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| Product | Description | |
|---|---|---|
| Sucrose acetate isobutyrate | Sucrose acetate isobutyrate. Synonyms: SUCROSE ACETATE ISOBUTYRATE;sucrose acetate isobutyrate(SAIB);99.5% SAIB Sucrose acetate isobutyrate;Sucrose acetate isobutyrate USP/BP/EP;TIANFU-CHEM Sucrose acetate isobutyrate. CAS No. 34482-63-8. Product ID: CDF4-0108. Molecular formula: C18H30O13. Category: Food Emulsifiers. Product Keywords: Food Ingredients; Food Emulsifiers; Sucrose acetate isobutyrate; CDF4-0108; 34482-63-8; C18H30O13; 204-771-6; 34482-63-8. Purity: 0.99. EC Number: 204-771-6. Boiling Point: 288 °C(lit.). Melting Point: 7 °C(lit.). Density: 1.146 g/mL at 25 °C(lit.). |  |
| Sucrose acetate isobutyrate | Use as emulsifying agent, dispersing agent. Use as plasticizer. Group: Non-ionic surfactants. Alternative Names: Sucrose di(acetate) hexaisobutyrate;SAIB;alpha-D-Glucopyranoside, 6-O-acetyl-1,3,4-tris-O-(2-methyl-1-oxopropyl)-beta-D-fructofuranosyl, 6-acetate 2,3,4-tris(2-methylpropanoate). CAS No. 126-13-6. Molecular formula: C40H62O19. Mole weight: 846.91. Appearance: Clear colorless to slightly yellow viscous liquid. Density: 1.22 g/cm³. Catalog: ACM126136. |  |
| Sucrose Acetate Isobutyrate | Sucrose Acetate Isobutyrate. Synonyms: SAIB. CAS No. 126-13-6. Pack Sizes: 100 g. Product ID: CDC10-0282. Molecular formula: C40H62O19. Category: Cosmetic Plasticizers. Product Keywords: Cosmetic Ingredients; Cosmetic Plasticizers; Sucrose Acetate Isobutyrate; CDC10-0282; 126-13-6; C40H62O19; SAIB; MFCD00041859; 126-13-6. Grade: Kosher. Purity: 0.99. Color: Clear colorless to slightly yellow. Physical State: Liquid. Quality Level: 400. Boiling Point: 288 °C. Melting Point: -83°C. Density: 1.146 g/mL at 25 °C. | |
| Sucrose 6'-Acetate, Technical grade 80% | Sucrose 6'-Acetate is a compound useful in organic synthesis. Synonyms: β-D-Fructofuranosyl α-D-Galactopyranoside 6-Acetate. Grades: 80%. CAS No. 936001-72-8. Molecular formula: C14H24O12. Mole weight: 384.33. |  |
| Sucrose octaacetate | Sucrose octaacetate is an acetylated derivative of sucrose with an intensely bitter tasting and can be used as bitter tasting surrogate. Sucrose octaacetate can be used as food additive and also used as an adhesive and plasticizer. Sucrose octaacetate also used in many pesticides, insecticides, and other toxic products as a deterrent to accidental poisoning. Sucrose octaacetate can also be used as an in situ seed and a soft template to synthesize polyaniline (PANI) nanofibers [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. CAS No. 126-14-7. Pack Sizes: 10 mM * 1 mL; 500 mg. Product ID: HY-119309. |  |
