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(R)-3-Hydroxybutyric acid, characterized by its role in energy metabolism, serves as a biomarker for metabolic disorders such as diabetes. In addition, it exhibits therapeutic potential in the management of neurodegenerative diseases like Alzheimer's and Parkinson's, highlighting its significance in biomedical research and clinical applications. Synonyms: (R)-3-Hydroxybutanoic acid; (R)-3-Hydroxybutanoate. Grades: 95%. CAS No. 625-72-9. Molecular formula: C4H8O3. Mole weight: 104.1.
4-Amino-3-hydroxybutyric acid
4-Amino-3-Hydroxybutanoic Acid is used as a chiral reagent in the synthesis of antiepileptic and hypotensive drug GABOB and analogs. Also used in the preparation of HIV-1 inhibitors derived from Betulinic Acid. Synonyms: 4-Amino-3-hydroxybutanoic acid; Gabob; DL-4-Amino-3-hydroxybutyric acid; 3-Hydroxy-GABA; Gabomade; Gamibetal; Gaboril; Gamma-amino-beta-hydroxybutyric acid; Buksamin; Gabimex; Gaminal; Idramina; Bogil. Grades: ≥ 99% (Assay). CAS No. 924-49-2. Molecular formula: C4H9NO3. Mole weight: 119.12.
4-Amino-3-hydroxybutyric acid
4-Amino-3-hydroxybutyric acid. Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 5g, 25g, 100g, 250g. US Biological Life Sciences.
Worldwide
DL-3-Hydroxybutyric acid sodium salt 99+%
DL-3-Hydroxybutyric acid sodium salt 99+%. Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 100g, 250g, 25g, 5g. US Biological Life Sciences.
Worldwide
Poly[(R)-3-hydroxybutyric acid]
Biocompatible, biodegradable polymer. Uses: Poly[(r)-3-hydroxybutyric acid (phb) is a biodegradable and biocompatible polymer produced by several bacterial species, owing to its low resorbability and tunable properties, it may find uses in a variety of applications such as tissue engineering, controlled release systems etc. Group: Biodegradable polymers. Alternative Names: PHB, (R)-3-Hydroxybutyric acid polymerized. CAS No. 29435-48-1. Pack Sizes: 10, 100 g in poly bottle. Product ID: [4-oxo-4-(4-oxobutan-2-yloxy)butan-2-yl] 3-hydroxybutanoate. Molecular formula: 260.28g/mol. Mole weight: [COCH2CH(CH3)O]n. CC(O)CC(O)=O. InChI=1S/C12H20O6/c1-8 (14)6-11 (15)18-10 (3)7-12 (16)17-9 (2)4-5-13/h5, 8-10, 14H, 4, 6-7H2, 1-3H3. QLACRIKFZRFWRU-UHFFFAOYSA-N.
Poly[(R)-3-hydroxybutyric acid]
natural origin. Group: Biodegradable polymers.
(R)-(-)-3-Hydroxybutyric acid ethyl ester
(R)-(-)-3-Hydroxybutyric acid ethyl ester. Group: Biochemicals. Grades: Highly Purified. CAS No. 24915-95-5. Pack Sizes: 50g, 100g, 250g, 500g, 1kg. Molecular Formula: C6H12O3. US Biological Life Sciences.
Worldwide
(R)-(-)-3-Hydroxybutyric acid, sodium salt
chiral synthon. CAS No. 13613-65-5. Product ID: 1-01138. Molecular formula: C4H7O3Na. Mole weight: 126.09. Purity: ee 99%. Properties: mp 165-167°C. Reference: J. Med. Chem.; 42, 2318, 1999; Helv. Chem. Acta, 69, 1147, 1986; J. Am. Chem. Soc., 110, 4769, 1988.
