hydroxyethyl)carbamic acid t-butyl ester; N-(2-Hydroxyethyl)carbamic Acid tert-Butyl Ester; N-Boc-ethanolamine; N-Boc-Ethanolamine. Product Category: Amino Alcohols. Appearance: clear, light yellow viscous liquid. CAS No. 26690-80-2. Molecular formula: C7H15NO3. Mole weight: 161.2. Purity: 0.98. IUPACName: TERT-BUTYL N-(2-HYDROXYETHYL)CARBAMATE. Density: 1.042. Product ID: ACM26690802. Alfa Chemistry ISO 9001:2015 Certified.
N-Boc-N-ethyl-ethanolamine
N-Boc-N-ethyl-ethanolamine. Group: Biochemicals. Alternative Names: Boc-N-Et-aminoethanol. Grades: Highly Purified. CAS No. 152192-95-5. Pack Sizes: 1g, 2g, 5g. US Biological Life Sciences.
Worldwide
N-Boc-N-ethyl-ethanolamine 99+% (HPLC)
N-Boc-N-ethyl-ethanolamine 99+% (HPLC). Group: Biochemicals. Grades: Reagent Grade. CAS No. 152192-95-5. Pack Sizes: 1g, 5g. US Biological Life Sciences.
Worldwide
N-Boc-N-methyl-ethanolamine 99+% (HPLC)
N-Boc-N-methyl-ethanolamine 99+% (HPLC). Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 1g, 5g, 25g. US Biological Life Sciences.
Worldwide
N-(gamma-Glutamyl)ethanolamine
N-(gamma-Glutamyl)ethanolamine is a derivative of glutamine. Synonyms: N-(γ-L-glutamyl)ethanolamine. CAS No. 2650-74-0. Molecular formula: C7H14N2O4. Mole weight: 190.20.
Niclosamide ethanolamine salt
Niclosamide is an oral antihelminthic drug, which has been used to treat tapeworm infection for about 50 years. Niclosamide is also used as a molluscicide for water treatment in schistosomiasis control programs. Recently, several groups have independently discovered that niclosamide is also active against cancer cells. Evidence supports that niclosamide targets multiple signaling pathways (NF-κB, Wnt/β-catenin, Notch, ROS, mTORC1, and Stat3), most of which are closely involved with cancer stem cells. Given its potential antitumor activity, clinical trials for niclosamide and its derivatives are warranted for cancer treatment. Synonyms: BAY-73; BAY-6076; Bayluscide; HL 2448; Clonitralid; Niclosamide-olamine; Niclosamidel. Grades: ≥98%. CAS No. 1420-04-8. Molecular formula: C13H8Cl2N2O4·C2H7NO. Mole weight: 388.2.
Niclosamide Ethanolamine Salt
Niclosamide Ethanolamine Salt is an ethanolamine salt of Niclosamide (N395500), which is used as an anthelmintic drug (Cestodes). Group: Biochemicals. Grades: Highly Purified. CAS No. 1420-04-8. Pack Sizes: 50mg, 100mg. Molecular Formula: C13H8Cl2N2O4; C2H7NO. US Biological Life Sciences.
Worldwide
N-(long-chain-acyl)ethanolamine deacylase
Does not act on N-acylsphingosine or N,O-diacylethanolamine. Group: Enzymes. Synonyms: N-acylethanolamine amidohydrolase; acylethanolamine amidase. Enzyme Commission Number: EC 3.5.1.60. CAS No. 99283-61-1. 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-4450; N-(long-chain-acyl)ethanolamine deacylase; EC 3.5.1.60; 99283-61-1; N-acylethanolamine amidohydrolase; acylethanolamine amidase. Cat No: EXWM-4450.
N-z-Ethanolamine
N-z-Ethanolamine. Uses: Designed for use in research and industrial production. Additional or Alternative Names: N-Z-Ethanolamine, 2-(Z-Amino)ethanol, 407909_ALDRICH, 96097_FLUKA, NSC132101, Benzyl N-(2-hydroxyethyl)carbamate, CID280458, ZINC01719541, BBV-24869503, S01-0250, 77987-49-6. Product Category: Amino Alcohols. CAS No. 77987-49-6. Molecular formula: C10H13NO3. Mole weight: 195.22. Purity: 0.96. IUPACName: benzyl N-(2-hydroxyethyl)carbamate. Canonical SMILES: C1=CC=C(C=C1)COC(=O)NCCO. Density: 1.182g/cm³. Product ID: ACM77987496. Alfa Chemistry ISO 9001:2015 Certified.
