Ascorbyl Palmitate

Base Information

  • PRODUCT:Ascorbyl Palmitate
  • CAS.:137-66-6
  • MF:C22H38O7
  • Molecular Weight:414.54
  • Purity:99%

Product Details

CAS: 137-66-6

MF: C22H38O7

Appearance: White to yellowish colored powder

Buy High Quality Ascorbyl Palmitate 137-66-6 On Stock

  • Molecular Formula:C22H38O7
  • Molecular Weight:414.54
  • Appearance/Colour:White to yellowish colored powder 
  • Vapor Pressure:3.32E-14mmHg at 25°C 
  • Melting Point:115-118 °C 
  • Refractive Index:22.5 ° (C=1, EtOH) 
  • Boiling Point:512.7 °C at 760 mmHg 
  • PKA:3.96±0.10(Predicted) 
  • Flash Point:164.4 °C 
  • PSA:113.29000 
  • Density:1.15 g/cm3 
  • LogP:4.62480 

L-Ascorbyl 6-palmitate(Cas 137-66-6) Usage

Description

Ascorbyl palmitate is a lipophilic derivative of ascorbic acid with antioxidant and antiproliferative activities. It scavenges hydroxyl radicals in cell-free assays. Ascorbyl palmitate (0.01%) reduces the rate of autoxidation of soybean, safflower, sunflower, peanut, and corn oil. It inhibits increases in epidermal ornithine decarboxylase activity and DNA synthesis induced by phorbol 12-myristate 13-acetate (TPA; ) in mice in a concentration-dependent manner when applied topically. Ascorbyl palmitate (0.8 and 4 μmol per 200 μl of acetone, applied topically) reduces the number of tumors per mouse and the percentage of mice with tumors in a mouse skin two-stage model of tumor formation initiated and promoted by 7,12-dimethylbenz[a]anthracene (DMBA) and TPA, respectively. Formulations containing ascorbyl palmitate have been used as antioxidants and preservatives in foods, pharmaceuticals, and cosmetics.

Chemical Properties

Ascorbyl palmitate is a white or yellowish-white solid with a soapy taste and a citrus-like odor. It is very slightly soluble in water but freely soluble in alcohol, animal oil, and vegetable oil. It melts at 107° to 117°C (around 234°F). Ascorbyl palmitate prevents oxidative rancidity development by quenching singlet oxygen. The ascorbic acid part of the molecule donates hydrogen (a reducing agent). This phenomenon is also called "oxygen scavenging".

Uses

Ascorbyl Palmitate is an ester formed from ascorbic acid and palmitic acid creating a fat soluble form of vitamin C. It is used as an antioxidant food additive. It is also used as a preservative and an anti-oxidant in cosmetic creams and lotions to prevent rancidity. Ascorbyl palmitate facilitates the incorporation of ingredients such as vitamins A, C, and D into cosmetic formulations. It has no known toxicity.

Definition

ChEBI: Ascorbyl palmitate is a fatty acid ester. It is derived from corn dextrose fermentation and palm oil. It is used as a food preservative and as an antioxidant in oils, fats, and pharmaceuticals.

Production Methods

Ascorbyl palmitate is prepared synthetically by the reaction of ascorbic acid with sulfuric acid followed by reesterification with palmitic acid.

Application

Ascorbyl Palmitate is an antioxidant formed by combining ascorbic acid with palmitic acid. ascorbic acid is not fat soluble but ascorbyl palmitate is, thus combining them produces a fat-soluble antioxidant. it exists as a white or yellowish white powder of citric- like odor. it is used as a preservative for natural oils, edible oils, colors, and other substances. it acts synergistically with alpha-tocopherol in oils/fats. it is used in peanut oil at a maximum level of 200 mg/kg individually or in combination.

General Description

A white or yellowish-white powder having a citrus-like odor. Mp 116–117°C; soluble in alcohol and in animal and vegetable oils; slightly soluble in water. Ascorbyl Palmitate is a lipophilic ascorbic acid derivative, used as an antioxidant in both food and cosmetics industries.

Pharmaceutical Applications

Ascorbyl palmitate is primarily used either alone or in combination with alpha tocopherol as a stabilizer for oils in oral pharmaceutical formulations and food products; generally 0.05% w/v is used. It may also be used in oral and topical preparations as an antioxidant for drugs unstable to oxygen. The combination of ascorbyl palmitate with alpha tocopherol shows marked synergism, which increases the effect of the components and allows the amount used to be reduced. The solubility of ascorbyl palmitate in alcohol permits it to be used in nonaqueous and aqueous systems and emulsions.

Biochem/physiol Actions

6-O-Palmitoyl-L-ascorbic acid possesses metastasis inhibitory and anti-tumor activity. Ascorbyl palmitate exhibits antioxidant activity by protecting the cell membranes from oxidative damage.

Safety Profile

When heated to decomposition it emits acrid smoke and irritating fumes.

