Conditions | Yield |
---|---|
With Lipozyme TL IM In tert-Amyl alcohol at 40℃; Enzymatic reaction; | 100% |
With phenylboronic acid; dmap 1.) water, t-BuOH, 2.) t-BuOH, 4 days, 25 deg C; Yield given. Multistep reaction; |
Conditions | Yield |
---|---|
With dmap at 80℃; for 8h; Temperature; Reagent/catalyst; | 99.45% |
palmitic anhydride
1-hexadecylcarboxylic acid
ascorbic acid
Ascorbyl palmitate
Conditions | Yield |
---|---|
Stage #1: 1-hexadecylcarboxylic acid; ascorbic acid With sulfuric acid at 18℃; for 15h; Stage #2: palmitic anhydride at 28℃; for 20h; Temperature; | 91.3% |
Conditions | Yield |
---|---|
With molecular sieve; immobilized Candida antarctica lipase B (Novozym 435) In tert-Amyl alcohol at 60℃; for 52h; Product distribution; Further Variations:; reaction time; molar ratio of reaction partners; | 86% |
With Novozym 435 (Can-dida antarctica lipase immobilized on macroporous polyacrylicresin) at 70℃; for 1h; Temperature; Time; Solvent; Molecular sieve; Irradiation; | 71% |
With Candida antarctica lipase In tert-butyl alcohol at 70℃; for 2h; ultrasonic irradiation; | 25.07% |
Conditions | Yield |
---|---|
With Bulkholderia multivorans lipase-loaded alumina at 80℃; for 0.666667h; Microwave irradiation; Neat (no solvent); regioselective reaction; | 83% |
Conditions | Yield |
---|---|
With Lipozyme TL IM In tert-Amyl alcohol at 40℃; Enzymatic reaction; | 20% |
[(2S)-2-[(2R)-3,4-dibenzyloxy-5-oxo-2H-furan-2-yl]-2-hydroxyethyl] hexadecanoate
Ascorbyl palmitate
Conditions | Yield |
---|---|
With hydrogen; palladium on activated charcoal In ethanol under 3000.24 Torr; |
(R)-3,4-bis(benzyloxy)-5-((S)-2,2-dimethyl-1,3-dioxolan-4-yl)furan-2(5H)-one
Ascorbyl palmitate
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: aq. AcOH / methanol / 80 °C 2: pyridine; 4-dimethylaminopyridine / CH2Cl2 3: H2 / Pd/C / ethanol / 3000.24 Torr View Scheme |
(2R)-3,4-dibenzyloxy-2-[(1S)-1,2-dihydroxyethyl]-2H-furan-5-one
Ascorbyl palmitate
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: pyridine; 4-dimethylaminopyridine / CH2Cl2 2: H2 / Pd/C / ethanol / 3000.24 Torr View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 5 steps 1: AcCl 2: K2CO3 / dimethylformamide / Heating 3: aq. AcOH / methanol / 80 °C 4: pyridine; 4-dimethylaminopyridine / CH2Cl2 5: H2 / Pd/C / ethanol / 3000.24 Torr View Scheme |
5,6-O-isopropylidene-L-ascorbic acid
Ascorbyl palmitate
Conditions | Yield |
---|---|
Multi-step reaction with 4 steps 1: K2CO3 / dimethylformamide / Heating 2: aq. AcOH / methanol / 80 °C 3: pyridine; 4-dimethylaminopyridine / CH2Cl2 4: H2 / Pd/C / ethanol / 3000.24 Torr View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: pyridine; 4-dimethylaminopyridine / CH2Cl2 2: H2 / Pd/C / ethanol / 3000.24 Torr View Scheme |
Conditions | Yield |
---|---|
With Candida antarctica lipase B immobilized on acrylic resin In 2-methyltetrahydrofuran; tert-butyl alcohol at 50℃; for 24h; Molecular sieve; Green chemistry; Enzymatic reaction; |
Conditions | Yield |
---|---|
With Candida antarctica lipase B immobilized on acrylic resin In 2-methyltetrahydrofuran; tert-butyl alcohol at 50℃; for 36h; Catalytic behavior; Kinetics; Solvent; Reagent/catalyst; Molecular sieve; Green chemistry; Enzymatic reaction; |
Conditions | Yield |
---|---|