O-Arachidonoyl ethanolamine hydrochloride
O-Arachidonoyl ethanolamine hydrochloride (O-AEA) is an AEA derivative that acts as a partial antagonist of CB1 receptor and a full agonist of CB2 receptor. O-AEA produced hypothermia in the mouse and acted as an antagonist in the presence of anandamide both in vivo and in vitro. Synonyms: O-AEA hydrochloride; Arachidonic acid-(2-aminoethyl)-ester hydrochloride; Virodhamine hydrochloride; 2-aminoethyl (5Z,8Z,11Z,14Z)-icosa-5,8,11,14-tetraenoate hydrochloride. Grades: ≥98%. CAS No. 443129-35-9. Molecular formula: C22H37NO2·HCl. Mole weight: 384.
Phosphorylethanolamine
Phosphorylethanolamine is used in the synthesis of Sphingomyelin, a type of sphingolipid found in animal cell membrane. Phosphorylethanolamine participates in phospholipid metabolism. Its release can be stimulated occasionally by depolarizing stimuli. Reduction of phosphorylethanolamine levels has been observed in Alzheimer?s and Huntington?s disease. Group: Biochemicals. Alternative Names: 2-Aminoethanol 1-(Dihydrogen Phosphate); 2-Aminoethanol Dihydrogen Phosphate Ester; 2-Aminoethanol Phosphate; Phosphoric Acid 2-Aminoethyl Ester; 2-Aminoethanol O-Phosphate; 2-Aminoethyl Dihydrogen Phosphate; Colamine phosphate; Ethanolamine O-Phosphate; Mono(2-aminoethyl) phosphate; Monoaminoethyl Phosphate; NSC 254167; O-Phosphoethanolamine; O-Phosphoryl ethanolamine; Phosphoethanolamine; Phosphonoethanolamine. Grades: Highly Purified. CAS No. 1071-23-4. Pack Sizes: 10g, 25g. Molecular Formula: C2H8NO4P, Molecular Weight: 141.06. US Biological Life Sciences.
Worldwide
Phosphorylethanolamine-d4
Labeled analogue of Phosphoryl ethanolamine. Phosphorylethanolamine is used in the synthesis of Sphingomyelin, a type of sphingolipid found in animal cell membrane. Group: Biochemicals. Alternative Names: 2-Aminoethanol-d4 1-(Dihydrogen Phosphate); 2-Aminoethanol-d4 Dihydrogen Phosphate Ester; 2-Aminoethanol-d4 Phosphate; Phosphoric Acid 2-Aminoethy-d4 Ester; 2-Aminoethanol-d4 O-Phosphate2-Aminoethyl-d4 Dihydrogen Phosphate; Colamine phosphate; Ethanolamine-d4 O-Phosphate; Mono(2-aminoethyl-d4) phosphate; Monoaminoethyl-d4 Phosphate; NSC 254167-d4; O-Phosphoethanolamine-d4; O-Phosphorylethanolamine-d4; Phosphoethanolamine-d4; Phosphonoethanolamine-d4. Grades: Highly Purified. CAS No. 1169692-38-9. Pack Sizes: 1mg. US Biological Life Sciences.
