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Vitamin A palmitate

CAS No.
79-81-2
Chemical Name:
Vitamin A palmitate
Synonyms
RETINYL PALMITATE;RETINOL PALMITATE;Vitamin a Palmitate Oil;Vitamin A Palmitate Powder;VITAMIN A PALMITATE 1.7 MIU;VitaminAPalmitateinOil;Dry Vitamin A Palmitate;Helianthus Annuus Seed Oil;Retinylpalmitat;VITAMIN A PALMITATE Liquid
CBNumber:
CB0406543
Molecular Formula:
C36H60O2
Molecular Weight:
524.86
MDL Number:
MFCD00019414
MOL File:
79-81-2.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-08-25 20:17:46

Vitamin A palmitate Properties

Melting point 28-29℃
Boiling point 546.51°C (rough estimate)
Density 0.9668 (rough estimate)
refractive index 1.5250 (estimate)
Flash point 194℃
storage temp. 2-8°C
solubility Chloroform (Slightly), Ethyl Acetate (Slightly), Methanol (Very Slightly)
form oil
pka -7
Specific Gravity 0.90~0.93 (20℃)
color Light Yellow to Yellow
biological source synthetic (organic)
Water Solubility Soluble in chloroform, ether, and vegetable oils. Insoluble in water.
Merck 13,10073
BRN 1917366
Specific Activity ~1,800,000USP units/g
BCS Class 4
Stability Light Sensitive
Major Application cleaning products
cosmetics
food and beverages
personal care
pharmaceutical (small molecule)
vitamins, nutraceuticals, and natural products
Cosmetics Ingredients Functions SKIN CONDITIONING - MISCELLANEOUS
InChIKey VYGQUTWHTHXGQB-YFAKFODJSA-N
SMILES O(C\C=C(/C)\C=C\C=C(/C)\C=C\C1=C(CCCC1(C)C)C)C(=O)CCCCCCCCCCCCCCC
LogP 15.51 at 25℃
CAS DataBase Reference 79-81-2(CAS DataBase Reference)
Substances Added to Food (formerly EAFUS) VITAMIN A PALMITATE
FDA 21 CFR 310.545; 582.5936
SCOGS (Select Committee on GRAS Substances) Vitamin A palmitate
NCI Dictionary of Cancer Terms retinyl palmitate
FDA UNII 1D1K0N0VVC
NIST Chemistry Reference Vitamin a palmitate(79-81-2)
EPA Substance Registry System Retinol, hexadecanoate (79-81-2)
UNSPSC Code 85151701
NACRES NA.79

SAFETY

Risk and Safety Statements

Symbol(GHS)  Health Hazard (GHS08)
GHS08
Signal word  Danger
Hazard statements  H360D-H412
Precautionary statements  P202-P273-P280-P308+P313-P405-P501
PPE Eyeshields, Gloves, type ABEK (EN14387) respirator filter
Hazard Codes  T,Xn,F
Risk Statements  63-53-61-11
Safety Statements  53-23-36/37/39-45-36/37-16-60
RIDADR  UN1170 - class 3 - PG 2 - Ethanol, solution
WGK Germany  3
RTECS  VH6860000
8-10-23
TSCA  TSCA listed
HS Code  29362100
Storage Class 6.1C - Combustible acute toxic Cat.3
toxic compounds or compounds which causing chronic effects
Hazard Classifications Aquatic Chronic 3
Repr. 1B
Toxicity LD50 (10 day) in mice, rats (mg/kg): 6060, 7910 orally (Kamm)
REACH Registrations Active

Vitamin A palmitate price More Price(33)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 46959-U Retinol palmitate analytical standard 79-81-2 100mg $38.5 2026-04-30 Buy
Sigma-Aldrich 1602502 Retinyl palmitate United States Pharmacopeia (USP) Reference Standard 79-81-2 4x50mg $511 2026-04-30 Buy
Cayman Chemical 23796 Retinyl Palmitate ≥95% 79-81-2 5g $69 2026-04-30 Buy
Cayman Chemical 23796 Retinyl Palmitate ≥95% 79-81-2 10g $120 2026-04-30 Buy
Cayman Chemical 23796 Retinyl Palmitate ≥95% 79-81-2 25g $248 2026-04-30 Buy
Product number Packaging Price Buy
46959-U 100mg $38.5 Buy
1602502 4x50mg $511 Buy
23796 5g $69 Buy
23796 10g $120 Buy
23796 25g $248 Buy

