Lavandulyl Suppliers USA

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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. Creative Enzymes
(±)-Lavandulyl acetate (±)-Lavandulyl acetate can be isolated from the oil components of Lavandula angustifolia Mill [1]. Uses: Scientific research. Group: Natural products. CAS No. 25905-14-0. Pack Sizes: 5 mg; 10 mg. Product ID: HY-117419A. MedChemExpress MCE
2-Isopropenyl-5-methyl-4-hexenoic Acid Ethyl Ester 2-Isopropenyl-5-methyl-4-hexenoic Acid Ethyl Ester is an intermediate in the synthesis of (±)-Lavandulyl Acetate (L200000), a component of lavender oil. Group: Biochemicals. Grades: Highly Purified. CAS No. 1845-54-1. Pack Sizes: 10mg, 25mg. Molecular Formula: C12H20O2. US Biological Life Sciences. USBiological 10
Worldwide
Kushenol F (Sophoraflavanone G) Kushenol F (Sophoraflavanone G). Group: Biochemicals. Alternative Names: 2?,4?,5,7-Tetrahydroxy-6-lavandulylflavanone; Norkurarinone;34981-24-3. Grades: Plant Grade. CAS No. 97938-30-2. Pack Sizes: 10mg. Molecular Formula: C25H28O6, Molecular Weight: 424.485999999999. US Biological Life Sciences. USBiological 9
Worldwide
leachianone-G 2''-dimethylallyltransferase This membrane-bound enzyme is located in the plastids and requires Mg2+ for activity. The reaction forms the lavandulyl sidechain of sophoraflavanone G by transferring a dimethylallyl group to the 2'' position of another dimethylallyl group attached at postiion 8 of leachianone G. The enzyme is specific for dimethylallyl diphosphate as the prenyl donor, as it cannot be replaced by isopentenyl diphosphate or geranyl diphosphate. Euchrenone a7 (a 5-deoxy derivative of leachianone G) and kenusanone I (a 7-methoxy derivative of leachianone G) can also act as substrates, but more slowly. Along with EC 1.14.13.103 (8-dimethylallylnaringenin 2'-hydroxylase) and EC 2.5.1.70 (naringenin 8-dimethylallyltransferase), this enzyme forms part of the sophoraflavanone-G-biosynthesis pathway. Group: Enzymes. Synonyms: LG 2''-dimethylallyltransferase; leachianone G 2''-dimethylallyltransferase; LGDT. Enzyme Commission Number: EC 2.5.1.71. 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-2809; leachianone-G 2''-dimethylallyltransferase; EC 2.5.1.71; LG 2''-dimethylallyltransferase; leachianone G 2''-dimethylallyltransferase; LGDT. Cat No: EXWM-2809. Creative Enzymes

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