| Sucrose octaacetate | Sucrose octaacetate is used as an alcohol denaturant in pharmaceutical preparations. It is also used as a bittering agent and to prevent nail-biting or thumb-sucking. Synonyms: Acetic acid [(2S,3S,4R,5R)-4-acetoxy-2,5-bis(acetoxymethyl)-2-[[(2R,3R,4S,5R,6R)-3,4,5-triacetoxy-6-(acetoxymethyl)-2-tetrahydropyranyl]oxy]-3-tetrahydrofuranyl]ester; D-Saccharose octaacetate; Octa-O-acetyl D-(+)-Sucrose; 1,3,4,6-Tetra-O-acetyl-β-D-fructofuranosyl α-D-Glucopyranosid 2,3,4,6-Tetraacetate; 2,3,4,6,1',3',4',6'-Octa-O-acetylsucrose; NSC 1695; D-(+)-Saccharose Octaacetate; Octaacetyl Sucrose; Saccharose Octaacetate; α-D-Glucopyranoside, 1,3,4,6-tetra-O-acetyl-β-D-fructofuranosyl, 2,3,4,6-tetraacetate; α-D-Glucopyranoside, 1,3,4,6-tetra-O-acetyl-β-D-fructofuranosyl, tetraacetate; Monopet SOA; Octa-O-acetylsucrose. Grades: ≥98%. CAS No. 126-14-7. Molecular formula: C28H38O19. Mole weight: 678.59. | |
| 2,3,1,3,4,6-Hexa-O-acetyl-sucrose | Synonyms: Sucrose 1',2,3,3',4',6'-hexaacetate; 1',2,3,3',4',6'-Hexa-O-acetylsucrose; 1',2,3,3',4',6'-Hexa-O-acetyl-sucrose; 6-(Hydroxymethyl)tetrahydropyran-2-yl)oxy-tetrahydrofuran-2-yl)methyl acetate;(2S,3S,4R,5R)-2,5-Bis(acetoxymethyl)-2-(((2R,3R,4S,5R,6R)-3,4-diacetoxy-5-hydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)oxy)tetrahydrofuran-3,4-diyl diacetate.ALPHA.-D-GLUCOPYRANOSIDE, 1,3,4,6-TETRA-O-ACETYL-.BETA.-D-FRUCTOFURANOSYL, 2,3-DIACETATE ((2R,3R,4S,5S)-3,4-DIACETOXY-5-(ACETOXYMETHYL)-5-((2R,3R,4S,5R,6R)-3,4-DIACETOXY-5-HYDROXY-; alpha-D-Glucopyranoside, 1,3,4,6-tetra-O-acetyl-beta-D-fructofuranosyl, 2,3-diacetate ((2R,3R,4S,5S)-3,4-diacetoxy-5-(acetoxymethyl)-5-((2R,3R,4S,5R,6R)-3,4-diacetoxy-5-hydroxy-. CAS No. 52706-47-5. Molecular formula: C24H34O17. Mole weight: 594.5. | |
| 3,4,2,3,6-Penta-O-acetylsucrose | 3,4,2,3,6-Penta-O-acetylsucrose is a crucial component in the biomedical industry as it is used in the development of drugs aimed at treating various diseases. Additionally, it plays a vital role in drug delivery systems and formulation development, ensuring efficient and targeted drug release for enhanced therapeutic outcomes. Synonyms: Sucrose 2,3,3',4',6-pentaacetate; EINECS 252-768-3; 2,3,3',4',6-Penta-O-acetylsucrose; 2,3,6,3',4'-Penta-O-acetylsucrose; [(2R,3R,4S,5R,6R)-4,5-diacetyloxy-6-[(2S,3S,4R,5R)-3,4-diacetyloxy-2,5-bis(hydroxymethyl)oxolan-2-yl]oxy-3-hydroxyoxan-2-yl]methyl acetate; (2R,3R,4S,5R,6R)-6-(acetoxymethyl)-2-(((2S,3S,4R,5R)-3,4-diacetoxy-2,5-bis(hydroxymethyl)tetrahydrofuran-2-yl)oxy)-5-hydroxytetrahydro-2H-pyran-3,4-diyl diacetate; 2,3,6,3',4'-PENTAACETYLSUCROSE; 3,4-di-O-acetylhex-2-ulofuranosyl 2,3,6-tri-O-acetylhexopyranoside.ALPHA.-D-GLUCOPYRANOSIDE, 3,4-DI-O-ACETYL-.BETA.-D-FRUCTOFURANOSYL, 2,3,6-TRIACETATE. CAS No. 35867-25-5. Molecular formula: C22H32O16. Mole weight: 552.49. | |
| Acetylated Sucrose Distearate | Non-ionic Surfactants. Alternative Names: ACETYLATED SUCROSE DISTEARATE.alpha.-D-Glucopyranoside. beta.-D-fructofuranosyl, acetate dioctadecanoate. CAS No. 121684-92-2. Catalog: ACM121684922. | |