(R)-4-Amino-3-hydroxybutyric acid
(R)-4-Amino-3-hydroxybutyric acid ((R)-GABOB) is a 4-aminobutyric acids ( GABAB ) agonist. (R)-4-Amino-3-hydroxybutyric acid is promising for research of nervous disorders [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: (-)-γ-Amino-β-hydroxybutyric acid; (R)-GABOB; (-)-β-Hydroxy-GABA. CAS No. 7013-7-2. Pack Sizes: 100 mg; 250 mg; 500 mg; 1 g; 5 g. Product ID: HY-W005749.
(Rs)-4,4,4-trifluoro-3-hydroxybutyric acid. Uses: Designed for use in research and industrial production. Additional or Alternative Names: (RS)-4,4,4-TRIFLUORO-3-HYDROXYBUTYRIC ACID. Product Category: Heterocyclic Organic Compound. CAS No. 86884-21-1. Molecular formula: C4H5F3O3. Mole weight: 158.075910 [g/mol]. Purity: 0.96. IUPACName: 4,4,4-trifluoro-3-hydroxybutanoic acid. Canonical SMILES: C(C(C(F)(F)F)O)C(=O)O. Product ID: ACM86884211. Alfa Chemistry ISO 9001:2015 Certified.
Z-DL-4-amino-3-hydroxybutyric acid
Z-DL-4-amino-3-hydroxybutyric acid. Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 1g, 5g, 25g. US Biological Life Sciences.
1H-Imidazole,5-(4-ethoxyphenyl)-2-[2-(2-furanyl)ethenyl]-4-phenyl-. Uses: Designed for use in research and industrial production. Additional or Alternative Names: ETHYL-(R)-(+)-BROMO-3-HYDROXYBUTANOATE;ETHYL (R)-4-BROMO-3-HYDROXYBUTANOATE;ETHYL R-(+)-4-BROMO-3-HYDROXYBUTANOATE;ETHYL (R)-(+)-4-BROMO-3-HYDROXYBUTYRATE;BUTANOIC ACID, 4-BROMO-3-HDROXY-, ETHYL ESTER, (R);(R)-4-BROMO-3-HYDROXYBUTYRIC ACID ETHYL ETHER. Product Category: Heterocyclic Organic Compound. CAS No. 95310-48-8. Molecular formula: C23H20N2O2. Mole weight: 211.05. Purity: 0.98. IUPACName: ethyl (3R)-4-bromo-3-hydroxybutanoate. Density: 1.468 g/mL at 25 °C(lit.). Product ID: ACM95310488. Alfa Chemistry ISO 9001:2015 Certified.
(3R)-4-Cyano-3-hydroxybutanoic Acid Ethyl Ester
(3R)-4-Cyano-3-hydroxybutanoic Acid Ethyl Ester is used in a biocatalytic process for the synthesis of an atorvastatin intermediate and degredation products/impurities. Group: Biochemicals. Alternative Names: (3R)-4-Cyano-3-hydroxybutyric Acid Ethyl Ester; (R)-4-Cyano-3-hydroxybutyric Acid Ethyl Ester; (R)-Ethyl 4-Cyano-3-hydroxybutanoate; (R)-Ethyl 4-Cyano-3-hydroxybutanoate; Ethyl (R)-4-Cyano-3-hydroxybutanoate; Ethyl (R)-4-Cyano-3-hydroxybutyrate. Grades: Highly Purified. CAS No. 141942-85-0. Pack Sizes: 5g. US Biological Life Sciences.
Poly(3-hydroxybutyrate-co-3-hydroxyvalerate). Uses: Designed for use in research and industrial production. Additional or Alternative Names: POLY(3-HYDROXYBUTYRATE-CO-3-HYDROXYVALERATE);POLY(3-HYDROXYBUTYRIC ACID-CO-3-HYDROXYVALERIC ACID);copolymer of (R)-3-hydroxybutyric acid + -valeric acid (9:1);copolymer of (R)-3-hydroxybutyric acid + -valeric acid 7/3;POLY(3-HYDROXYBUTYRIC ACID-CO-3-HYDRO. Product Category: Biomaterials. CAS No. 80181-31-3. Molecular formula: C27H42O12X2. Mole weight: 558.62. Purity: 0.98. IUPACName: 3-hydroxybutanoic acid; 3-hydroxypentanoic acid. Product ID: ACM80181313. Alfa Chemistry ISO 9001:2015 Certified.
