Find where to buy products from suppliers in the USA, including: distributors, industrial manufacturers in America, bulk supplies and wholesalers of raw ingredients & finished goods.
Search for products or services, then visit the American suppliers website for prices, SDS or more information. You can also view suppliers in Australia, NZ or the UK.
| Product | Description | |
|---|---|---|
| SAG | A potent agonist of Hedgehog (Hh) signalling by activating the Smoothened (Smo) protein function. Studies identify novel properties of molecules displaying potential interest in the treatment of various cancers and brain diseases, and demonstrate that Smo is capable of signaling through G15. Group: Biochemicals. Grades: Highly Purified. CAS No. 912545-86-9. Pack Sizes: 1mg. Molecular Formula: C??H??ClN?OS. US Biological Life Sciences. |  Worldwide |
| SAG | SAG is a potent Smoothened (Smo) receptor agonist ( EC 50 =3 nM; K d =59 nM). SAG activates the Hedgehog signaling pathway and counteracts Cyclopamine (HY-17024) inhibition of Smo [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. CAS No. 912545-86-9. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-12848. |  |
| SAG | SAG is a potent Smoothened (Smo) receptor agonist (Kd = 59 nM); sag antagonizes cyclopamine action at the Smo receptor. Synonyms: SAG. Grades: 98%. CAS No. 912545-86-9. Molecular formula: C28H28ClN3OS. Mole weight: 490.06. |  |
| SAG 21k | SAG 21k is a potent, brain penetrating and orally available activator of Hedgehog signaling (EC50 = 0.4 nM). Synonyms: 3-Chloro-4, 7-difluoro-N-[[2-methoxy-5- (4-pyridinyl) phenyl]methyl]-N-trans-4- (methylamino) cyclohexyl]benzo[b]thiophene-2-carboxamide. Grades: ≥98% by HPLC. CAS No. 946002-48-8. Molecular formula: C29H28ClF2N3O2S. Mole weight: 556.07. | |
| SAG Analog | Cell permeable low toxicity Sonic hedgehog (Shh) agonist. Cell permeable smoothened (Smo) agonist. Potent activator of VEGF expression in vitro. Group: Biochemicals. Grades: Highly Purified. CAS No. 1401532-78-2. Pack Sizes: 1mg. Molecular Formula: C28H27Cl2N3OS (trans-isomer). US Biological Life Sciences. | Worldwide |
| SAG Analog (cis-isomer) (Compound 10b, 3, 4-Dichloro-N- (cis-4- (methylamino) cyclohexyl) -N- (3-pyridin-4-ylbenzyl) benzo[b]thiophene-2-carboxamide) | A cell-permeable, highly active, Sonic hedgehog (Shh) signaling agonist. Smoothened (Smo) agonist. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 500ug, 1mg. US Biological Life Sciences. | Worldwide |
| SAG Analog (highly active) (Compound 10b, 3, 4-Dichloro-N- (cis-4- (methylamino) cyclohexyl) -N- (3-pyridin-4-ylbenzyl) benzo[b]thiophene-2-carboxamide) | Cell permeable highly active Sonic hedgehog (Shh) agonist. Group: Biochemicals. Alternative Names: Compound 10b, 3, 4-Dichloro-N- (cis-4- (methylamino) cyclohexyl) -N- (3-pyridin-4-ylbenzyl) benzo[b]thiophene-2-carboxamide. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| SAG Analog (trans-isomer) (Compound 10c, 3, 4-Dichloro-N- (trans-4- (methylamino) cyclohexyl) -N- (3-pyridin-4-ylbenzyl) benzo[b]thiophene-2-carboxamide) | A cell-permeable, low toxicity, Sonic hedgehog (Shh) signaling agonist. Smoothened (Smo) agonist. Also acts as a potent activator of VEGF expression in vitro. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 500ug , 1mg. US Biological Life Sciences. | Worldwide |
| SAG dihydrochloride | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopy. |  |
| SAG dihydrochloride | SAG dihydrochloride is a potent Smoothened (Smo) receptor agonist ( EC 50 =3 nM; K d =59 nM). SAG dihydrochloride activates the Hedgehog signaling pathway and counteracts Cyclopamine (HY-17024) inhibition of Smo [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. CAS No. 2702366-44-5. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 50 mg. Product ID: HY-12848C. | |
| SAG dihydrochloride | SAG is a potent and cell-permeable Smoothened (Smo) receptor agonist that regulates hedgehog signaling. SAG inhibits hedgehog signaling at high concentrations. Synonyms: 3-Chloro-N-[trans-4- (methylamino) cyclohexyl]-N-[[3- (4-pyridinyl) phenyl]methyl]benzo[b]thiophene-2-carboxamide dihydrochloride. Grades: ≥99% by HPLC. Molecular formula: C28H28ClN3OS.2HCl. Mole weight: 562.98. | |
| SAG Dihydrochloride (Water Soluble) (N-Methyl-N?- (3-pyridinylbenzyl) -N?- (3-chlorobenzo [b]thiophene-2-carbonyl) -1, 4-diaminocyclohexane. 2HCl) | Cell permeable Sonic hedgehog (Shh) agonist. Cell permeable smoothened (Smo) agonist. Induces Sonic hedgehog (Shh) pathway activation and counteracts cyclopamine inhibition of Smo. Acts as an activator of Smo at low concentrations and as an inhibitor of Smo at very high concentrations. Potent activator of VEGF expression in vitro. Group: Biochemicals. Grades: Highly Purified. CAS No. 364590-63-6. Pack Sizes: 1mg, 5mg. US Biological Life Sciences. | Worldwide |
| SAG dihydrocloride | SAG dihydrocloride. Group: Biochemicals. Grades: Highly Purified. CAS No. 364590-63-6. Pack Sizes: 5mg, 10mg, 25mg, 50mg, 100mg. US Biological Life Sciences. | Worldwide |