Safety

Ascorbyl palmitate is used in oral pharmaceutical formulations and food products, and is generally regarded as an essentially nontoxic and nonirritant material. The WHO has set an estimated acceptable daily intake for ascorbyl palmitate at up to 1.25 mg/kg bodyweight. LD50 (mouse, oral): 25 g/kg LD50 (rat, oral): 10 g/kg

storage

Ascorbyl palmitate is stable in the dry state, but is gradually oxidized and becomes discolored when exposed to light and high humidity. In an unopened container, stored in a cool place, it has a shelf life of at least 12 months. During processing, temperatures greater than 658℃ should be avoided. The bulk material should be stored in an airtight container at 8–158℃, protected from light.

Incompatibilities

Incompatibilities are known with oxidizing agents; e.g. in solution oxidation is catalyzed by trace metal ions such as Cu2+ and Fe3+.

Regulatory Status

GRAS listed. Accepted for use as a food additive in Europe. Included in the FDA Inactive Ingredients Database (oral, rectal, topical preparations). Included in nonparenteral medicines licensed in the UK.

Who Evaluation

Evaluation year: 1973

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/h17,21,23,26-27H,2-16H2,1H3/t17-,21+/m0/s1

137-66-6 Relevant articles

Enzymatic synthesis of ascorbyl palmitate in ultrasound-assisted system: Process optimization and kinetic evaluation

Lerin, Lindomar A.,Feiten, Miriam C.,Richetti, Aline,Toniazzo, Geciane,Treichel, Helen,Mazutti, Marcio A.,Vladimir Oliveira,Oestreicher, Enrique G.,De Oliveira, Débora

, p. 988 - 996 (2011)

This work is focused on the optimization...

Effect of the alkyl chains and of the headgroups on the thermal behavior of ascorbic acid surfactants mixtures

Venturini, Chiara,Pomposi, Cristina,Ambrosi, Moira,Carretti, Emiliano,Fratini, Emiliano,Lo Nostro, Pierandrea,Baglioni, Piero

, p. 3053 - 3062 (2014)

The role of the alkyl chain length and o...

Lipase catalyzed ascorbyl palmitate synthesis under microwave irradiation

Costa, Ingrid C.R.,Sutili, Felipe K.,Da Silva, Gabriela V.V.,Leite, Selma G.F.,Miranda, Leandro S.M.,De Souza, Rodrigo O.M.A.

, p. 127 - 131 (2014)

The production of ascorbyl palmitate fro...

Antioxidative properties and enzymatic synthesis of ascorbyl FA esters

Viklund, Fredrik,Alander, Jari,Hult, Karl

, p. 795 - 799 (2003)

Efficient synthesis of unsaturated FA es...

High yields of ascorbyl palmitate by thermostable lipase-mediated esterification

Bradoo,Saxena,Gupta

, p. 1291 - 1295 (1999)

High yields of ascorbyl palmitate (6-O-p...

Enzymatic synthesis and anti-oxidative activities of plant oil-based ascorbyl esters in 2-methyltetrahydrofuran-containing mixtures

Hu, Ying-Dan,Zong, Min-Hua,Li, Ning

, p. 181 - 188 (2016)

Ascorbyl fatty acid esters are commercia...

Coagels from alkanoyl-6-O-ascorbic acid derivatives as drug carriers: Structure and rheology

Palma, Santiago,Jimenez-Kairuz, Alvaro,Fratoni, Laura,Lo Nostro, Pierandrea,Manzo, Ruben,Allemandi, Daniel

, p. 1271 - 1276 (2003)

6-O-Ascorbic acid alkanoates (ASCn, wher...

Green synthesis method of vitamin C higher fatty acid ester

-

Paragraph 0049-0063, (2021/03/13)

The invention discloses a green synthesi...

Preparation method of L-ascorbic acid-6-palmitate

-

Paragraph 0047-0050, (2017/03/14)

The invention discloses a preparation me...

A direct esterification method reaction solution from separation and purification method for vitamin C palmitate hydrochloride

-

Paragraph 0017-0022, (2017/03/08)

The invention relates to a method for se...

137-66-6 Process route

palmitic anhydride
623-65-4

palmitic anhydride

ascorbic acid
50-81-7,98966-42-8

ascorbic acid

Ascorbyl palmitate
137-66-6,924964-24-9

Ascorbyl palmitate

Conditions
Conditions Yield
With dmap; at 80 ℃; for 8h; Temperature; Reagent/catalyst;
99.45%
palmitic anhydride
623-65-4

palmitic anhydride

1-hexadecylcarboxylic acid
57-10-3

1-hexadecylcarboxylic acid

ascorbic acid
50-81-7,98966-42-8

ascorbic acid

Ascorbyl palmitate
137-66-6,924964-24-9

Ascorbyl palmitate

Conditions
Conditions Yield
1-hexadecylcarboxylic acid; ascorbic acid; With sulfuric acid; at 18 ℃; for 15h;
palmitic anhydride; at 28 ℃; for 20h; Temperature;
91.3%

137-66-6 Upstream products

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    1-hexadecylcarboxylic acid

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137-66-6 Downstream products

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