(R)-3-Hydroxybutanoic acid
(R)-3-Hydroxybutanoic acid is a metabolite, and converted from acetoacetic acid catalyzed by 3-hydroxybutyrate dehydrogenase. (R)-3-Hydroxybutanoic acid has applications as a nutrition source and as a precursor for vitamins, antibiotics and pheromones [1] [2]. Uses: Scientific research. Group: Natural products. Alternative Names: (R)-(-)-3-Hydroxybutanoic acid; (R)-3-Hydroxybutyric acid. CAS No. 625-72-9. Pack Sizes: 10 mM * 1 mL; 50 mg; 100 mg. Product ID: HY-W051723.
(R)-3-Hydroxybutanoic acid sodium
(R)-3-Hydroxybutanoic acid ((R)-3-Hydroxybutyric acid) sodium is a metabolite converted from acetoacetic acid catalyzed by 3-hydroxybutyrate dehydrogenase. (R)-3-Hydroxybutanoic acid sodium can function as a nutrition source, and as a precursor for vitamins, antibiotics and pheromones [1] [2]. Uses: Scientific research. Group: Natural products. Alternative Names: (R)-(-)-3-Hydroxybutanoic acid sodium; (R)-3-Hydroxybutyric acid sodium. CAS No. 13613-65-5. Pack Sizes: 10 mM * 1 mL; 500 mg; 1 g. Product ID: HY-W015851.
(R)-ethyl 4-cyano-3-hydroxybutanoate
(R)-ethyl 4-cyano-3-hydroxybutanoate is the impuritiy of Atorvastatin, a selective, competitive HMG-CoA reductase inhibitor. Synonyms: (3R)-4-Cyano-3-hydroxybutyric Acid Ethyl Ester; (R)-4-Cyano-3-hydroxybutyric Acid Ethyl Ester; Ethyl (R)-4-Cyano-3-hydroxybutanoate. CAS No. 141942-85-0. Molecular formula: C7H11NO3. Mole weight: 157.17.
(S)-3-Hydroxybutanoic acid
(S)-3-Hydroxybutanoic acid is a normal human metabolite, that has been found elevated in geriatric patients remitting from depression. In humans, 3-Hydroxybutyric acid is synthesized in the liver from acetyl-CoA, and can be used as an energy source by the brain when blood glucose is low. Uses: Scientific research. Group: Natural products. Alternative Names: (S)-β-Hydroxybutanoic acid; L-(+)-3-Hydroxybutyric acid; L-β-Hydroxybutyric acid. CAS No. 6168-83-8. Pack Sizes: 10 mM * 1 mL; 50 mg; 100 mg; 500 mg. Product ID: HY-W050031.
(S)-Methyl 4-cloro-3-hydroxybutyrate
(S)-Methyl 4-cloro-3-hydroxybutyrate. Uses: Designed for use in research and industrial production. Additional or Alternative Names: (S)4-Chloro-3-hydroxybutyric acid methyl ester;Methyl (S)-4-chloro-3-hydroxybutyrate;S-Methyl 4-chloro-3-hydroxybutyrate. Product Category: Heterocyclic Organic Compound. CAS No. 86728-93-0. Molecular formula: C5H9ClO3. Mole weight: 152.58. Product ID: ACM86728930. Alfa Chemistry ISO 9001:2015 Certified.
