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CAS No:555-10-2
MF:C10H16
Appearance:colorless or light-yellow transparent liquid
Specification:98.5%
Package:1/5/10/25kgs/drum
Supply Capacity:Tons
Synonyms:(±)-beta-Phellandrene; 3-Isopropyl-6-methylene-1-cyclohexene; 4-Isopropyl-1-methylene-2-cyclohexene; NSC 53044; beta-Phellandrene; beta-Phellandrene; 3-Isopropyl-6-methylene-1-cyclohexene;p-mentha-1(7),2-diene;β-phellandrene,1(7)-2-p-menthadiene;Cyclohexene, 3-methylene-6-(1-methylethyl)-;3-methylidene-6-propan-2-yl-cyclohexene;1(7),2-p-Menthadiene;3-Methylene-6-isopropylcyclohexene;6-Isopropyl-3-methylene-1-cyclohexene; Beta-Phellandrene,"BETA-PHELLANDRENE; 555-10-2; p-Mentha-1(7),2-diene; 2-p-Menthadiene; 3-Isopropyl-6-methylene-1-cyclohexene; Cyclohexene, 3-methylene-6-(1-methylethyl)-; PHELLANDRENE, BETA; 3-Methylene-6-(1-methylethyl)cyclohexene; 4-Isopropyl-1-methylene-2-cyclohexene; 3-methylidene-6-propan-2-ylcyclohexene; CHEBI:48741; NSC-53044; 2KK225M001; DTXSID4052215; DTXCID201079569; 209-081-9; 3-Isopropyl-6-methylenecyclohex-1-ene; .beta.-Phellandrene; b-phellandrene; beta-Phellandren; 3-methylidene-6-(propan-2-yl)cyclohex-1-ene; b-Phellandrene (stabilized with 0.1% Hydroquinone); UNII-2KK225M001; HSDB 4080; beta -phellandrene; EINECS 209-081-9; MFCD23701544; NSC 53044; Phellandrene, .beta.; Epitope ID:123895; SCHEMBL154149; CHEMBL444254; orb1689870; BETA-PHELLANDRENE [HSDB]; .BETA.-PHELLANDRENE [MI]; 3-Isopropyl-6-methylenecyclohexene; HY-N8573; NSC53044; (+/-)-.BETA.-PHELLANDRENE; AKOS016008994; FM71450; 3-Isopropyl-6-methylene-1-cyclohexene #; MS-22800; SY411876; 3-Methylene-6-(1-methylethyl)-Cyclohexene; DB-366528; 3-methylene-6-(1-methylethenyl)-cyclohexane; CS-0148637; NS00012811; C19818; F82843; EN300-2528048; Q19606727",136.230,C10H16,;
Applications:
(±)-beta-Phellandrene (CAS No. 555-10-2) is a naturally occurring monocyclic monoterpene found in a broad spectrum of essential oils, such as peppermint, eucalyptus, and ginger. This captivating aroma molecule delivers a fresh, peppery fragrance characterized by subtle citrus, herbal, and woody undertones. Due to its reactive chemical nature, it serves as a versatile building block for synthesizing various fine chemicals.
1. Fragrance Formulation: Used as a top or heart note to create fresh, spicy, or forest-themed scents in perfumes, colognes, and personal care products.
2. Flavor Enhancement: Extensively applied in the food industry to impart natural peppery, citrusy, or herbal flavors to beverages, confectionery, and baked goods.
3. Pharmaceutical Intermediates: Acts as a vital building block in medicinal chemistry for the synthesis of bioactive compounds and novel drug candidates.
4. Plant Protection & Bio-pesticides: Due to its inherent anti-fungal and insect-repellent properties, it is utilized as an ingredient or synergist in eco-friendly agricultural products.
5. Chemical Synthesis Monomer: Serves as a reactant in organic synthesis, particularly in Diels-Alder reactions, to construct complex polycyclic molecular architectures.