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Yohimbine-[13C,d3] One of the isotopic labelled form of Yohimbine, an indole alkaloid compound, has been found to exhibit α2-adrenergic blocking effect and could be used in the treatment of neurological disorders. Synonyms: Yohimbine-(methyl-13C,d3 ester). Grade: ≥98% atom (CP); ≥99% atom. CAS No. 1261254-59-4. Molecular formula: C20[13C]H23D3N2O3. Mole weight: 358.45. BOC Sciences 2
Yohimbine Bark Extract (Ratio) Yohimbine Bark Extract (Ratio). Group: Others. Purity: 4:1~20:1. Yohimbine Bark Extract (Ratio). Cat No: EXTW-053. Creative Enzymes
Yohimbine Extract Strengthening muscular tension, increasing energy metabolism of human body. Uses: Designed for use in research and industrial production. Additional or Alternative Names: yohimbine extractive. Product Category: Material of medical care. Appearance: low purity: brownish red powder; white to off-white fine powde. CAS No. 65-19-0. Molecular formula: C21H26N2O3·HCL. Mole weight: 390.91. Product ID: ACM65190. Alfa Chemistry — ISO 9001:2015 Certified. Alfa Chemistry.
Yohimbine HCl Yohimbine HCl. Group: Biochemicals. Grades: Highly Purified. CAS No. 65-19-0. Pack Sizes: 2g, 5g, 10g, 25g, 50g. Molecular Formula: C21H26N2O3·HCl. US Biological Life Sciences. USBiological 8
Worldwide
Yohimbine HCL 8% & 98% HPLC Yohimbine HCL 8% & 98% HPLC. Pharma Resources International LLC
CA, FL & NJ
Yohimbine hydrochloride Yohimbine, an indole alkaloid derived from the bark of the Pausinystalia yohimbe tree in Central Africa, has been used as a mydriatic and in the treatment of impotence. It is also alleged to be an aphrodisiac. Uses: Antidepressant. Synonyms: CORYNINE HYDROCHLORIDE; APHRODINE HYDROCHLORIDE; APHROSOL HYDROCHLORIDE; 17-HYDROXYYOHIMBAN-16-CARBOXYLIC ACID METHYL ESTER HYDROCHLORIDE; 17A-HYDROXYYOHIMBAN-16A-CARBOXYLIC ACID METHYL ESTER HYDROCHLORIDE; YOHIMBE HCL; YOHIMBINE HCL; YOHIMBINE HYDROCHLORIDE. Grade: >98%. CAS No. 65-19-0. Molecular formula: C21H26N2O3·HCl. Mole weight: 390.9. BOC Sciences 9
Yohimbine Hydrochloride Indole alkaloid with α2-adrenergic blocking activity. Mydriatic. Used in the treatment of neurological disorders. Group: Biochemicals. Grades: Highly Purified. CAS No. 65-19-0. Pack Sizes: 1g. US Biological Life Sciences. USBiological 3
Worldwide
Yohimbine Hydrochloride United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standardspharma & vet compounds & metabolitespharma & vet compounds & metabolitesapi standardseuropean pharmacopoeia (ph. eur.)pharmaceutical toxicologypharmacopoeial standards. Alternative Names: NIH 9689, Yomax, Yohimbine chloride,Yohimbine hydrochloride, Benz[g]indolo[2,3-a]quinolizine, yohimban-16-carboxylic acid deriv., Dayto-Himbin, Aphrodyne, NSC 19509, Yohimbe, Yohimbex, Yohimban-16-carboxylic acid, 17-hydroxy-, methyl ester, monohydrochloride, (16alpha,17alpha)- (9CI), Yohimban-16alpha-carboxylic acid, 17alpha-hydroxy-, methyl ester, monohydrochloride (8CI), Thybine, Yohimbine monohydrochloride, Actibine, Erex, Yocon, Yohimex, Antagonil. Alfa Chemistry Analytical Products
Yohimbine Hydrochloride Yohimbine hydrochloride is an alpha-2 renal adenomatase receptor inhibitor, blocking pre- and post-contact alpha-2 renal adenomatase receptors, causing the release of renal adenoma and multiple sclerosis. Uses: Scientific research. Group: Natural products. CAS No. 65-19-0. Pack Sizes: 10 mM * 1 mL; 500 mg; 1 g. Product ID: HY-N0127. MedChemExpress MCE
Yohimbine Hydrochloride (17alpha-Hydroxyyohimban-16alpha-carboxylic Acid methyl Ester Hydrochloride, alpha2-Adrenoceptor Antagonist, Yohimbine Hydrochloride) A potent antagonist for alpha-2-adrenoceptors (pKi values are 8.52, 8.00 and 9.17 for human alpha-2a, alpha-2B and alpha-2C receptors respectively). Often used as pharmacological stressor in animal studies. Group: Biochemicals. Grades: Highly Purified. CAS No. 65-19-0. Pack Sizes: 1g. US Biological Life Sciences. USBiological 4
Worldwide
Yohimbine-(methyl-13C,d3 ester) ?99 atom %, ?98 atom % (CP). Group: Fluorescence/luminescence spectroscopy. Alfa Chemistry Analytical Products 2
Rauwolfia Vomitoria Root Bark P.E. Alpha Yohimbine HCL (Rauwolscine) 90% HPLC Rauwolfia Vomitoria Root Bark P.E. Alpha Yohimbine HCL (Rauwolscine) 90% HPLC. Pharma Resources International LLC
CA, FL & NJ