Threonine
Threonine was isolated and identified by W. C. ose in 1935 from the hydrolysate of fibrin. It has been proved to be the last essential amino acid to be discovered. It is the second or third limiting amino acid in livestock and poultry, and it has extremely important physiological functions in animals. Synonyms: L-2-AMINO-3-HYDROXYBUTANOIC ACID;L-2-AMINO-3-HYDROXYBUTYRIC ACID;L-THR;L(-)-THREONINE;L-THREONINE;H-L-THR-OH;H-THR-OH;H-THR-OH-THREONINE. CAS No. 72-19-5. Product ID: PAP-0036. Molecular formula: C4H9NO3. Category: Amino acid. Product Keywords: Amino Acid Series; Threonine; PAP-0036; Amino acid; C4H9NO3; 72-19-5. Appearance: ADML-Threonineisahighqualityproductspecif ically designedforthefeedindustry. P roducedfromadvancedtechnology, ADML-ThreonineiscChemicalbookomposedof100 % isomerically pureL-Threonine, whichtranslatesinto100% b ioavailabilityforswine, poultry, and otheranimals. mildsavory. Chemical Name: L-Threonine. Grade: Pharmaceutical Grade. Commonly used amount and the maximum amount: Accounts for 5.0% of the total protein mass in foods (FDA, § 172.320, 2000). Solubility: H2O: 50 mg/mL. Storage: 2-8°C. Applications: L-threonine is an essential amino acid, widely used in medicine, food, animal feed and so on. Boiling Point: 222.38°C (rough estimate). Melting Point: 256 °C (dec.) (lit.). Density: 1.3126 (rough estimate). Product Description: Threonine is an essential amino acid, mainly used as a nutritional supplement, oft
Butanoic acid,4-bromo-3-hydroxy-,ethyl ester,(3S)-. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 479608_ALDRICH, ZINC02567774, CID2733694, Ethyl (S)-(-)-4-bromo-3-hydroxybutyrate, 95537-36-3. Product Category: Heterocyclic Organic Compound. Appearance: clear yellow liquid. CAS No. 95537-36-3. Molecular formula: C6H11BrO3. Mole weight: 211.0537. Purity: N/A. IUPACName: ethyl (3S)-4-bromo-3-hydroxybutanoate. Canonical SMILES: CCOC(=O)CC(CBr)O. Density: 1.468 g/mL at 25ºC(lit.). ECNumber: 619-147-2. Product ID: ACM95537363. Alfa Chemistry ISO 9001:2015 Certified.
D-3-hydroxybutyrate dehydrogenase from Microorganism
In enzymology, a 3-hydroxybutyrate dehydrogenase (EC 1.1.1.30) is an enzyme that catalyzes the chemical reaction: (R)-3-hydroxybutanoate + NAD+ ? acetoacetate + NADH + H+. Thus, the two substrates of this enzyme are (R)-3-hydroxybutanoate and NAD+, whereas its three products are acetoacetate, NADH, and H+. This enzyme belongs to the family of oxidoreductases, to be specific, those acting on the CH-OH group of donor with NAD+ or NADP+ as acceptor. This enzyme participates in synthesis and degradation of ketone bodies and butanoate metabolism. Group: Enzymes. Synonyms: (R)-3-hydroxybutanoate: NAD+ oxidoreductase; NAD+-beta-hydroxybutyrate dehydro. Enzyme Commission Number: EC 1.1.1.30. CAS No. 9028-38-0. Mole weight: 27.5 kDa (SDS-PAGE). Activity: >300U/mg. Storage: Store at -20°C. Form: Yellowish powder, lyophilized. Source: Microorganism. (R)-3-hydroxybutanoate: NAD+ oxidoreductase; NAD+-beta-hydroxybutyrate dehydrogenase; hydroxybutyrate oxidoreductase; beta-hydroxybutyrate dehydrogenase; D-beta-hydroxybutyrate dehydrogenase; D-3-hydroxybutyrate dehydrogenase; D-( - )-3-hydroxybutyrate dehydrogenase; beta-hydroxybutyric acid dehydrogenase; 3-D-hydroxybutyrate dehydrogenase; beta-hydroxybutyric dehydrogenase; EC 1.1.1.30; 9028-38-0; HBDH; β-Hydroxybutyrate Dehydrogenase; 3-Hydroxybutyrate Dehydrogenase. Cat No: NATE-1714.