Worldwide
serine-ethanolaminephosphate phosphodiesterase
Acts only on those phosphodiesters that have ethanolamine as a component part of the molecule. Group: Enzymes. Synonyms: serine ethanolamine phosphodiester phosphodiesterase; SEP diesterase. Enzyme Commission Number: EC 3.1.4.13. CAS No. 37288-20-3. 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-3713; serine-ethanolaminephosphate phosphodiesterase; EC 3.1.4.13; 37288-20-3; serine ethanolamine phosphodiester phosphodiesterase; SEP diesterase. Cat No: EXWM-3713.
serine-phosphoethanolamine synthase
This enzyme belongs to the family of transferases, specifically those transferring non-standard substituted phosphate groups. This enzyme participates in glycerophospholipid metabolism. Group: Enzymes. Synonyms: serine ethanolamine phosphate synthetase; serine ethanolamine phosphodiester synthase; serine ethanolaminephosphotransferase; serine-phosphinico-ethanolamine synthase; serinephosphoethanolamine synthase. Enzyme Commission Number: EC 2.7.8.4. CAS No. 9023-23-8. 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-3339; serine-phosphoethanolamine synthase; EC 2.7.8.4; 9023-23-8; serine ethanolamine phosphate synthetase; serine ethanolamine phosphodiester synthase; serine ethanolaminephosphotransferase; serine-phosphinico-ethanolamine synthase; serinephosphoethanolamine synthase. Cat No: EXWM-3339.
2-[(1-Methylheptyl)amino]ethanol
2-[(1-Methylheptyl)amino]ethanol. Uses: Designed for use in research and industrial production. Additional or Alternative Names: N-2-Octylethanolamine, MolPort-001-790-148, NSC111949, 2-((1-Methylheptyl)amino)ethanol, CID98354, Ethanol, 2-[(1-methylheptyl)amino]-, EINECS 247-764-3, N-(1-METHYLHEPTYL)ETHANOLAMINE, Ethanol, 2-((1-methylheptyl)amino)-, 26535-68-2. Product Category: Heterocyclic Organic Compound. CAS No. 26535-68-2. Molecular formula: C10H23NO. Mole weight: 173.3. Purity: 0.96. IUPACName: 2-(octan-2-ylamino)ethanol. Canonical SMILES: CCCCCCC(C)NCCO. Density: 0.865g/cm³. ECNumber: 247-764-3. Product ID: ACM26535682. Alfa Chemistry ISO 9001:2015 Certified.
2- (2-Aminoethylamino) ethanol
2- (2-Aminoethylamino) ethanol is a reagent used in the synthesis of various pharmacologically active compounds and functional groups. Its used in the synthesis of antitumor anthracene-diones and antitumor DNA intercalators. More recently used in the synthesis of ionic liquids with various thermal, dielectric and catalytic properties. Group: Biochemicals. Alternative Names: (2-Hydroxyethyl) ethylenediamine; ( β -Hydroxyethyl) ethylenediamine; 1-(2-Hydroxyethylamino)-2-aminoethane; 1-Aminooxyethylamine; Amino Alcohol EA; Aminoethyl ethanolamine; N-(2-Hydroxyethyl)-1,2-diaminoethane; N-(2-Hydroxyethyl)-1,2-ethanediamine; NSC 461. Grades: Highly Purified. CAS No. 111-41-1. Pack Sizes: 10g. US Biological Life Sciences.
Worldwide
2-[ (2-Chloroacetyl) amino]ethyl 2-Chloroacetate
2-[ (2-Chloroacetyl) amino]ethyl 2-Chloroacetate is an analog of N-bromoacetyl ethanolamine phosphate as an inhibitor of tumor cell growth. Group: Biochemicals. Grades: Highly Purified. CAS No. 60945-04-2. Pack Sizes: 1g, 10g. Molecular Formula: C6H9Cl2NO3, Molecular Weight: 214.05. US Biological Life Sciences.
Worldwide
2-Aminoethan-1,1,2,2-d4-ol
2-Amino-ethan-1,1,2,2-d4-ol is labelled Ethanolamine (E676500) which is used in the preparation of various pharmaceutical compounds and inhibitors. Substituted carboxamides are synthesized using Ethanolamine that show potent antitumor activity. Also used in the synthesis of aminoquinolones which display anti-plasmodial activity. Group: Biochemicals. Grades: Highly Purified. CAS No. 85047-08-1. Pack Sizes: 25mg, 100mg. Molecular Formula: C2H3D4NO. US Biological Life Sciences.