2,3-Dihydro-1,4-benzodioxin-2-carboximidic Acid Ethyl Ester Hydrochloride 2,3-Dihydro-1,4-benzodioxin-2-carboximidic Acid Ethyl Ester Hydrochloride is an intermediate in the synthesis of Idazoxan Hydrochloride (I506800), which is an α-adrenoceptor antagonist; in rat brain Idazoxan is a pure antagonist and it has a selectivity for α2- over α1-receptors markedly superior to Piperoxane, Yohimbine, or Rauwolscine. Antiparkinsonian. Group: Biochemicals. Grades: Highly Purified. CAS No. 79944-55-1. Pack Sizes: 100mg, 250mg. Molecular Formula: C11H13NO3; HCl, Molecular Weight: 207.233645999999. US Biological Life Sciences. USBiological 10
Worldwide
GPCR-Helix 8 Signaling Inhibitor, JF5 (GPCR-H8 Signaling Inhibitor, JF5, 4-Pentyl-2,3-dihydro-1H-cyclopenta[b]quinolin-9-imine, HI, 4-Pentyl-1,2,3,4-tetrahydro-9H-cyclopenta[b]quinolin-9-imine, HI) A cell-permeable quinolinimine compound that acts as a selective, potent blocker of G-protein coupled receptors (GPCR) that contain a constrained eighth helix (H8). The inhibition is selective and blocks G-protein signaling mediated via Gaq, but not Ga12. A non-orthosteric antagonist of PAR1 (IC50=4uM) that is shown to inhibit PAR1 and CCR-4 induced platelet aggregation without affecting PAR4 mediated aggregation. Shown to inhibit thrombus formation following vascular injury (IC50 ~1mg/kg). Also acts as a potent, non-competitive blocker of a2A-adrenergic receptors (IC50=2.5uM as shown by a decrease in 3H-yohimbine binding). Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 10mg. US Biological Life Sciences. USBiological 4
Worldwide
methyl (16alpha,17beta)-17-hydroxyyohimban-16-carboxylate β-Yohimbine isolated from the peel of Corynante yohimbe. Uses: Anti-plasmodial and anti-malarial activity. Synonyms: methyl (16alpha,17beta)-17-hydroxyyohimban-16-carboxylate; Amsonin. Grade: 0.98. CAS No. 549-84-8. Molecular formula: C21H26N2O3. Mole weight: 354.5. BOC Sciences 9
Rauwolscine Rauwolscine is a selective α2-adrenoceptor antagonist that inhibits tumor growth and induces apoptosis [1]. Uses: Scientific research. Group: Natural products. Alternative Names: α-Yohimbine; Corynanthidine; Isoyohimbine. CAS No. 131-03-3. Pack Sizes: 5 mg; 10 mg. Product ID: HY-12710. MedChemExpress MCE
Rauwolscine hydrochloride Rauwolscine hydrochloride is a potent and specific α2 adrenergic receptor antagonist with a K i of 12 nM. Uses: Scientific research. Group: Natural products. Alternative Names: α-Yohimbine hydrochloride; Corynanthidine hydrochloride; Isoyohimbine hydrochloride. CAS No. 6211-32-1. Pack Sizes: 1 mg. Product ID: HY-12710A. MedChemExpress MCE
Yohimbe bark Yohimbe bark. Group: Biochemicals. Alternative Names: Yohimbine. Grades: Highly Purified. CAS No. 146-48-5. Pack Sizes: 1g, 2g, 5g, 10g, 25g. US Biological Life Sciences. USBiological 8
Worldwide
Yohimbe Extract Yohimbe Extract. Applications: Used for men health care products, dietary supplements, treat sexual impotence and sexual dysfunction. Group: Others. Synonyms: Yohimbe Extract; 65-19-0; Corynante Yohimbe. CAS No. 65-19-0. Purity: 8% Yohimbine by HPLC. Appearance: Red brown fine powder. Storage: 2 years under well storage situation and stored away from direct sun light. Source: Bark. Species: Corynante Yohimbe. Yohimbe Extract; 65-19-0; Corynante Yohimbe; plant extract. Pack: 25KG/Drum with double plastic bag of foodstuff inside. Cat No: EXTW-077. Creative Enzymes
2-Propen-1,1,2,3,3-d5-1-ol 2-Propen-1,1,2,3,3-d5-1-ol is isotopically labelled form of Allyl Alcohol, which is used in the synthesis of yohimbinoid alkaloids venenatine and alstovenine. Also used in the synthesis of polycyclic alkaloid (-)-nakadomarin A. Group: Biochemicals. Grades: Highly Purified. CAS No. 102910-30-5. Pack Sizes: 5mg, 10mg. Molecular Formula: C3HD5O. US Biological Life Sciences. USBiological 10
Worldwide
Allyl Alcohol Allyl Alcohol is used in the synthesis of yohimbinoid alkaloids venenatine and alstovenine. Also used in the synthesis of (-)-nakadomarin A, a polycyclic alkaloid. Group: Biochemicals. Alternative Names: 2-Propen-1-ol;1-Hydroxy-2-propene; 1-Propen-3-ol; 2-Propenol; 2-Propenyl Alcohol; 3-Hydroxy-1-propene; 3-Hydroxypropene; Allylic Alcohol; NSC 6526; Shell Unkrauttod A; Vinylcarbinol. Grades: Highly Purified. CAS No. 107-18-6. Pack Sizes: 10g. US Biological Life Sciences. USBiological 3
Worldwide

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