| Carbomer 980P | Carbomers are white-colored, fluffy, acidic, hygroscopic powders with a characteristic slight odor. A granular carbomer is also available (Carbopol 71G). CAS No. 139637-85-7. Product ID: PE-0566. Category: Thickeners; Binders; Emulsifiers; Suspending Agentss; Carrier Bases, etc. Product Keywords: Excipients for Liquid Dosage Form; Emulsifier Excipients; PE-0566; Carbomer 980P; Thickeners; Binders; Emulsifiers; Suspending Agentss; Carrier Bases, etc; ; 139637-85-7. UNII: NA. Chemical Name: Carbomer 980. Grade: Pharmceutical Excipients. Administration route: Oral; ophthalmic, rectal, topical, transdermal ; vaginal. Dosage Form: Oral suspensions, tablets; ophthalmic, rectal, topical, transdermal preparations; vaginal suppositories. Stability and Storage Conditions: Carbomers are stable, hygroscopic materials that may be heated at temperatures for up to 2 hours without affecting their thickening efficiency. However, exposure to excessive temperatures can result in discoloration and reduced stability. Source and Preparation: Carbomers are synthetic, high-molecular-weight, crosslinked polymers of acrylic acid. These acrylic acid polymers are crosslinked with allyl sucrose or allyl pentaerythritol. The polymerization solvent used previously was benzene; however, some of the newer commercially available grades of carbomer are manufactured using either ethyl acetate or a cyclohexane-ethyl acetate cosolvent mixture. The Carbo | |
| Native Baker's yeast (S. cerevisiae) S-Acetyl-coenzyme A synthetase | Acetyl-coenzyme A synthetase catalyzes the production of acetyl-CoA. It is involved in histone acetylation in the nucleus. It may be involved in the growth of nonfermentable carbon sources such as glycerol. Acetyl-coenzyme A synthetase is induced by acetate, acetaldehyde and ethanol. Applications: S-acetyl-coenzyme a synthetase may be used to study various metabolic pathways, such as glycolysis, gluconeogenesis, pyruvate metabolism and co fixation. it may also be used in gene expression studies. Group: Enzymes. Synonyms: acetyl-CoA synthetase; acetyl activating enzyme; acetate thiokinase; acyl-activating enzyme; acetyl coenzyme A synthetase; acetic thiokinase; acetyl CoA ligase; acetyl C. Enzyme Commission Number: EC 6.2.1.1. CAS No. 9012-31-1. ACS. Activity: > 3 units/mg protein. Storage: -20°C. Form: Lyophilized powder containing stabilizers as potassium phosphate, sucrose, and reduced glutathione. Source: Baker's yeast (S. cerevisiae). acetyl-CoA synthetase; acetyl activating enzyme; acetate thiokinase; acyl-activating enzyme; acetyl coenzyme A synthetase; acetic thiokinase; acetyl CoA ligase; acetyl CoA synthase; acetyl-coenzyme A synthase; short chain fatty acyl-CoA synthetase; short-chain acyl-coenzyme A synthetase; ACS; EC 6.2.1.1; 9012-31-1. Pack: Package size based on protein content. Cat No: NATE-0026. |  |
| Native Klebsiella pneumoniae Citrate Lyase | Citrate lyase is found in several microorganisms and catalyzes the first step of Citrate degradation, forming acetate and oxaloacetate. The enzyme contains 3 polypeptide subunits, α-subunit (a transferase), β-subunit (acyl lyase) and γ-subunit (acyl-carrier protein). Group: Enzymes. Synonyms: EC 4.1.3.6, citrase; citRatase; citritase; citridesmolase; Citrate aldolase; citric aldolase; Citrate lyase; Citrate oxaloacetate-lyase; Citrate oxaloacetate-lyase [(pro-3S)-CH2COO-?acetate]; 9012-83-3. Enzyme Commission Number: EC 4.1.3.6. CAS No. 9012-83-3. Citrase. Activity: > 0.20 unit/mg solid. Storage: 2-8°C. Form: Lyophilized powder containing bovine serum albumin, sucrose, MgSO4 and EDTA. Source: Klebsiella pneumoniae. EC 4.1.3.6, citrase; citRatase; citritase; citridesmolase; Citrate aldolase; citric aldolase; Citrate lyase; Citrate oxaloacetate-lyase; Citrate oxaloacetate-lyase [(pro-3S)-CH2COO-?acetate]; 9012-83-3. Cat No: NATE-0135. | |