Worldwide
2-Aminoethyl oleate
2-Aminoethyl oleate. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Ethamolin, 2-Aminoethyl oleate, ETHANOLAMINE OLEATE, Oleic acid, 2-aminoethyl ester, C20H39NO2, EINECS 221-924-2, Ethanol, 2-amino-, oleate (ester), CID6436599, 9-Octadecenoic acid (9Z)-, 2-aminoethyl ester, LS-174393, 3282-75-5. Product Category: Heterocyclic Organic Compound. CAS No. 3282-75-5. Molecular formula: C20H39NO2. Mole weight: 325.529160 [g/mol]. Purity: 0.96. IUPACName: 2-aminoethyl (Z)-octadec-9-enoate. Density: 0.905g/cm³. Product ID: ACM3282755. Alfa Chemistry ISO 9001:2015 Certified.
An ethanolamine analog used in the study of phospholipid metabolism in Tetrahymena. Synonyms: 1-Propanol, 3-amino-; 1,3-Propanolamine; 1-Amino-3-hydroxypropane; 1-Amino-3-propanol; 3-Aminopropanol; 3-Aminopropyl alcohol; 3-Hydroxy-1-aminopropane; 3-Hydroxy-1-propylamine; 3-Hydroxypropan-1-amine; 3-Hydroxypropylamine; 3-Propanolamine; N-(3-Hydroxypropyl)amine; NSC 7766; Propanolamine; β-Alaninol; γ-Aminopropanol; γ-Hydroxy-1-propylamine. Grades: ≥95%. CAS No. 156-87-6. Molecular formula: C3H9NO. Mole weight: 75.11.
4-Methoxy-1-naphthoic Acid
Used in the preparation of α-aryl/pyridinyl ethanolamines as selective β3 adrenergic receptor agonists. Group: Biochemicals. Alternative Names: 4-Methoxy-1-naphthalenecarboxylic Acid; 4-Methoxy-1-naphthoic Acid; 4-Methoxy-α-naphthoic Acid. Grades: Highly Purified. CAS No. 13041-62-8. Pack Sizes: 100mg. US Biological Life Sciences.
Worldwide
5-phosphonooxy-L-lysine phospho-lyase
A pyridoxal-phosphate protein. Has no activity with phosphoethanolamine (cf. EC 4.2.3.2, ethanolamine-phosphate phospho-lyase). Group: Enzymes. Synonyms: 5-phosphohydroxy-L-lysine ammoniophospholyase; AGXT2L2 (gene name). Enzyme Commission Number: EC 4.2.3.134. 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-5148; 5-phosphonooxy-L-lysine phospho-lyase; EC 4.2.3.134; 5-phosphohydroxy-L-lysine ammoniophospholyase; AGXT2L2 (gene name). Cat No: EXWM-5148.
This enzyme belongs to the family of transferases, specifically those acyltransferases transferring groups other than aminoacyl groups. This enzyme participates in glycerophospholipid metabolism. Group: Enzymes. Synonyms: acyl-[acyl-carrier protein]:O-(2-acyl-sn-glycero-3-phospho)-ethanolamine O-acyltransferase. Enzyme Commission Number: EC 2.3.1.40. CAS No. 37257-18-4. 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-2219; acyl-[acyl-carrier-protein]-phospholipid O-acyltransferase; EC 2.3.1.40; 37257-18-4; acyl-[acyl-carrier protein]:O-(2-acyl-sn-glycero-3-phospho)-ethanolamine O-acyltransferase. Cat No: EXWM-2219.
Boc-β-Alaninol
A reagent used in the synthesis of phosphatidyl ethanolamines and ornithine. Synonyms: tert-Butyl N-(3-hydroxypropyl)carbamate; tert-Butyl N-(3-hydroxypropyl)carbamate; N-tert-Butyloxycarbonyl-3-hydroxy-propylamine; 3-(Boc-amino)-1-propanol. Grades: ≥ 99 % (TLC). CAS No. 58885-58-8. Molecular formula: C8H17NO3. Mole weight: 175.2.
Boc-Glycinol
A reagent used in the synthesis of phosphatidyl ethanolamines and ornithine. Synonyms: 2-(Boc-amino)-ethanol; Boc-ethanolamine; N-Boc-ethanolamine; tert-Butyl N-(2-hydroxyethyl)carbamate; tert-butyl (2-hydroxyethyl)carbamate. Grades: ≥ 97 % (Assay). CAS No. 26690-80-2. Molecular formula: C7H15NO3. Mole weight: 161.2.
