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| Product | Description | |
|---|---|---|
| Butyric Acid FCC Natural | Butyric Acid FCC Natural. CAS No. 107-92-6. FEMA No. 2221. Kosher: Y. VIGON Item # 501217. Categories: Speciality Ingredients Suppliers, Flavors, Fragrances, Perfumers, Aromatherapy, Essential Oils. |  America & Internationally |
| Methyl-2 Butyric Acid Natural | Methyl-2 Butyric Acid Natural (Optically Active). CAS No. 116-53-0. FEMA No. 2695. Kosher: Y. VIGON Item # 501338. Categories: Speciality Ingrdients Suppliers, Flavors, Fragrances, Perfumers, Aromatherapy, Essetial Oils. | America & Internationally |
| Methyl-2 Butyric Acid Natural | Methyl-2 Butyric Acid Natural (Racemic). CAS No. 116-53-0. FEMA No. 2695. Kosher: Y. VIGON Item # 502130. Categories: Speciality Ingrdients Suppliers, Flavors, Fragrances, Perfumers, Aromatherapy, Essetial Oils. | America & Internationally |
| 2-Hydroxy-4-(methylthio)butyric acid | 2-Hydroxy-4-(methylthio)butyric acid is a dietary essential amino acid which is converted to Methionine (HY-13694) by 2-hydroxy acid dehydrogenase and 2-hydroxy acid oxidase. 2-Hydroxy-4-(methylthio)butyric acid is promising for research of gut disease [1]. Uses: Scientific research. Group: Natural products. CAS No. 583-91-5. Pack Sizes: 10 mM * 1 mL; 10 g; 25 g; 50 g. Product ID: HY-116688. |  |
| Hexanoic acid | Caproic acid is derived from the crude fermentation of butyric acid; or by fractional distillation of natural fatty acids. Used in various flavorings; manufacture of rubber chemicals; varnish dryers; resins; pharmaceuticals. Group: Fatty acids and ester homologs. Alternative Names: Caproic acid. CAS No. 142-62-1. Molecular formula: C6H12O2. Mole weight: 116.16g/mol. Appearance: Colorless liquid. Purity: 99%+. IUPACName: hexanoic acid. Canonical SMILES: CCCCCC(=O)O. Density: 0.92. ECNumber: 205-550-7;274-509-3. Catalog: ACM142621. |  |
| Hexanoic acid | Caproic acid is derived from the crude fermentation of butyric acid; or by fractional distillation of natural fatty acids. Used in various flavorings; manufacture of rubber chemicals; varnish dryers; resins; pharmaceuticals. Group: Solubility enhancing reagents. Alternative Names: Caproic acid. CAS No. 142-62-1. Pack Sizes: 25 kg/DRUMS. Product ID: hexanoic acid. Molecular formula: 116.16g/mol. Mole weight: C6H12O2. CCCCCC(=O)O. InChI=1S/C6H12O2/c1-2-3-4-5-6 (7)8/h2-5H2, 1H3, (H, 7, 8). FUZZWVXGSFPDMH-UHFFFAOYSA-N. 99%+. |  |
| Indole-3-butyric acid | Indole-3-butyric acid (3-indolebutyric acid) is a plant growth auxin and a good rooting agent. It can promote herbs and woody ornamental plant rooting and used for improving fruit rate. Indole 3-butyric acid is an auxin precursor, and is converted to indole 3-acetic acid (IAA) in a peroxisomal β-oxidation process [1]. Uses: Scientific research. Group: Natural products. Alternative Names: Indolebutyric acid. CAS No. 133-32-4. Pack Sizes: 10 mM * 1 mL; 5 g; 10 g. Product ID: HY-N0186. | |
| Indole-3-butyric acid (Standard) | Indole-3-butyric acid (Standard) is the analytical standard of Indole-3-butyric acid. This product is intended for research and analytical applications. Indole-3-butyric acid (3-indolebutyric acid) is a plant growth auxin and a good rooting agent. It can promote herbs and woody ornamental plant rooting and used for improving fruit rate. Indole 3-butyric acid is an auxin precursor, and is converted to indole 3-acetic acid (IAA) in a peroxisomal β-oxidation process [1]. Uses: Scientific research. Group: Natural products. CAS No. 133-32-4. Pack Sizes: 25 mg; 50 mg; 100 mg; 250 mg. Product ID: HY-N0186R. | |
