L-Caryophyllene

Product Details

CAS No:87-44-5

MF:C15H24

Appearance:colorless or light-yellow transparent liquid

Specification:98.5%

UN number:-

Package:1/5/10/25kgs/drum

Supply Capacity:KGS

Synonyms:2-Methylene-6,10,10-trimethyl bicyclo[7.2.0]undec-5-ene;BetaCarryophellene;β-caryophyllene,[1R-(1R,4E,9S)]-4,11,11-trimethyl-8-methylene-bicyclo[7.2.0]undec-4-ene,(E)-caryophyllene;Bicyclo7.2.0undec-4-ene, 4,11,11-trimethyl-8-methylene-, (1R,4E,9S)-;CARYOPHYLLENE, (-)-trans-(SG);HUMULENE, alpha-(SG);8-METHYLENE-4,11,11-TRIMETHYLBICYCLO-UNDEC-4-ENE;BETA-CARYPOPHYLLENE; BETA-CARYOPHYLLENE; Caryophyllene; (-)-trans-Caryophyllene; 87-44-5; L-Caryophyllene; trans-beta-caryophyllene; beta-Caryophyllen; (-)-Caryophyllene; FEMA No. 2252; (1R,4E,9S)-4,11,11-trimethyl-8-methylidenebicyclo[7.2.0]undec-4-ene; (-)-E-Caryophyllene; NSC-11906; BHW853AU9H; 8-Methylene-4,11,11-(trimethyl)bicyclo(7.2.0)undec-4-ene; Bicyclo(7.2.0)undec-4-ene, 8-methylene-4,11,11-trimethyl-, (E)-(1R,9S)-(-)-; CHEBI:63191; 8-Methylene-4,11,11-(trimethyl)bicyclo[7.2.0]undec-4-ene; (1R,4E,9S)-4,11,11-trimethyl-8-methylidenebicyclo(7.2.0)undec-4-ene; Bicyclo(7.2.0)undec-4-ene, 4,11,11-trimethyl-8-methylene-, (1R,4E,9S)-; Bicyclo[7.2.0]undec-4-ene, 8-methylene-4,11,11-trimethyl-, (E)-(1R,9S)-(-)-; RefChem:6628; (1R,9S)-4,11,11-trimethyl-8-methylidenebicyclo(7.2.0)undec-4-ene; 201-746-1; trans-Caryophyllene; (-)-beta-caryophyllene; (E)-Caryophyllene; (E)-beta-caryophyllene; (-)-(E)-Caryophyllene; .beta.-Caryophyllene; b-caryophyllene; .beta.-Caryophyllen; cariofileno; MFCD00075925; Beta-Caryophylene; trans-.beta.-Caryophyllene; DTXSID8024739; CHEBI:10357; (E)-beta-caryophylene; 1-CARYOPHYLLENE; .beta.-(E)-Caryophyllene; (1R,9S,E)-4,11,11-trimethyl-8-methylenebicyclo[7.2.0]undec-4-ene; Cannabinoid; E-Caryophyllene; P198906; g-Caryophyllene; ss-Caryophyllene; clove terpenes; (1S,9R)-6,10,10-trimethyl-2-methylenebicyclo[7.2.0]undec-5-ene; NSC 11906; (1R,4E,9S)-4,11,11-trimethyl-8-methylene-bicyclo[7.2.0]undec-4-ene; trans-(1R,9S)-4,11,11-trimethyl-8-methylenebicyclo[7.2.0]undec-4-ene; E-.beta.-caryophyllene; .beta.-Caryophyllene, (-); caryophilene; Tincturoid; NSC11906; Caryophyllene B; Caryophyllene hg; beta-cariofillene; cb2 receptor; trans-caryphynene; transcaryophyllene; beta-caryophillene; (E)-caryophylene; |_-Caryophyllene; Bicyclo[7.2.0]undec-4-ene, 4,11,11-trimethyl-8-methylene-, [1R-(1R*,4E,9S*)]-; trans caryophyllene; caryophyllene 917; E-beta-caryophyllene; CAROPYLLENE; Caryophyllene, (E); (beta)-Caryophyllene; 02 - Terpenes; beta-(e)-caryophyllene; Eugenol EP Impurity A; beta-trans-caryophyllene; clove terpene derivative; (-)-trans caryophyllene; (?)-trans-Caryophyllene; caryophyllene beta natural; beta-Caryophyllene, 97%; CARYOPHYLLENE [MI]; .beta.-trans-Caryophyllene; (-)-I(2)-caryophyllene; 12 - Analysis of terpenes; |A-Caryophyllene (Standard); |?-Caryophyllene (Standard); Bicyclo[7.2.0]undec-4-ene, 4,11,11-trimethyl-8-methylene-; SCHEMBL113830; beta-Caryophyllene - min 98%; CHEMBL445740; DTXCID304739; (E)-beta-caryophyllene (BCP); BETA-CARYOPHYLLENE [FCC]; GTPL13282; HY-N1415R; BETA-CARYOPHYLLENE [INCI]; GLXC-14878; (-)-(E)-Caryophyllene(Standard); HY-N1415; .BETA.-CARYOPHYLLENE [FHFI]; Eugenol EP Impurity A (Free Base); Tox21_301497; 11CAR7501; BDBM50529607; AKOS024283988; EBC-618473; LMPR0103120001; beta-Caryophyllene, >=80%, FCC, FG; CAS-87-44-5; NCGC00142620-01; NCGC00255159-01; AC-37990; FC138498; FC164087; ST072181; SY060846; [7.2.0]undec-4-ene, (E)-caryophyllene; Eugenol EP Impurity A; (-)-Caryophyllene; (-)-trans-Caryophyllene, analytical standard; CS-0016839; NS00079049; C09629; beta-Caryophyllene 2000 microg/mL in Acetonitrile; F576574; Q421614; BRD-K26878113-001-01-6; (-)-trans-Caryophyllene, >=98.5% (sum of enantiomers, GC); bicyclo[7.2.0]undec-4-ene, 4,11,11-trimethyl-8-methylene; (1R,4E,9S)-4,11,11-TRIMETHYL-8-METHYLENEBICYCLO(7.2.0)UNDEC-4-ENE; 4,11,11-trimethyl-8-methylene-,[1R-(1R*,4E,9S*)]-bicyclo [7.2.0]undec-4-ene; 8-Methylene-4,11,11-(trimethyl)bicyclo(7.2.0)undec-4-ene, (1R,4E,9S)-; Bicyclo[7.2.0]undec-4-ene, 4,11,11-trimethyl-8-methylene-, (E)-(1R,9S)-(-)-; Bicyclo[7.2.0]undec-4-ene, 4,11,11-trimethyl-8-methylene-, [1R- (1R*,4E,9S*)]-