Cephaeline
Cephaeline is a phenolic alkaloid in Indian Ipecac roots. Cephaeline exhibits potent inhibition of both Zika virus (ZIKV) and Ebola virus (EBOV) infections. Uses: Designed for use in research and industrial production. Additional or Alternative Names: cephaeline;O-Phosphatidyl-ethanolamine;Cefalin;(-)-Cephaelin;(1R)-1-[[(2S,3R,11bS)-3-Ethyl-1,3,4,6,7,11b-hexahydro-9,10-dimethoxy-2H-benzo[a]quinolizin-2-yl]methyl]-1,2,3,4-tetrahydro-7-methoxy-6-isoquinolinol;7,10,11-Trimethoxyemetan-6-ol;Cepheline;Desmethylemetine. Product Category: Inhibitors. Appearance: Off-White to Pale Yellow Solid. CAS No. 483-17-0. Molecular formula: C28H38N2O4. Mole weight: 466.61232. Purity: 0.9841. Canonical SMILES: OC1=CC2=C([C@@H](C[C@@H]3[C@@H](CC)CN4CCC5=CC(OC)=C(OC)C=C5[C@]4([H])C3)NCC2)C=C1OC. Density: 1.21±0.1 g/cm³ (20 ºC 760 Torr). Product ID: ACM483170. Alfa Chemistry ISO 9001:2015 Certified.
choline kinase
Ethanolamine and its methyl and ethyl derivatives can also act as acceptors. Group: Enzymes. Synonyms: choline kinase (phosphorylating); choline phosphokinase; choline-ethanolamine kinase. Enzyme Commission Number: EC 2.7.1.32. CAS No. 9026-67-9. 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-3063; choline kinase; EC 2.7.1.32; 9026-67-9; choline kinase (phosphorylating); choline phosphokinase; choline-ethanolamine kinase. Cat No: EXWM-3063.
Choline Kinase (Crude Enzyme)
Choline kinase (also known as CK,ChoK and choline phosphokinase) is an enzyme which catalyzes the first reaction in the choline pathway for phosphatidylcholine (PC) biosynthesis. This reaction involves the transfer of a phosphate group from adenosine triphosphate (ATP) to choline in order to form phosphocholine. Thus, the two substrates of this enzyme are ATP and choline, whereas its two products are adenosine diphosphate (ADP) and O-phosphocholine. Choline kinase requires magnesium ions (+2) as a cofactor for this reaction. This enzyme belongs to the family of transferases, specifically those transferring phosphorus-containing groups (phosphotransferases) with an alcohol grou... CHKA and CHKB and are only active in their homodimeric, heterodimeric and oligomeric forms. This product with the indicated enzyme activity was briefly purified from engineered E. coli. Applications: Biotechnology; diagnostics; drug development; medicine. Group: Enzymes. Synonyms: Choline Kinase (phosphorylating); choline phosphokinase; choline-ethanolamine kinase. Enzyme Commission Number: EC 2.7.1.32. CAS No. 9026-67-9. Activity: Undetermined. Appearance: Clear to translucent yellow solution. Storage: at -20 °C or lower, for at least 1 month. Source: E. coli. Choline Kinase (phosphorylating); choline phosphokinase; choline-ethanolamine kinase. Pack: 100ml. Cat No: NATE-1825.
Ciclopirox olamine
Ciclopirox olamine (Ciclopirox ethanolamine) is a synthetic and orally active antifungal agent that can be used for superficial mycoses reseaech. Ciclopirox olamine has a very broad spectrum of activity and inhibits dermatophytes , yeasts , molds , and many Gram-positive and Gram-negative species pathogenic. Ciclopirox olamine also has anticancer and anti-inflammatory effect [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Ciclopirox ethanolamine; HOE 296. CAS No. 41621-49-2. Pack Sizes: 10 mM * 1 mL; 50 mg; 100 mg. Product ID: HY-B0450A.
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