In mammalian systems, β-hydroxybutyrate dehydrogenase is localized on the inner mitochondrial membrane and requires phosphatidyl choline for activity. In contrast, the enzyme from Pseudomonas is a soluble cytosolic enzyme that does not require a phospholipid allosteric activator. The enzyme is required for the utilization of ketone bodies as a source of metabolic energy. It catalyzes the oxidation of 3-hydroxybutyrate to acetoacetate, the first step in the conversion of ketone bodies to citric acid, which is then further metabolized via the tricarboxylic acid cycle (Krebs cycle). Is an enzyme produced by microorganisms. this product shall be used for a diag...Enzyme Commission Number: EC 1.1.1.30. CAS No. 9028-38-0. 3-HBDH. Mole weight: 60±5 kDa (TSK G-3000SW); 30±5 kDa (SDS-PAGE). Activity: > 1,500 U/mg. Appearance: White powder. Storage: -20°C. Form: Freeze dried powder. Source: Alcaligenes faecalis. 3-hydroxybutyrate dehydrogenase; 3-HBDH; NAD-β-hydroxybutyRate dehydrogenase; hydroxybutyRate oxidoreductase; β-hydroxybutyRate dehydrogenase; D-β-hydroxybutyRate dehydrogenase; D-3-hydroxybutyRate dehydrogenase; D-(-)-3-hydroxybutyRate dehydrogenase; β-hydroxybutyric acid dehydrogenase; 3-D-hydroxybutyRate dehydrogenase; β-hydroxybutyric dehydrogenase; EC 1.1.1.30; 9028-38-0. Cat No: NATE-0005.
In mammalian systems, β-hydroxybutyrate dehydrogenase is localized on the inner mitochondrial membrane and requires phosphatidyl choline for activity. In contrast, the enzyme from Pseudomonas is a soluble cytosolic enzyme that does not require a phospholipid allosteric activator. The enzyme is required for the utilization of ketone bodies as a source of metabolic energy. It catalyzes the oxidation of 3-hydroxybutyrate to acetoacetate, the first step in the conversion of ketone bodies to citric acid, which is then further metabolized via the tricarboxylic acid cycle (Krebs cycle). Applications: Suitable for the determination of acetoacetate and d (-)-3-hy...1.1.30; 9028-38-0. Enzyme Commission Number: EC 1.1.1.30. CAS No. 9028-38-0. 3-HBDH. Activity: > 200 units/mg protein. Storage: -20°C. Form: Lyophilized powder containing sucrose, β-NAD and Tris buffer salts. Source: Pseudomonas lemoignei. 3-hydroxybutyrate dehydrogenase; 3-HBDH; NAD-β-hydroxybutyRate dehydrogenase; hydroxybutyRate oxidoreductase; β-hydroxybutyRate dehydrogenase; D-β-hydroxybutyRate dehydrogenase; D-3-hydroxybutyRate dehydrogenase; D-(-)-3-hydroxybutyRate dehydrogenase; β-hydroxybutyric acid dehydrogenase; 3-D-hydroxybutyRate dehydrogenase; β-hydroxybutyric dehydrogenase; EC 1.1.1.30; 9028-38-0. Cat No: NATE-0003.