| Sage Extract | Sage Extract. Applications: Used for women skin health care products, beauty products. Group: Others. Synonyms: Sage Extract; Salvia officinalis Linn. Purity: 10:1 By TLC. Appearance: Brown yellow fine powder. Storage: 2 years under well storage situation and stored away from direct sun light. Source: Whole herb. Species: Salvia officinalis Linn. Sage Extract; Salvia officinalis Linn; plant extract. Pack: 20KG-25KG/Drum with double plastic bag of foodstuff inside. Cat No: EXTW-090. |  |
| Sage Ground Powder | Sage Ground Powder. |  CA, FL & NJ |
| Sage Leaf Powder | Sage Leaf Powder. | CA, FL & NJ |
| Sage oil, Spanish | Sage oil, Spanish. Uses: Designed for use in research and industrial production. Additional or Alternative Names: FEMA 3003;SAGE OIL, SPANISH TYPE;SAGE OIL DALMATIAN TYPE;SAGE OIL SPANISH RECON;SAGE OIL, SPANISH;SAGE OIL, DALMATION, SPANISH TYPE;SAGE OIL DALMATION;sagedalmatianoil. Product Category: Heterocyclic Organic Compound. CAS No. 8016-64-6. Molecular formula: CAS: 8016-64-6. Purity: Dalmatian type. Density: 0.912 g/mL at 25 °C(lit.). Product ID: ACM8016646. Alfa Chemistry ISO 9001:2015 Certified. |  |
| SAG hydrochloride | SAG hydrochloride is a potent Smoothened (Smo) receptor agonist ( EC 50 =3 nM; K d =59 nM). SAG hydrochloride activates the Hedgehog signaling pathway and counteracts Cyclopamine (HY-17024) inhibition of Smo [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. CAS No. 2095432-58-7. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-12848B. | |
| Sagittatoside A | Sagittatoside A is a natural compound isolated from traditional Chinese herb Yinyanghuo. Synonyms: Sagittatoside A; 118525-35-2; Icariin-A; 3-[(2S,3R,4R,5R,6S)-4,5-dihydroxy-6-methyl-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5,7-dihydroxy-2-(4-methoxyphenyl)-8-(3-methylbut-2-enyl)chromen-4-one; SCHEMBL4982932; CHEBI:197154; HY-N0873; CS-3690; MS-31069. Grades: >98%. CAS No. 118525-35-2. Molecular formula: C33H40O15. Mole weight: 676.24. | |
| Sagopilone | Sagopilone is a fully synthetic low-molecular-weight epothilone with potential antineoplastic activity. Sagopilone binds to tubulin and induces microtubule polymerization while stabilizing microtubules against depolymerization, which may result in the inhibition of cell division, the induction of G2/M arrest, and apoptosis. The agent is not a substrate for the P-glycoprotein (P-gp) efflux pump and so may exhibit activity in multidrug-resistant (MDR) tumors. The epothilone class of metabolites was originally isolated from the myxobacterium Solangium cellulosum. Synonyms: DE 03757; DE-03757; DE03757; ZK 219477; ZK219477; ZK-219477; ZK-EPO; (1S,3S,7S,10R,11S,12S,16R)-10-allyl-7,11-dihydroxy-8,8,12,16-tetramethyl-3-(2-methylbenzo[d]thiazol-5-yl)-4,17-dioxabicyclo[14.1.0]heptadecane-5,9-dione. CAS No. 305841-29-6. Molecular formula: C30H41NO6S. Mole weight: 543.72. | |
| SAG (Standard) | SAG (Standard) is the analytical standard of SAG. SAG is a potent Smoothened (Smo) receptor agonist ( EC 50 =3 nM; K d =59 nM). SAG activates the Hedgehog signaling pathway and counteracts Cyclopamine (HY-17024) inhibition of Smo [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. CAS No. 912545-86-9. Pack Sizes: 1 mg; 5 mg. Product ID: HY-12848R. | |
| 1-Deamino-1-hydroxysagamicin | 1-Deamino-1-hydroxysagamicin is an aminoglycoside antibiotic produced by micromonospora sagarmiensis SU-2 (KY11509). It has anti-gram-positive and negative bacteria activity. Synonyms: SU-3. CAS No. 72614-86-9. Molecular formula: C20H40N4O8. Mole weight: 464.55. | |
| CASCARA SAGRADA | Synonyms: Cascarillaabsolutecolourlessmd; Cascarillaoleoresin; Oils,cascarilla; CASCARA SAGRADA EXTRACT; CASCARA SAGRADA AROMATIC FLUID EXTRACT; CASCARA EXTRACT; CASCARA SAGRADA; CASCARA SAGRADA, FLUID EXTRACT. Grades: 95%. CAS No. 8007-6-5. | |
| Cascara Sagrada Powder | Cascara Sagrada Powder. | CA, FL & NJ |
| InSolution Smoothened Agonist, SAG | Smoothened Agonist, SAG, is a 10 mM (500 μg/86 μl) solution of Smoothened Agonist, SAG (Cat. No. 566660) in H?O. Group: Fluorescence/luminescence spectroscopy. | |
| Smoothened Agonist, SAG - CAS 364590-63-6 | A cell-permeable Smoothened Agonist, SAG, CAS 364590-63-6, modulates the coupling of Smo with its downstream effector by interacting with the Smo heptahelical domain (KD = 59 nM). Group: Fluorescence/luminescence spectroscopy. | |