| Monensin sodium salt | Sodium Monensin, isolated from Streptomyces cinnamonensis, is a well-known representative of naturally polyether ionophore antibiotics. It is widely used in ruminant animal feeds. Synonyms: Monensin A sodium salt; 2-[5-ethyltetrahydro-5-[tetrahydro-3-methyl-5-[tetrahydro-6-hydroxy-6-hydroxymethyl-3,5-dimethyl-2H-pyran-2-yl]-2-furyl]-2-furyl]-9-hydroxy-β-methoxy-α,γ,2,8-tetramethyl-1,6-dioxaspiro[4.5]decane-7-butyric acid, monosodium salt; A 3823A; Coban; Rumensin; NSC 343257. Grades: >98%. CAS No. 22373-78-0. Molecular formula: C36H61NaO11. Mole weight: 692.85. |  |
| 5-Hydroxy-2-adamantanone | 5-Hydroxy-2-adamantanone is used in the hydrosilylation of hydroxyketones. Also used in the preparation of adamantane substituted guanylhydrazones as inhibitors of butyrylcholinesterase, natural enzymes affecting succinic acid regulation. Group: Biochemicals. Alternative Names: 1-Hydroxy-4-adamantanone; 1-Hydroxy-4-ketoadamantane; 4-Oxo-1-adamantanol; 5-Hydroxy-2-adamantanone; 5-Hydroxyadamantanone; Idramantone; Kemantan; Kemantane; 5-Hydroxy-tricyclo[3.3.1.13, 7]decanone; 5-Hydroxytricyclo[3. 3. 1. 13, 7]decan-2-one. Grades: Highly Purified. CAS No. 20098-14-0. Pack Sizes: 2.5g. US Biological Life Sciences. |  Worldwide |
| Butyrospermum Parkii (Shea Butter) | Sheatree, Butyrospermum parkii, also known as Vitellaria paradoxa, is the source of Butyrospermum Parkii (Shea) Butter. When raw, it is ivory in colour and is frequently coloured yellow with palm oil or borutu root. It is used in numerous cosmetic and personal care products, such as bath and cleaning products, eye makeup, lotions and creams, suntan products, lipstick, and hair care products, where it functions as emollients and viscosity controllers. Uses: 1. moisturizer - shea butter is a natural emollient that helps to lock in moisture and improve skin hydration. it is easily absorbed into the skin and does not leave a residue. 2. anti-inflammatory - shea butter contains cinnamic acid, which has been shown to have anti-inflammatory properties. this makes it helpful in treating inflammatory skin conditions like acne, eczema, and psoriasis. 3. anti-. Group: Heterocyclic organic compound. Alternative Names: BUTYROSPERMUM PARKII (SHEA BUTTER);Fats and Glyceridic oils, shea butter;BUTYROSPERMUM PARKII (SHEA BUTTER LIQUID);SHEA BUTTER BUTYROSPERMUM PARKII. CAS No. 194043-92-0. Catalog: ACM194043920. | |
| Inulin | Inulin is an orally active prebiotic targeting the intestinal microbiota, selectively promoting the proliferation and activity of beneficial bacteria such as bifidobacteria and lactic acid bacteria, and playing a role in regulating the intestinal microecology. The functions of Inulin include: ? Fermentation by probiotics in the colon to produce short-chain fatty acids (such as butyrate and propionate), lowering the intestinal pH and inhibiting the overgrowth of harmful bacteria; ? Enhancing the intestinal barrier function and reducing endotoxin translocation; ? Directly scavenging free radicals (such as superoxide free radicals, hydroxyl free radicals) and activating antioxidant enzymes (SOD, CAT) to reduce oxidative stress. Inulin can also be used in the study of intestinal diseases (constipation, IBD), metabolic syndrome (diabetes, obesity) and liver damage by regulating glucose and lipid metabolism (such as reducing triglycerides, improving insulin sensitivity) and immune response (enhancing NK cell activity, inhibiting inflammatory factors) [1] [2] [3] [4]. Uses: Scientific research. Group: Natural products. CAS No. 9005-80-5. Pack Sizes: 100 mg. Product ID: HY-N7075. | |
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