With Candida antarctica lipase B immobilized on acrylic resin In 2-methyltetrahydrofuran; tert-butyl alcohol at 50℃; for 24h; Molecular sieve; Green chemistry; Enzymatic reaction; |
Conditions | Yield |
---|---|
With Candida antarctica lipase B immobilized on acrylic resin In 2-methyltetrahydrofuran; tert-butyl alcohol at 50℃; for 24h; Molecular sieve; Green chemistry; Enzymatic reaction; |
acrolein
Ascorbyl palmitate
Tetrahydro-5'-hydroxy-furan-2'-spiro-3,5(1-hydroxy-2-O-hexadecanoyl-ethyl)-tetrahydro-furan-2,4-dion
Conditions | Yield |
---|---|
In ethanol for 96h; Ambient temperature; | 80% |
Conditions | Yield |
---|---|
Stage #1: Thioctic acid With chloroformic acid ethyl ester; triethylamine In dichloromethane at -15 - 20℃; for 2h; Stage #2: Ascorbyl palmitate With triethylamine In dichloromethane at -15 - 20℃; for 2h; | 71% |
bis(cyclopentadienyl)molybdenum(IV) dichloride
Ascorbyl palmitate
Conditions | Yield |
---|---|
With sodium hydroxide In water at 20℃; pH=10; Inert atmosphere; | 60% |
Ascorbyl palmitate
Conditions | Yield |
---|---|
In ethanol; water at 20℃; for 0.0833333h; | 47% |
Ascorbyl palmitate
Conditions | Yield |
---|---|
With strontium (III) chloride hexahydrate In ethanol; water at 20℃; for 0.0833333h; | 47% |
Conditions | Yield |
---|---|
Stage #1: Ascorbyl palmitate With potassium carbonate In tetrahydrofuran; dimethyl sulfoxide for 0.5h; Stage #2: 2-nitrophenylmethyl bromide In tetrahydrofuran; dimethyl sulfoxide for 70h; Inert atmosphere; | 41% |
di-tert-butyl dicarbonate
Ascorbyl palmitate
Conditions | Yield |
---|---|
With pyridine at 20℃; Cooling with ice; | 40% |
Conditions | Yield |
---|---|
Stage #1: Ascorbyl palmitate With potassium carbonate In tetrahydrofuran; dimethyl sulfoxide for 0.5h; Stage #2: 6-nitroveratrylbromide In tetrahydrofuran; dimethyl sulfoxide Inert atmosphere; | 40% |
Conditions | Yield |
---|---|
With pyridine In toluene at 20℃; for 48h; | A 20% B 37% |
Conditions | Yield |
---|---|
With pyridine In toluene at 20℃; Cooling with ice; | 30% |
Conditions | Yield |
---|---|
Stage #1: Ascorbyl palmitate With potassium carbonate In tetrahydrofuran; dimethyl sulfoxide at 20℃; for 0.166667h; Inert atmosphere; Cooling; Darkness; Stage #2: 2-nitrophenylmethyl bromide In tetrahydrofuran; dimethyl sulfoxide at 20℃; for 120h; Inert atmosphere; | A 22% B 3% |
Conditions | Yield |
---|---|
Michael reaction; |
Conditions | Yield |
---|---|
Michael reaction; |
Ascorbyl palmitate
L-dehydroascorbic acid 6-palmitate
Conditions | Yield |
---|---|
With iodine; sodium hydrogencarbonate In ethanol at 20℃; for 0.5h; |
Conditions | Yield |
---|---|
Michael reaction; |
The IUPAC name of Ascorbyl palmitate is [2-(4,5-dihydroxy-3-oxofuran-2-yl)-2-hydroxyethyl] hexadecanoate. With the CAS registry number 137-66-6, it is also named as L-Ascorbic acid, 6-hexadecanoate. The product's categories are Food & Feed Additives; Biochemistry; Sugar Acids; Sugars; Vitamin Derivatives; Vitamins; Vitamins and derivatives; Food Additives; Vitamin Ingredients, and the other registry numbers are 120398-58-5; 162872-43-7; 57233-83-7; 924964-24-9. Besides, it is white to yellowish colored powder, which should be stored in a cool and dry warehouse to prevent high temperature, light and oxidation. In addition, its molecular formula is C22H38O7 and molecular weight is 414.54.