| Smoothened Agonist, SAG (N-Methyl-N- (3-pyridinylbenzyl) -N- (3-chlorobenzo [b]thiophene-2-carbonyl) -1, 4-diaminocyclohexane, SAG1.3 ) | A cell-permeable benzothiophene compound that modulates the coupling of Smo with its downstream effector by interacting with the Smo heptahelical domain (=59nM). Shown to induce Smo internalization. Shown to induce Hedgehog pathway activation (EC50= ?3nM in NIH 3T3-derived Shh-LIGHT2 cells) and counteracts Cyclopamine-KAAD inhibition of Smo. Reported to act as an activator at low concentrations and as an inhibitor at very high concentrations. Group: Biochemicals. Grades: Highly Purified. CAS No. 364590-63-6. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| 1,8-cineole synthase | Requires Mn2+ or Zn2+. Mg2+ is less effective than either. 1,8-Cineole is the main product from the enzyme with just traces of other monoterpenoids. The oxygen atom is derived from water. The reaction proceeds via linalyl diphosphate and α-terpineol, the stereochemistry of both depends on the organism. However neither intermediate can substitute for geranyl diphosphate. The reaction in Salvia officinalis (sage) proceeds via (-)-(3R)-linalyl diphosphate while that in Arabidopsis (rock cress) proceeds via (+)-(3S)-linalyl diphosphate. Group: Enzymes. Synonyms: 1,8-cineole cyclase; geranyl pyrophoshate:1,8-cineole cyclase; 1,8-cineole synthetase. Enzyme Commission Number: EC 4.2.3.108. CAS No. 110637-19-9. 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-5119; 1,8-cineole synthase; EC 4.2.3.108; 110637-19-9; 1,8-cineole cyclase; geranyl pyrophoshate:1,8-cineole cyclase; 1,8-cineole synthetase. Cat No: EXWM-5119. | |
| 3''-N-demethyl gentamicin C1a | 3''-N-demethyl gentamicin C1a is an aminoglycoside antibiotic produced by Micromonospora sagamiensis G-665. CAS No. 59864-29-8. Molecular formula: C18H37N5O7. Mole weight: 435.52. | |
| (-)-α-pinene synthase | Cyclase II of Salvia officinalis (sage) gives about equal parts (-)-α-pinene, (-)-β-pinene and (-)-camphene, plus traces of other monoterpenoids. (3S)-Linalyl diphosphate can also be used by the enzyme in preference to (3R)-linalyl diphosphate. The 4-pro-S-hydrogen of geranyl diphosphate is lost. Requires Mg2+ (preferred to Mn2+). The enzyme from Abies grandis (grand fir) gives roughly equal parts (-)-α-pinene and (-)-β-pinene. However the clone ag11 gave 35% (-)-limonene, 24% (-)-α-pinene and 20% (-)-β-phellandrene. It requires Mn2+ and K+ (Mg2+ is ineffective). Synthase I from Pinus taeda (loblolly pine) produces (-)-α-pinene with traces...ve roughly equal proportions of (-)-α-pinene and (-)-camphene plus traces of other monoterpenoids. See also EC 4.2.3.120, (-)-β-pinene synthase; EC 4.2.3.117, (-)-camphene synthase; EC 4.2.3.16, (-)-limonene synthase; and EC 4.2.3.52, (-)-β-phellandrene synthase. Group: Enzymes. Synonyms: (-)-α-pinene/(-)-camphene synthase; (-)-α-pinene cyclase. Enzyme Commission Number: EC 4.2.3.119. 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-5131; (-)-α-pinene synthase; EC 4.2.3.119; (-)-α-pinene/(-)-camphene synthase; (-)-α-pinene cyclase. Cat No: EXWM-5131. | |
| (+)-α-pinene synthase | Cyclase I of Salvia officinalis (sage) gives about equal parts (+)-α-pinene and (+)-camphene, whereas cyclase III gives about equal parts of (+)-α-pinene and (+)-β-pinene. (3R)-Linalyl diphosphate can also be used by the enzyme in preference to (3S)-linalyl diphosphate. The 4-pro-R-hydrogen of geranyl diphosphate is lost. Requires Mg2+ (preferred to Mn2+). With synthase II of Pinus taeda (loblolly pine) (+)-α-pinene was the only product. Requires Mn2+ (preferred to Mg2+). See also EC 4.2.3.122, (+)-β-pinene synthase, and EC 4.2.3.116, (+)-camphene synthase. Group: Enzymes. Synonyms: (+)-α-pinene cyclase; cyclase I. Enzyme Commission Number: EC 4.2.3.121. 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-5134; (+)-α-pinene synthase; EC 4.2.3.121; (+)-α-pinene cyclase; cyclase I. Cat No: EXWM-5134. | |
| Antibiotic 477-2h | It is an aminoglycoside antibiotic produced by the strain of Micromonospora sagamiensis G-477. It has weak activity against gram-positive and gram-negative bacteria. Synonyms: 477-2H. CAS No. 72751-74-7. Molecular formula: C24H46N4O15. Mole weight: 630.64. | |
| Anticancerous peptide 1 | Anticancerous peptide 1 is an antimicrobial peptide produced by Cycas revoluta (Sago palm). It has antibacterial and anticancer activity. Synonyms: Cr-ACP1; Ala-Trp-Lys-Leu-Phe-Asp-Asp-Gly-Val; Cycas revoluta-anticancerous peptide 1. Grades: ≥97%. Molecular formula: C50H71N11O14. Mole weight: 1050.18. | |
| (-)-β-pinene synthase | Cyclase II of Salvia officinalis (sage) produces about equal parts (-)-α-pinene, (-)-β-pinene and (-)-camphene, plus traces of other monoterpenoids. The enzyme, which requires Mg2+ (preferred to Mn2+), can also use (3S)-Linalyl diphosphate (preferred to (3R)-linalyl diphosphate). The enzyme from Abies grandis (grand fir) produces roughly equal parts of (-)-α-pinene and (-)-β-pinene. Cyclase IV from Pinus contorta (lodgepole pine) produces 63% (-)-β-pinene, 26% 3-carene, and traces of α-pinene. Synthase III from Pinus taeda (loblolly pine) forms (-)-β-pinene with traces of α-pinene and requires Mn2+ and K+ (Mg2+ is ineffective). A clone...a spruce) forms 30% (-)-β-pinene and 70% (-)-α-pinene. See also EC 4.2.3.119, (-)-α-pinene synthase, EC 4.2.3.117, (-)-camphene synthase, and EC 4.2.3.107 (+)-3-carene synthase. Group: Enzymes. Synonyms: β-geraniolene synthase; (-)-(1S,5S)-pinene synthase; geranyldiphosphate diphosphate lyase (pinene forming). Enzyme Commission Number: EC 4.2.3.120. 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-5133; (-)-β-pinene synthase; EC 4.2.3.120; β-geraniolene synthase; (-)-(1S,5S)-pinene synthase; geranyldiphosphate diphosphate lyase (pinene forming). Cat No: EXWM-5133. | |
