Catalogue Number
BN-O1606
Analysis Method
Specification
98%(HPLC)
Storage
-20℃
Molecular Weight
344.4
Appearance
Powder
Botanical Source
This product is isolated and purified from the herbs of Heracleum repula Franch.
Structure Type
Category
SMILES
CC1(C(OC(O1)(C)C)COC2=C3C(=CC4=C2OC=C4)C=CC(=O)O3)C
Synonyms
9-{[(4R)-2,2,5,5-Tetramethyl-1,3-dioxolan-4-yl]methoxy}-7H-furo[3,2-g]chromen-7-one/7H-Furo[3,2-g][1]benzopyran-7-one, 9-[[(4R)-2,2,5,5-tetramethyl-1,3-dioxolan-4-yl]methoxy]-
IUPAC Name
Density
1.2±0.1 g/cm3
Solubility
Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Flash Point
251.2±28.7 °C
Boiling Point
491.8±45.0 °C at 760 mmHg
Melting Point
InChl
InChl Key
YCWZUJWUYQAIBF-CYBMUJFWSA-N
WGK Germany
RID/ADR
HS Code Reference
Personal Projective Equipment
Correct Usage
For Reference Standard and R&D, Not for Human Use Directly.
Meta Tag
provides coniferyl ferulate(CAS#:64790-68-7) MSDS, density, melting point, boiling point, structure, formula, molecular weight etc. Articles of coniferyl ferulate are included as well.>> amp version: coniferyl ferulate
No Technical Documents Available For This Product.
28620483
The primary goal was to investigate the effects of l-carnitine on fuel efficiency, as an antioxidant, and for muscle recovery in Labrador retrievers. Dogs were split into two groups, with one group being supplemented with 250 mg/d of Carniking™ l-carnitine powder. Two experiments (Expt 1 and Expt 2) were performed over a 2-year period which included running programmes, activity monitoring, body composition scans and evaluation of recovery using biomarkers. Each experiment differed slightly in dog number and design: fifty-six v. forty dogs; one endurance and two sprint runs per week v. two endurance runs; and differing blood collection time points. All dogs were fed a low-carnitine diet in which a fixed amount was offered based on maintaining the minimum starting weight. Results from Expt 1 found that the carnitine dogs produced approximately 4000 more activity points per km compared with the control group during sprint (P = 0·052) and endurance runs (P = 0·0001). Male carnitine dogs produced half the creatine phosphokinase (CPK) following exercise compared with male control dogs (P = 0·05). Carnitine dogs had lower myoglobin at 6·69 ng/ml following intensive exercise compared with controls at 24·02 ng/ml (P = 0·0295). Total antioxidant capacity (TAC) and thiobarbituric acid reactive substance (TBARS) results were not considered significant. In Expt 2, body composition scans indicated that the carnitine group gained more total tissue mass while controls lost tissue mass (P = 0·0006) and also gained lean mass while the control group lost lean mass (P < 0·0001). Carnitine dogs had lower CPK secretion at 23·06 v. control at 28·37 mU/ml 24 h after post-run (P = 0·003). Myoglobin levels were lower in carnitine v. control dogs both 1 h post-run (P = 0·0157; 23·83 v. 37·91 ng/ml) and 24 h post-run (P = 0·0189; 6·25 v.13·5 ng/ml). TAC indicated more antioxidant activity in carnitine dogs at 0·16 mm v. control at 0·13 mm (P = 0·0496). TBARS were also significantly lower in carnitine dogs both pre-run (P = 0·0013; 15·36 v. 23·42 µm) and 1 h post-run (P = 0·056; 16·45 v. 20·65 µm). Supplementing l-carnitine in the form of Carniking™ had positive benefits in Labrador retrievers for activity intensity, body composition, muscle recovery and oxidative capacity.
l-Carnitine, Canine performance, Dog nutrition, Muscle recovery, Antioxidants, Fuel efficiency, Labrador retrievers
Utilisation of supplemented l-carnitine for fuel efficiency, as an antioxidant, and for muscle recovery in Labrador retrievers
Jessica L. Varney,1 J. W. Fowler,1 W. C. Gilbert,2 and C. N. Coon1,*
2017
22798829
In the title compound, C19H18O, the cyclohexene ring has an envelope conformation with the methine C atom on the flap. The phenyl and methylphenyl rings form a dihedral angle of 85.93 (11)°. The crystal packing is consolidated by van der Waals forces and weak C—H⋯π interactions.
5-(4-Methylphenyl)-3-phenylcyclohex-2-en-1-one
Shaaban K. Mohamed,a Mehmet Akkurt,b,* Antar A Abdelhamid,a Kuldip Singh,c and Omyma A. A. Abd Allahd
2012 Jul 1;
29850106
In the cation of the title salt, C20H19N2O+·Br−, the phenyl rings are inclined to one another by 38.38 (8)°, whereas the central phenyl ring and the pyridiniminium ring are almost perpendicular with a dihedral angle of 87.37 (9)°. The N+=C cationic double bond was verified by the shortened bond length of 1.337 (2) a. In the crystal, the Br− anion is linked to the cation by an N—H⋯Br hydrogen bond. C—H⋯O hydrogen bonds link adjacent pyridiniminium cations into inversion dimers with an R 2 2(18) graph-set motif. These dimers are stacked in a phenyl-phenyl T-shaped geometry through C—H⋯π interactions. A Hirshfeld surface analysis was conducted to verify the contributions of the different intermolecular interactions.
crystal structure, ionic liquids, pyridiniminium salt, hydrogen bonding, Hirshfeld surface analysis
Crystal structure and Hirshfeld surface analysis of a pyridiniminium bromide salt: 1-[2-([1,1′-biphenyl]-4-yl)-2-oxoethyl]-3-methyl-1,4-dihydropyridin-4-iminium bromide
S. N. Sheshadri,a Huey Chong Kwong,b C. S. Chidan Kumar,c,* Ching Kheng Quah,d B. P. Siddaraju,e M. K. Veeraiah,f Muhammad Aiman Bin Abd Hamid,d and Ismail Waradg,*
2018 May 1
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