Product application:L-Caryophyllene,87-44-5,Beta-Caryophyllene,(-)-beta-Caryophyllene,trans-Caryophyllene,Natural beta-caryophyllene,Bicyclo[7.2.0]undec-4-ene derivative,Food grade caryophyllene,FEMA 2252,Flavoring agent,Cosmetic grade caryophyllene,Natural soothing active,Anti-inflammatory sesquiterpene,Woody spicy fragrance ingredient,Perfume fixative,Natural terpene hydrocarbon,Low peroxide value caryophyllene,High purity Beta-Caryophyllene 95%,CAS 87-44-5 supplier,L-Caryophyllene manufacturer China,Suzhou Health Chemicals natural aroma ingredients,Beta-Caryophyllene wholesale bulk export

 

L-Caryophyllene is widely utilized across savory and spicy food and beverage flavoring compounding, fine luxury perfumery and fragrance fixative formulation, dermatological barrier soothing and anti-irritant skin therapy development, oral dentifrice freshening engineering, and natural pharmaceutical process synthesis sectors. In flavor chemistry and culinary formulating science, universally recognized in global food regulations as Beta-Caryophyllene and FEMA 2252, it serves as an indispensable natural sesquiterpene hydrocarbon conferring warm, dry, woody, and clove-pepper aromatic nuances with subtle resinous undertones across seasoning blends, processed meats, bakery confections, and functional beverages; in functional perfumery and personal care scent architecture, its balanced molecular weight delivers low volatility and superior fixative capability, anchoring top and middle notes while imparting long-lasting woody elegance in prestige colognes, personal cleansing gels, and trichological hair oils; in cosmetic dermatology and dermal biology, its lipophilic bicyclic framework readily integrates into the stratum corneum where it modulates inflammatory cellular pathways and scavenges oxidative free radicals, delivering skin-calming, redness-reducing, and barrier-soothing benefits to sensitive, stressed, and post-environmental exposure skin profiles; furthermore, in natural products chemistry and fine organic synthesis, L-Caryophyllene provides reliable bicyclic reactivity and stereochemical fidelity for assembling caryophyllene oxide derivatives and bioactive synthons across commercial manufacturing operations.