| (+)-β-pinene synthase | Cyclase III from Salvia officinalis (sage) gives roughly equal parts of (+)-β-pinene and (+)-α-pinene. See EC 4.2.3.121, (+)-α-pinene synthase. Group: Enzymes. Synonyms: (+)-pinene cyclase; cyclase III. Enzyme Commission Number: EC 4.2.3.122. 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-5135; (+)-β-pinene synthase; EC 4.2.3.122; (+)-pinene cyclase; cyclase III. Cat No: EXWM-5135. | |
| (+)-bornyl diphosphate synthase | Requires Mg2+. The enzyme from Salvia officinalis (sage) can also use (3R)-linalyl diphosphate or more slowly neryl diphosphate in vitro. The reaction proceeds via isomeration of geranyl diphosphate to (3R)-linalyl diphosphate. The oxygen and phosphorus originally linked to C-1 of geranyl diphosphate end up linked to C-2 of (+)-bornyl diphosphate. cf. EC 5.5.1.22 [(-)-bornyl diphosphate synthase]. Group: Enzymes. Synonyms: bornyl pyrophosphate synthase (ambiguous); bornyl pyrophosphate synthetase (ambiguous); (+)-bornylpyrophosphate cyclase; geranyl-diphosphate cyclase (ambiguous); (+)-bornyl-diphosphate lyase (decyclizing). Enzyme Commission Number: EC 5.5.1.8. CAS No. 72668-91-8. 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-5634; (+)-bornyl diphosphate synthase; EC 5.5.1.8; 72668-91-8; bornyl pyrophosphate synthase (ambiguous); bornyl pyrophosphate synthetase (ambiguous); (+)-bornylpyrophosphate cyclase; geranyl-diphosphate cyclase (ambiguous); (+)-bornyl-diphosphate lyase (decyclizing). Cat No: EXWM-5634. | |
| (+)-camphene synthase | Cyclase I of Salvia officinalis (sage) gives about equal parts (+)-camphene and (+)-α-pinene. (3R)-Linalyl diphosphate can also be used by the enzyme in preference to (3S)-linalyl diphosphate. Requires Mg2+ (preferred to Mn2+). See also EC 4.2.3.121 (+)-α-pinene synthase. Group: Enzymes. Enzyme Commission Number: EC 4.2.3.116. 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-5128; (+)-camphene synthase; EC 4.2.3.116. Cat No: EXWM-5128. | |
| (+)-camphor 6-exo-hydroxylase | A cytochrome P-450 monooxygenase isolated from Salvia officinalis (sage). Involved in the catabolism of camphor in senescent tissue. Group: Enzymes. Synonyms: (+)-camphor 6-hydroxylase. Enzyme Commission Number: EC 1.14.13.161. 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-0761; (+)-camphor 6-exo-hydroxylase; EC 1.14.13.161; (+)-camphor 6-hydroxylase. Cat No: EXWM-0761. | |
| Casanthranol | Casanthranol is a concentrated mixture of anthranol glycosides from cascara sagrada (dried bark of Rhamnus p. ) and used as a laxative in constipation and various medical conditions, stimulant laxative Casanthranol encourages bowel movements by acting on the intestinal wall to increase muscle contractions [1]. Uses: Scientific research. Group: Natural products. CAS No. 8024-48-4. Pack Sizes: 500 mg; 1 g; 5 g. Product ID: HY-B2134. | |
| GANT58 (2,3,4,5-Tetra(4-pyridyl)thiophene; NSC75503) | Cell-permeable. Acts as a blocker of Hedgehog (Hh) pathway downstream of SMO and SUFU causing Gli1 nuclear accumulation. It also targets Gli-mediated gene transactivation (IC50 ~ 5uM in SAG-stimulated Shh-L2 cells) and displays anti-proliferative and antitumor activity in vivo. Group: Biochemicals. Alternative Names: 2,3,4,5-Tetra(4-pyridyl)thiophene; NSC75503. Grades: Highly Purified. CAS No. 64048-12-0. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| Gentamicin C2b | Micronomicin is a trisaccharide pentaaminoglycoside antibiotic belonging to the gentamicin class. It is isolated from micromonospora sagamiensis var. It has broad activity against Gram-positive and Gram-negative bacteria and induces neuromuscular obstruction. Synonyms: Micronomicin; Sagamicin; Santemycin; Antibiotic KW 1062; Antibiotic XK 62-2. Grades: >95% by HPLC. CAS No. 52093-21-7. Molecular formula: C20H41N5O7. Mole weight: 463.57. | |
| Herbicidin A | It is produced by the strain of Streptomyces saganoensis. It is a potent herbicide with selective activity against dicotyledonous plant and has anti-gram-positive bacterial activity. Synonyms: alpha-L-ido-D-lyxo-5-Undeculo-5,9-pyranosonic acid, 11-C-(6-amino-9H-purin-9-yl)-2,6:8,11-dianhydro-7-deoxy-10-O-methyl-, methyl ester, 4-(2-(hydroxymethyl)-2-butenoate), (4(E),11R)-; (11R)-11-C-(6-Amino-9H-purin-9-yl)-2,6:8,11-dianhydro-10-O-methyl-4-O-[(E)-1-oxo-2-(hydroxymethyl)-2-butenyl]-7-deoxy-α-L-ido-D-lyxo-5-undecoulo-5,9-pyranosonic acid methyl ester. Grades: >95% by HPLC. CAS No. 55353-31-6. Molecular formula: C23H29N5O11. Mole weight: 551.50. | |