| Native Pseudomonas lemoignei β-Hydroxybutyrate Dehydrogenase | 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. | |
| Sucrose-6-acetic ester | Sucrose-6-acetic ester, a revolutionary biomedical marvel, emerges as a crucial catalyst for combating an array of afflictions. With its unparalleled potential, this pharmaceutical intermediate orchestrates the synthesis of drugs specifically tailored to tackle inflammatory responses, cancerous growths, and neurodegenerative complexities. Synonyms: SUCROSE-6-ACETIC ESTER; Sucrose-6-aceticester; 63648-81-7; [(2R,3S,4S,5R,6R)-6-[(2S,3S,4S,5R)-3,4-dihydroxy-2,5-bis(hydroxymethyl)oxolan-2-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl acetate; Sucrose 6'-Acetate, Technical grade 80%; SCHEMBL891536; 936001-72-8. CAS No. 63648-81-7. Molecular formula: C14H24O12. Mole weight: 384.33. | |
| Sucrose acetoisobutyrate | Sucrose acetoisobutyrate is a prominent compound extensively employed in the biomedical sector assuming a critical role as an excipient within pharmaceutical formulations, especially those designated for oral administration. Notably, this compound exhibits exceptional attributes that bolster the stability and bioavailability of drugs. Synonyms: SAIB; Sucrose acetate isobutyrate; Sucrose diacetate hexaisobutyrate. CAS No. 126-13-6. Molecular formula: C40H62O19. Mole weight: 846.91. | |
| 2,3,1,3,4,6-Hexa-O-acetyl-6-O-methacryloyl-sucrose | | |
| 6-O-Benzoyl-2,3,6,3,4,-penta-O-acetyl-sucrose | | |
| Isomalt | Isomalt. Synonyms: Hydrogenated isomaltulose; hydrogenated palatinose. CAS No. 64519-82-0. Product ID: PE-0494. Category: Sweetening agent. Product Keywords: Pharmaceutical Excipients; Excipients for Solid Dosage Form; Isomalt; Sweeteners Excipients; Sweetening agent; 64519-82-0; 64519-82-0. UNII: S870P55O2W. Stability and Storage Conditions: Isomalt has very good thermal and chemical stability. When it is melted, no changes in the molecular structure are observed. It exhibits considerable resistance to acids and microbial influences.Isomalt is non-hygroscopic, and at 25°C does not significantly absorb additional water up to a relative humidity (RH) of 85%; paracetamol (acetaminophen) tablets based on isomalt were stored for 6 months at 85% RH at 208C and retained their physical aspect. If stored under normal ambient conditions, isomalt is chemically stable for many years. When it is stored in an unopened container at 20°C and 60% RH, a re-evaluation after 3 years is recommended. Isomalt does not undergo browning reactions; it has no reducing groups, and therefore it does not react with other ingredients in a formulation (e.g. with amines in Maillard reactions). Source and Preparation: Isomalt is produced from food-grade sucrose in a two-stage process.Beet sugar is converted by enzymatic transglucosidation into the reducing disaccharide isomaltulose. This undergoes catalytical hydrogenation to produce isomalt. Safety: Isomal | |