The other characteristics of this product can be summarized as: (1)EINECS: 205-305-4; (2)ACD/LogP: 6.07; (3)# of Rule of 5 Violations: 1; (4)ACD/LogD (pH 5.5): 4.8; (5)ACD/LogD (pH 7.4): 3.08; (6)ACD/BCF (pH 5.5): 1294.89; (7)ACD/BCF (pH 7.4): 24.68; (8)ACD/KOC (pH 5.5): 2566.05; (9)ACD/KOC (pH 7.4): 48.91; (10)#H bond acceptors: 7; (11)#H bond donors: 3; (12)#Freely Rotating Bonds: 21; (13)Index of Refraction: 1.52; (14)Molar Refractivity: 109.62 cm3; (15)Molar Volume: 360.2 cm3; (16)Surface Tension: 50.4 dyne/cm; (17)Density: 1.15 g/cm3; (18)Flash Point: 164.4 °C; (19)Melting Point: 115-118 °C; (20)Enthalpy of Vaporization: 90.24 kJ/mol; (21)Boiling Point: 512.7 °C at 760 mmHg; (22)Vapour Pressure: 1.17E-12 mmHg at 25 °C.
Preparation and Uses of Ascorbyl palmitate: this chemical is an ester formed from Ascorbic acid and Palmitic acid creating a fat-soluble form of Vitamin C. Additionally, this chemical is used as a source of vitamin C. It is also used as an antioxidant food additive (E number E304).
When you are using this chemical, please be cautious about it as the following: it is irritating to eyes, respiratory system and skin. It is also harmful by inhalation, in contact with skin and if swallowed. In case of contact with eyes, please rinse immediately with plenty of water and seek medical advice. And you should wear suitable protective clothing.
People can use the following data to convert to the molecule structure.
(1)SMILES: OC=1[C@H](OC(=O)C=1O)[C@@H](O)COC(=O)CCCCCCCCCCCCCCC
(2)InChI: InChI=1/C22H38O7/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-18(24)28-16-17(23)21-19(25)20(26)22(27)29-21/h17,21,23,25-26H,2-16H2,1H3/t17-,21+/m0/s1
(3)InChIKey: QAQJMLQRFWZOBN-LAUBAEHRBD
(4)Std. InChI: InChI=1S/C22H38O7/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-18(24)28-16-17(23)21-19(25)20(26)22(27)29-21/h17,21,23,25-26H,2-16H2,1H3/t17-,21+/m0/s1
(5)Std. InChIKey: QAQJMLQRFWZOBN-LAUBAEHRSA-N
The toxicity data is as follows:
Organism | Test Type | Route | Reported Dose (Normalized Dose) | Effect | Source |
---|---|---|---|---|---|
guinea pig | LD50 | skin | > 3gm/kg (3000mg/kg) | International Journal of Toxicology. Vol. 18(Suppl, | |
mouse | LD50 | oral | 25gm/kg (25000mg/kg) | FAO Nutrition Meetings Report Series. Vol. 53A, Pg. 146, 1974. |
About|Contact|Cas|Product Name|Molecular|Country|Encyclopedia
Message|New Cas|MSDS|Service|Advertisement|CAS DataBase|Article Data|Manufacturers | Chemical Catalog
©2008 LookChem.com,License: ICP
NO.:Zhejiang16009103
complaints:service@lookchem.com Desktop View