| Herbicidin B | It is produced by the strain of Streptomyces saganoensis. It has herbicidal and anti-gram-positive bacterial activity. Synonyms: Herbicidine B; 9-(6,10-Anhydro-5-deoxy-11-methyl-2-O-methylundec-7-ulopyranosefuranosyluronosyl)-9H-purin-6-amine; (11R)-11-C-(6-Amino-9H-purin-9-yl)-2,6:8,11-dianhydro-10-O-methyl-7-deoxy-α-L-ido-D-lyxo-5-undecoulo-5,9-pyranosonic acid methyl ester. Grades: >95%. CAS No. 55353-32-7. Molecular formula: C18H23N5O9. Mole weight: 453.40. | |
| Hh Signaling Antagonist XII, MRT-83 (N- (2-Methyl-5- (3- (3, 4, 5-trimethoxybenzoyl) guanidino) phenyl) - (1, 1-biphenyl) -4-carboxamide) | A cell-permeable acylguanidine compound that is shown to block Hh signaling and act as a potent, reversible and high-affinity Smo (Smoothened) antagonist. Displays 20-60 -fold greater potency than Cyclopamine and competitively inhibits bodipy-cyclopamine binding to Smo (IC50 = 4.6 and 14nM in HEK293-hSMO and HEK293-mSMO cells, respectively). Represses ShhN (N-myristoylated Shh) signaling (IC50=15nM for Gli-dependent luciferase activity in Shh-light2 cells) and SAG- induced C3H10T1/2 cell differentiation (IC50=10nM in an alkaline phosphatase activity assay). Inhibits ShhN (3nM) and SAG (10nM)-mediated proliferation of rat cerebellar granule cell precursors (IC50 ~3 and 6nM, respectively). Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| HPI 1 | HPI 1 is a hedgehog (Hh) signaling inhibitor that blocks Sonic hedgehog (Shh)-, SAG- and Gli-induced Hh pathway activation in Shh-LIGHT2 cells (IC50 = 1.5, 1.5, 4 and 6 μM for Shh-, SAG-, Gli2- and Gli1-induced activation) with no effect on Wnt signaling. HPI 1 also inhibits Hh pathway activation in SmoM2-LIGHT cells (IC50 = 2.5 μM), and prevents the proliferation of cerebellar granule neuron precursors expressing SmoM2. Synonyms: HPI 1; HPI1; HPI-1; 1,4,5,6,7,8-Hexahydro-4-(3-hydroxyphenyl)-7-(2-methoxyphenyl)-2-methyl-5-oxo-3-quinolinecarboxylic acid 2-methoxyethyl ester. Grades: ≥95% by HPLC. CAS No. 599150-20-6. Molecular formula: C27H29NO6. Mole weight: 463.52. | |
| HPI 1 (1,4,5,6,7,8-Hexahydro-4-(3-hydroxyphenyl)-7-(2-methoxyphenyl)-2-methyl-5-oxo-3-quinolinecarboxylic acid 2-methoxyethyl ester) | Hedgehog (Hh) signaling inhibitor. Inhibits Sonic hedgehog (Shh)-, SAG- and Gli-induced Hh pathway activation in Shh-LIGHT2 cells (IC50 values are 1.5, 1.5, 4 and 6um for Shh-, SAG-, Gli2- and Gli1-induced activation). Also inhibits Hh pathway activation in SmoM2-LIGHT cells (IC50 = 2.5um); inhibits the proliferation of cerebellar granule neuron precursors expressing SmoM2. Does not inhibit Wnt signaling. Group: Biochemicals. Grades: Highly Purified. CAS No. 599150-20-6. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| Indazole-5-boronic acid pinacol ester | Indazole-5-boronic acid pinacol ester. Group: Salt. Alternative Names: BE09, MolPort-002-344-305, Indazole-5-boronic acid pinacol ester, OR30735, 862723-42-0. CAS No. 862723-42-0. Product ID: 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indazole. Molecular formula: 244.1. Mole weight: C13< / sub>H17< / sub>BN2< / sub>O2< / sub>. B1 (OC (C (O1) (C)C) (C)C)C2=CC3=C (C=C2)NN=C3. SAGPUUKLGWNGOS-UHFFFAOYSA-N. 95%. |  |
| Kaempferia Galanga (Galanga Root Oil) - CO2 | Galangal CO2 select is extracted from the dried rhizomes (underground stems) of Kaempferia galanga, a small tropical plant that is closely related to ginger; it is commonly cultivated in India, Indonesia, and Malaysia for essential oilsproduction, medicinal use, and as an ingredient in curry. Galangal Root oil is fresh, spicy, woody, ginger-like oil, steam distilled from the plant's rhizome. In fact, Galangal Root is closely related to true ginger and cardamom so it's not surprising that Galangal Root blends well with these oils and shares similar notes. Blends Well With: Black Pepper, Cardamom, Carnation, Cedarwood, Chamomile (Roman), Cinnamon, Clove, Coriander, Cypress, Elemi, Fennel, Frankincense, Geranium, Ginger, Jasmine, Juniper Berry, Laurel Leaf, Lavandin, Lavender, Liquidambar (Styrax), Marjoram, Myrrh, Myrtle, Orris, Palmarosa, Patchouli, Pine, Rose, Sage, Sandalwood, Spikenard, Tarragon, Vetiver. Uses: Pharmaceutical. Group: Plant Extracts. INCI Names: Kaempferia Galanga Root Oil. Grades: INDUSTRIAL GRADE. CAS No. 92347-13-2. Pack Sizes: 25 kgs Jerrycan, 200 kg Drums. Product ID: GL-001. Olfactive Profile: Fresh, spicy, characteristic odour of galanga. EC No: 296-200-2. Origin: Indonesia. |  New Jersey |
| Kunitz-type serine protease inhibitor 1 | Kunitz-type serine protease inhibitor 1 is a Kunitz protease inhibitor isolated from Xanthosoma sagittifolium. It has activity against gram-negative bacteria. Synonyms: Pro-Val-Val-Asp-Thr-Thr-Gly-Asn-Asn-Pro-Leu-Gln-Gln-Gln-Glu-Glu-Tyr-Tyr-Val. Grades: 96.4%. Molecular formula: C96H144N24O35. Mole weight: 2194.34. | |