| N-Acylmannosamine 1-Dehydrogenase from Pseudomonas sp., Recombinant | In enzymology, a N-acylmannosamine 1-dehydrogenase (EC 1.1.1.233) is an enzyme that catalyzes the chemical reaction:N-acyl-D-mannosamine + NAD+<-> N-acyl-D-mannosaminolactone + NADH + H+. Thus, the two substrates of this enzyme are N-acyl-D-mannosamine and NAD+, whereas its 3 products are N-acyl-D-mannosaminolactone, NADH, and H+. This enzyme belongs to the family of oxidoreductases, specifically those acting on the CH-OH group of donor with NAD+ or NADP+ as acceptor. Group: Enzymes. Synonyms: N-acylmannosamine 1-dehydrogenase; EC 1.1.1.233; N-acylmannosamine dehydrogenase; N-acetyl-D-mannosamine dehydrogenase; N-acyl-D-mannosamine dehydrogenase; N-acylmannosamine dehydrogenase; 117698-08-5. Enzyme Commission Number: EC 1.1.1.233. CAS No. 117698-08-5. N-acylmannosamine 1-dehydrogenase. Mole weight: mol wt ~120 kDa (gel filtration). Activity: > 45 units/mg protein. Storage: -20°C. Form: lyophilized powder; Powder also contains bovine albumin and sucrose. Source: E. coli. Species: Pseudomonas sp. N-acylmannosamine 1-dehydrogenase; EC 1.1.1.233; N-acylmannosamine dehydrogenase; N-acetyl-D-mannosamine dehydrogenase; N-acyl-D-mannosamine dehydrogenase; N-acylmannosamine dehydrogenase; 117698-08-5. Cat No: NATE-0470. | |
| N,N'-diacetylchitobiose phosphorylase | The enzyme is specific for N,N'-diacetylchitobiose and does not phosphorylate other N-acetylchitooligosaccharides, cellobiose, trehalose, lactose, maltose or sucrose. Group: Enzymes. Synonyms: chbP (gene name). Enzyme Commission Number: EC 2.4.1.280. 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-2513; N,N'-diacetylchitobiose phosphorylase; EC 2.4.1.280; chbP (gene name). Cat No: EXWM-2513. | |
| Stevioside hydrate (BRN 0077427, CCRIS 6116) | Noncaloric natural sweetener, 300 times more potent than sucrose. Antidiabetic. Antihyperglycaemic and antihypoglycaemic. Potentiates insulin secretion. Enhances acetyl-CoA carboxylase (ACC) gene expression. Increases insulin sensitivity. Antihypertensive. Ca2+ influx inhibitor. Anticancer compound. Chemopreventive. Anti-inflammatory. IKKbeta, NF-kappaB and MAPK signaling inhibitor. Induces TNF-alpha, IL-1beta and nitric oxide release. Immunomodulator. Increasees phagocytic activity, haemagglutination antibody titre, delayed type hypersensitivity. Increased proliferation in LPS and Con A stimulated B and T cells. Peripheral me-opioid receptors activator. Important for regulation of glucose homeostasis. Anti-atherosclerotic. Group: Biochemicals. Alternative Names: BRN 0077427, CCRIS 6116. Grades: Highly Purified. CAS No. 57817-89-7 (anhy). Pack Sizes: 10mg, 50mg. Molecular Formula: C38H60O18. xH2O. US Biological Life Sciences. |  Worldwide |
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