In enzymology, a 3-hydroxybutyrate dehydrogenase (EC 1.1.1.30) is an enzyme that catalyzes the chemical reaction: (R)-3-hydroxybutanoate + NAD+ <-> acetoacetate + NADH + H+. Thus, the two substrates of this enzyme are (R)-3-hydroxybutanoate and NAD+, whereas its three products are acetoacetate, NADH, and H+. This enzyme belongs to the family of oxidoreductases, to be specific, those acting on the CH-OH group of donor with NAD+ or NADP+ as acceptor. This enzyme participates in synthesis and degradation of ketone bodies and butanoate metabolism. Applications: This enzyme is useful for enzymatic determination of ketone bodies (d-3-hydroxybutyrate and acetoacetate) in...ission Number: EC 1.1.1.30. CAS No. 9028-38-0. 3-HBDH. Mole weight: approx. 130 kDa (by gel filtration). Activity: Grade? 100U/mg-solid or more. Stability: Stable at-20°C for at least one year. Appearance: White amorphous powder, lyophilized. Source: Pseudomonas sp. (R)-3-hydroxybutanoate: NAD+ oxidoreductase; NAD+-beta-hydroxybutyrate dehydrogenase; hydroxybutyrate oxidoreductase; beta-hydroxybutyrate dehydrogenase; D-beta-hydroxybutyrate dehydrogenase; D-3-hydroxybutyrate dehydrogenase; D-(-)-3-hydroxybutyrate dehydrogenase; beta-hydroxybutyric acid dehydrogenase; 3-D-hydroxybutyrate dehydrogenase; beta-hydroxybutyric dehydrogenase; EC 1.1.1.30. Cat No: DIA-204.
In mammalian systems, β-hydroxybutyrate dehydrogenase is localized on the inner mitochondrial membrane and requires phosphatidyl choline for activity. In contrast, the enzyme from Pseudomonas is a soluble cytosolic enzyme that does not require a phospholipid allosteric activator. The enzyme is required for the utilization of ketone bodies as a source of metabolic energy. It catalyzes the oxidation of 3-hydroxybutyrate to acetoacetate, the first step in the conversion of ketone bodies to citric acid, which is then further metabolized via the tricarboxylic acid cycle (Krebs cycle). Applications: Suitable for the determination of acetoacetate and d (-)-3...nase; EC 1.1.1.30; 9028-38-0. Enzyme Commission Number: EC 1.1.1.30. CAS No. 9028-38-0. 3-HBDH. Activity: 250-750 units/mg protein. Storage: -20°C. Form: Lyophilized powder containing Tris buffer salts. Source: Rhodopseudomonas sphaeroides. 3-hydroxybutyrate dehydrogenase; 3-HBDH; NAD-β-hydroxybutyRate dehydrogenase; hydroxybutyRate oxidoreductase; β-hydroxybutyRate dehydrogenase; D-β-hydroxybutyRate dehydrogenase; D-3-hydroxybutyRate dehydrogenase; D-(-)-3-hydroxybutyRate dehydrogenase; β-hydroxybutyric acid dehydrogenase; 3-D-hydroxybutyRate dehydrogenase; β-hydroxybutyric dehydrogenase; EC 1.1.1.30; 9028-38-0. Cat No: NATE-0004.
poly(3-hydroxybutyrate) depolymerase
Reaction also occurs with esters of other short-chain-length (C1-C5) hydroxyalkanoic acids (HA). There are two types of polymers: native (intracellular) granules are amorphous and have an intact surface layer; denatured (extracellular) granules either have no surface layer or a damaged surface layer and are partially crystalline. Group: Enzymes. Synonyms: PHB depolymerase; poly(3HB) depolymerase; poly[(R)-hydroxyalkanoic acid] depolymerase; poly(HA) depolymerase; poly(HASCL) depolymerase; poly[(R)-3-hydroxybutyrate] hydrolase. Enzyme Commission Number: EC 3.1.1.75. CAS No. 9014-11-3. 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-3503; poly(3-hydroxybutyrate) depolymerase; EC 3.1.1.75; 9014-11-3; PHB depolymerase; poly(3HB) depolymerase; poly[(R)-hydroxyalkanoic acid] depolymerase; poly(HA) depolymerase; poly(HASCL) depolymerase; poly[(R)-3-hydroxybutyrate] hydrolase. Cat No: EXWM-3503.
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