| lavandulyl diphosphate synthase | Lavandulyl diphosphate is a monoterpene with a non-head-to-tail linkage. It is unlike most monoterpenoids, which are derived from geranyl diphosphate and have isoprene units that are linked head-to-tail. When this enzyme is incubated with dimethylallyl diphosphate and isopentenyl diphosphate, it also forms the regular monoterpene geranyl diphosphate. The enzyme from Artemisia tridentata (big sagebrush) forms both lavandulyl diphosphate and chrysanthemyl diphosphate (see EC 2.5.1.67, chrysanthemyl diphosphate synthase) when dimethylally diphosphate is the sole substrate. Group: Enzymes. Synonyms: FDS-5. Enzyme Commission Number: EC 2.5.1.69. 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-2806; lavandulyl diphosphate synthase; EC 2.5.1.69; FDS-5. Cat No: EXWM-2806. | |
| M 25 | M 25 is a potent Smoothened (Smo) receptor antagonist with IC50 value of 5 nM. It inhibits the Hedgehog signaling pathway. It also inhibits Shh induced Gli luciferase reporter activity in Shh-light 2 cells. It antagonizes GSA-10 and SAG-mediated differentiation of the C3H10T1/2 cell line. Synonyms: M 25; M25; M-25; N-[[1-(2-Methoxyphenyl)-1H-indazol-5-yl]methyl]-2-propylpentanamide. Grades: ≥98% by HPLC. Molecular formula: C23H29N3O2. Mole weight: 379.50. | |
| Methyl linoleate | Methyl linoleate, a major active constituent of Sageretia thea fruit (HFSF), is a major anti-melanogenic compound. Methyl linoleate downregulates microphthalmia-associated transcription factor (MITF) and tyrosinase-related proteins [1]. Uses: Scientific research. Group: Natural products. CAS No. 112-63-0. Pack Sizes: 10 mM * 1 mL; 1 g; 5 g. Product ID: HY-N1481. | |
| Micronomicin | Micronomicin (Gentamicin C2b) is an aminoglycoside antibiotic, with antibacterial and bactericidal activities [1]. Uses: Scientific research. Group: Natural products. Alternative Names: Gentamicin C2b; Antibiotic XK-62-2; Sagamicin. CAS No. 52093-21-7. Pack Sizes: 100 mg. Product ID: HY-B1915. | |
| Micronomicin sulfate | Micronomicin is an aminoglycoside antibiotic originally isolated from Micromonospora sagamiensis var. nonreducans. It exhibits broad-spectrum activity against Gram-positive and Gram-negative activity. Synonyms: Antibiotic XK-62-2; Gentamicin C2b; Santemycin; Sagamicin. Grades: ≥95%. CAS No. 66803-19-8. Molecular formula: C20H43N5O11S. Mole weight: 561.65. | |
| Micronomicin sulfate | Micronomicin sulfate (Gentamicin C2b sulfate) is an aminoglycoside antibiotic isolated from Micromonospora. Micronomicin sulfate is a broad-spectrum antibiotic close to the gentamicin-type antibiotics, exhibits a high activity against Pseudomonas , Proteus , Klebsiella pneumoniae , Serratia , etc ( MIC =0.001-8.3 μg/ml) [1] [2]. Uses: Scientific research. Group: Natural products. Alternative Names: Gentamicin C2b sulfate; Antibiotic XK-62-2 sulfate; Sagamicin sulfate. CAS No. 66803-19-8. Pack Sizes: 25 mg; 50 mg; 100 mg. Product ID: HY-108307. | |
| Niclosamide | Niclosamide. Uses: For analytical and research use. Group: Pesticides & metabolites; pesticides & metabolites; api standards; pharmaceutical toxicology. Alternative Names: BAY 2353, Nasemo, Helmiantin, Zestocarp, Benzamide, 5-chloro-N-(2-chloro-4-nitrophenyl)-2-hydroxy-Salicylanilide, 2',5-dichloro-4'-nitro- (8CI), Cestocide, Phenasal, Mansonil, 5-Chloro-N-(2-chloro-4-nitrophenyl)-2-hydroxybenzamide, Radeverm, Sulqui, Yomesan, Lintex, 2-Chloro-4-nitrophenylamide-6-chlorosalicylic acid, N-(2-Chloro-4-nitrophenyl)-5-chlorosalicylamide, Iomesan, N-(2'-Chloro-4'-nitrophenyl)-5-chlorosalicylamide, WR 46234, Devermin, Bayer 2353, 2',5-Dichloro-4'-nitrosalicylanilide, Sagimid, NSC 178296, Cestocid, Fenasal, Vermitid, Vermitin, Fedal-Telmin, Mato, HL 2447, Tredemine, Niclocide, 5-Chloro-2'-chloro-4'-nitrosalicylanilide, 5-Chloro-N-(2'-chloro-4'-nitrophenyl)salicylamide, Niclosamide, 5-Chloro-N-(2-chloro-4-nitrophenyl)-2-hydroxybenzamide, 2-Hydroxy-5-chloro-N-(2-chloro-4-nitrophenyl)benzamide, Ruby, Utosamide, Devermine, Bayluscid,Niclosamide anhydrous. CAS No. 50-65-7. IUPAC Name: 5-chloro-N-(2-chloro-4-nitrophenyl)-2-hydroxybenzamide. Molecular formula: C13H8Cl2N2O4. Mole weight: 327.12. Catalog: APS50657. SMILES: Oc1ccc(Cl)cc1C(=O)Nc2ccc(cc2Cl)[N+](=O)[O-]. Format: Neat. | |
| Niclosamide monohydrate | Niclosamide Monohydrate is used for the treatment of most tapeworm infections by inhibiting DNA replication. It inhibits the TNF-induced NF-κB reporter activity in a dose- and time-dependent manner in U2OS cells. It also inhibits TNF-induced degradation of IκBα and relocation of p65 in a dose- and time-dependent manner in HL-60, Molm13, or AML primary cells. Synonyms: Niclocide monohydrate; BAY2353 monohydrate; BAY 2353 monohydrate; BAY-2353 monohydrate; Cestocid monohydrate; Sagimid monohydrate; Yomesan monohydrate. Grades: >98%. CAS No. 73360-56-2. Molecular formula: C13H10Cl2N2O5. Mole weight: 345.13. | |
| Palmatrubine | Palmatrubine is an alkaloid isolated from the herbs of Tinospora sagittata. Synonyms: Dibenzo[a,g]quinolizinium, 5,6-dihydro-9-hydroxy-2,3,10-trimethoxy-. Grades: >98%. CAS No. 16176-68-4. Molecular formula: C20H20NO4. Mole weight: 338.4. | |
| Patchouli Oil Heart 65 PA | Patchouli oils are produced by steam distillation of the dried leaves of Pogostemon Cablin. Indonesia is the largest producer of Patchouli Oil, contributing to over 80% of the global supply (1.000 - 1.200 MT). Van Aroma is the leading producer of Patchouli Oil. Patchouli blends well with Bergamot, Black Pepper, Clary Sage, Elemi, Frankincense, Geranium, Ginger, Lavender, Lemongrass, Myrrh, Neroli, Pine, Rose, Rosewood and Sandalwood. Uses: Cosmetic and Care. Group: Plant Extracts. INCI Names: Pogostemon Cablin Oil. Grades: FOOD GRADE. CAS No. 84238-39-1 ; 8014-09-3. Pack Sizes: 25 kgs Jerrycan, 200 kg Drums. Product ID: PL-305. Olfactive Profile: Woody, balsamic, earthy, camphor. EC No: 282-493-4. FEMA No: 2838. Origin: Indonesia. | New Jersey |
| Patchouli Oil Sulawesi Dark Min 28 PA Acid < 15 | Patchouli oils are produced by steam distillation of the dried leaves of Pogostemon Cablin. Indonesia is the largest producer of Patchouli Oil, contributing to over 80% of the global supply (1.000 - 1.200 MT). Van Aroma is the leading producer of Patchouli Oil. Patchouli blends well with Bergamot, Black Pepper, Clary Sage, Elemi, Frankincense, Geranium, Ginger, Lavender, Lemongrass, Myrrh, Neroli, Pine, Rose, Rosewood and Sandalwood. Uses: Cosmetic and Care, Fragrance Products. Group: Plant Extracts. INCI Names: Pogostemon Cablin Oil. Grades: FOOD GRADE. CAS No. 84238-39-1 ; 8014-09-3. Pack Sizes: 25 kgs Jerrycan, 200 kg Drums. Product ID: PL-109. Olfactive Profile: Earthy, camphoraceous, woody, minty, musky. EC No: 282-493-4. FEMA No: 2838. Origin: Indonesia. | New Jersey |
| Patchouli Oil Sulawesi Dark Min 29 PA Acid < 15 | Patchouli oils are produced by steam distillation of the dried leaves of Pogostemon Cablin. Indonesia is the largest producer of Patchouli Oil, contributing to over 80% of the global supply (1.000 - 1.200 MT). Van Aroma is the leading producer of Patchouli Oil. Patchouli blends well with Bergamot, Black Pepper, Clary Sage, Elemi, Frankincense, Geranium, Ginger, Lavender, Lemongrass, Myrrh, Neroli, Pine, Rose, Rosewood and Sandalwood. Uses: Cosmetic and Care, Essential Oils, Fragrances. Group: Plant Extracts. INCI Names: Pogostemon Cablin Oil. Grades: FOOD GRADE. CAS No. 84238-39-1. Pack Sizes: 25 kgs Jerrycan, 200 kg Drums. Product ID: PL-107. Olfactive Profile: Earthy, grounding, woody, minty, musky. EC No: 282-493-4. FEMA No: 2838. Origin: Indonesia. | New Jersey |
| Patchouli Oil Sulawesi Dark Min 29 PA Acid < 8 | Patchouli oils are produced by steam distillation of the dried leaves of Pogostemon Cablin. Indonesia is the largest producer of Patchouli Oil, contributing to over 80% of the global supply (1.000 - 1.200 MT). Van Aroma is the leading producer of Patchouli Oil. Patchouli blends well with Bergamot, Black Pepper, Clary Sage, Elemi, Frankincense, Geranium, Ginger, Lavender, Lemongrass, Myrrh, Neroli, Pine, Rose, Rosewood and Sandalwood. Uses: Cosmetic and Care, Fragrance Products. Group: Plant Extracts. INCI Names: Pogostemon Cablin Oil. Grades: FOOD GRADE. CAS No. 84238-39-1 ; 8014-09-3. Pack Sizes: 25 kgs Jerrycan, 200 kg Drums. Product ID: PL-106. Olfactive Profile: Earthy, camphoraceous, woody, minty, musky. EC No: 282-493-4. FEMA No: 2838. Origin: Indonesia. | New Jersey |
| Patchouli Oil Sulawesi Dark Min 30 PA Acid < 5 | Patchouli oils are produced by steam distillation of the dried leaves of Pogostemon Cablin. Indonesia is the largest producer of Patchouli Oil, contributing to over 80% of the global supply (1.000 - 1.200 MT). Van Aroma is the leading producer of Patchouli Oil. Patchouli blends well with Bergamot, Black Pepper, Clary Sage, Elemi, Frankincense, Geranium, Ginger, Lavender, Lemongrass, Myrrh, Neroli, Pine, Rose, Rosewood and Sandalwood. Uses: Cosmetic and Care, Fragrance Products. Group: Plant Extracts. INCI Names: Pogostemon Cablin Oil. Grades: FOOD GRADE. CAS No. 84238-39-1. Pack Sizes: 25 kgs Jerrycan, 200 kg Drums. Product ID: PL-105. Olfactive Profile: Earthy, camphoraceous, woody, minty, musky. EC No: 282-493-4. FEMA No: 2838. Origin: Indonesia. | New Jersey |
| Patchouli Oil Sulawesi Dark Min 30 PA Acid < 8 | Patchouli oils are produced by steam distillation of the dried leaves of Pogostemon Cablin. Indonesia is the largest producer of Patchouli Oil, contributing to over 80% of the global supply (1.000 - 1.200 MT). Van Aroma is the leading producer of Patchouli Oil. Patchouli blends well with Bergamot, Black Pepper, Clary Sage, Elemi, Frankincense, Geranium, Ginger, Lavender, Lemongrass, Myrrh, Neroli, Pine, Rose, Rosewood and Sandalwood. Uses: Cosmetic and Care, Essential Oils. Group: Plant Extracts. INCI Names: Pogostemon Cablin Oil. Grades: FOOD GRADE. CAS No. 84238-39-1 ; 8014-09-3. Pack Sizes: 25 kgs Jerrycan, 200 kg Drums. Product ID: PL-104. Olfactive Profile: Earthy, camphoraceous, woody, minty, musky. EC No: 282-493-4. FEMA No: 2838. Origin: Indonesia. | New Jersey |
| Patchouli Oil Sulawesi Iron Free Min 30 PA | Patchouli oils are produced by steam distillation of the dried leaves of Pogostemon Cablin. Indonesia is the largest producer of Patchouli Oil, contributing to over 80% of the global supply (1.000 - 1.200 MT). Van Aroma is the leading producer of Patchouli Oil. Patchouli blends well with Bergamot, Black Pepper, Clary Sage, Elemi, Frankincense, Geranium, Ginger, Lavender, Lemongrass, Myrrh, Neroli, Pine, Rose, Rosewood and Sandalwood. Uses: Cosmetic and Care, Essential Oils. Group: Plant Extracts. INCI Names: Pogostemon Cablin Oil. Grades: FOOD GRADE. CAS No. 84238-39-1 ; 8014-09-3. Pack Sizes: 25 kgs Jerrycan, 200 kg Drums. Product ID: PL-203. Olfactive Profile: Earthy, camphoraceous, woody, minty, musky. EC No: 282-493-4. FEMA No: 2838. Origin: Indonesia. | New Jersey |
| Patchouli Oil Sulawesi M.D. Min 30 PA | Patchouli oils are produced by steam distillation of the dried leaves of Pogostemon Cablin. Indonesia is the largest producer of Patchouli Oil, contributing to over 80% of the global supply (1.000 - 1.200 MT). Van Aroma is the leading producer of Patchouli Oil. Patchouli blends well with Bergamot, Black Pepper, Clary Sage, Elemi, Frankincense, Geranium, Ginger, Lavender, Lemongrass, Myrrh, Neroli, Pine, Rose, Rosewood and Sandalwood. Uses: Cosmetic and Care. Group: Plant Extracts. INCI Names: Pogostemon Cablin Oil. Grades: FOOD GRADE. CAS No. 84238-39-1 ; 8014-09-3. Pack Sizes: 25 kgs Jerrycan, 200 kg Drums. Product ID: PL-303. Olfactive Profile: Earthy, camphoraceous, woody, minty, musky. EC No: 282-493-4. FEMA No: 2838. Origin: Indonesia. | New Jersey |
| Patchouli Oil Sumatra Dark Min 30 PA | Patchouli oils are produced by steam distillation of the dried leaves of Pogostemon Cablin. Indonesia is the largest producer of Patchouli Oil, contributing to over 80% of the global supply (1.000 - 1.200 MT). Van Aroma is the leading producer of Patchouli Oil. Patchouli blends well with Bergamot, Black Pepper, Clary Sage, Elemi, Frankincense, Geranium, Ginger, Lavender, Lemongrass, Myrrh, Neroli, Pine, Rose, Rosewood and Sandalwood. Uses: Cosmetic and Care, Fragrance Products. Group: Plant Extracts. INCI Names: Pogostemon Cablin Oil. Grades: FOOD GRADE. CAS No. 84238-39-1 ; 8014-09-3. Pack Sizes: 25 kgs Jerrycan, 200 kg Drums. Product ID: PL-103. Olfactive Profile: Earthy, camphoraceous, woody, minty, musky. EC No: 282-493-4. FEMA No: 2838. Origin: Indonesia. | New Jersey |
| Patchouli Oil Sumatra Dark Min 32 PA | Patchouli oils are produced by steam distillation of the dried leaves of Pogostemon Cablin. Indonesia is the largest producer of Patchouli Oil, contributing to over 80% of the global supply (1.000 - 1.200 MT). Van Aroma is the leading producer of Patchouli Oil. Patchouli blends well with Bergamot, Black Pepper, Clary Sage, Elemi, Frankincense, Geranium, Ginger, Lavender, Lemongrass, Myrrh, Neroli, Pine, Rose, Rosewood and Sandalwood. Uses: Cosmetic and Care. Group: Plant Extracts. INCI Names: Pogostemon Cablin Oil. Grades: FOOD GRADE. CAS No. 84238-39-1 ; 8014-09-3. Pack Sizes: 25 kgs Jerrycan, 200 kg Drums. Product ID: PL-102. Olfactive Profile: Earthy, camphoraceous, woody, minty, musky. EC No: 282-493-4. FEMA No: 2838. Origin: Indonesia. | New Jersey |
| Patchouli Oil Sumatra Dark Premium Min 34 PA | Patchouli oils are produced by steam distillation of the dried leaves of Pogostemon Cablin. Indonesia is the largest producer of Patchouli Oil, contributing to over 80% of the global supply (1.000 - 1.200 MT). Van Aroma is the leading producer of Patchouli Oil. Patchouli blends well with Bergamot, Black Pepper, Clary Sage, Elemi, Frankincense, Geranium, Ginger, Lavender, Lemongrass, Myrrh, Neroli, Pine, Rose, Rosewood and Sandalwood. Uses: Cosmetic and Care. Group: Plant Extracts. INCI Names: Pogostemon Cablin Oil. Grades: FOOD GRADE. CAS No. 84238-39-1 ; 8014-09-3. Pack Sizes: 25 kgs Jerrycan, 200 kg Drums. Product ID: PL-101. Olfactive Profile: Earthy, camphoraceous, woody, minty, musky. EC No: 282-493-4. FEMA No: 2838. Origin: Indonesia. | New Jersey |
| Patchouli Oil Sumatra Iron Free Min 30 PA | Patchouli oils are produced by steam distillation of the dried leaves of Pogostemon Cablin. Indonesia is the largest producer of Patchouli Oil, contributing to over 80% of the global supply (1.000 - 1.200 MT). Van Aroma is the leading producer of Patchouli Oil. Patchouli blends well with Bergamot, Black Pepper, Clary Sage, Elemi, Frankincense, Geranium, Ginger, Lavender, Lemongrass, Myrrh, Neroli, Pine, Rose, Rosewood and Sandalwood. Uses: Cosmetic and Care. Group: Plant Extracts. INCI Names: Pogostemon Cablin Oil. Grades: FOOD GRADE. CAS No. 84238-39-1 ; 8014-09-3. Pack Sizes: 25 kgs Jerrycan, 200 kg Drums. Product ID: PL-202. Olfactive Profile: Earthy, camphoraceous, woody, minty, musky. EC No: 282-493-4. FEMA No: 2838. Origin: Indonesia. | New Jersey |
Our database is helping our users find suppliers everyday.