Vitamin A palmitate Chemical Properties,Uses,Production

Chemical Properties

95.0-100.5% Absorbance @325 nm ≥0.85%

Uses

antihypertensive

Uses

all-trans-Retinyl Palmitate is an ester derivative of Retinol (R252000). all-trans-Retinyl Palmitate is used as a vitamin supplement in the treatment of Vitamin A deficiency. all-trans-Retinyl Palmita te is used as an antioxidant and a source of vitamin A added to low fat milk and other dairy products. all-trans-Retinyl Palmitate is also a constituent of some topically applied skin care products

Uses

retinyl palmitate is a skin conditioner. This retinoid is considered a milder version of retinoic acid, given its conversion properties. once on the skin, it converts to retinol, which in turn converts to retinoic acid. Physiologically, it is credited with increasing R epidermal thickness, stimulating the production of more epidermal protein, and increasing skin elasticity. Cosmetically, retinyl palmitate is used to reduce the number and depth of fine lines and wrinkles, and prevent skin roughness resulting from uV exposure. Secondary reactions such as erythema, dryness, or irritation are not associated with retinyl palmitate. It is even more effective when used in combination with glycolic acid because it achieves greater penetration. In the united States, its maximum usage level in cosmetic formulations is 2 percent. Retinyl palmitate is the ester of retinol and palmitic acid.

Uses

vitamin A palmitate is known as a skin “normalizer.” It acts as an antikeratinizing agent, helping the skin stay soft and plump, and improving its water-barrier properties. Because of its impact on the skin’s water-barrier properties, it is useful against dryness, heat, and pollution. It is also an anti-oxidant and is suggested for use in sunscreens. Clinical studies with vitamin A palmitate indicate a significant change in skin composition, with increases in collagen, DnA, skin thickness, and elasticity. Vitamin A palmitate’s stability is superior to retinol.

Definition

ChEBI: All-trans-retinyl palmitate is an all-trans-retinyl ester obtained by formal condensation of the carboxy group of palmitic (hexadecanoic acid) with the hydroxy group of all-trans-retinol. It is used in cosmetic products to treat various skin disorders such as acne, skin aging, wrinkles, dark spots, and also protect against psoriasis. It has a role as an Escherichia coli metabolite, a human xenobiotic metabolite and an antioxidant. It is a retinyl palmitate and an all-trans-retinyl ester. It is functionally related to an all-trans-retinol.

General Description

Certified pharmaceutical secondary standards for application in quality control provide pharma laboratories and manufacturers with a convenient and cost-effective alternative to pharmacopeia primary standards.
Retinyl palmitate belongs to a category of compounds called retinoids, which are chemically similar to vitamin A. It exhibits a beneficial effect on vision, skin and immune function, inhibits cell proliferation and prevents cancer. It is an important dietary as well as a therapeutic compound.

Flammability and Explosibility

Non flammable

Biochem/physiol Actions

Vitamin A palmitate is widely used in pharmaceutical applications. It is also extensively used in cosmetic formulations due to its beneficial effects on the appearance of skin and anti-oxidant properties. Vitamin A palmitate acts as a teratogen and affect vertebrate embryogenesis and regeneration. It is added as a source of vitamin A in low fat and skim milks. Vitamin A palmitate acts as a chemopreventive or antineoplastic agent.
Review: Vitamin A metabolism.

Side effects

Vitamin A palmitate is fat-soluble and is stored in the body's fatty tissue. Therefore, excessive levels of vitamin A palmitate can lead to toxicity and liver disease. This is more likely to occur when taking supplements than when consuming them from food. People with liver disease should not take vitamin A palmitate supplements. Excessive doses of vitamin A supplements have been linked to birth defects, including malformations of the eyes, lungs, skull and heart. They are not recommended for pregnant women. Regular high doses of vitamin A letter source can lead to depression, dry skin, and muscle and joint pain.

Safety Profile

Mildly toxic by ingestion. An experimental teratogen. Experimental reproductive effects. Human mutation data reported. When heated to decomposition it emits acrid smoke and irritating fumes.

Synthesis

Methyl palmitate

112-39-0

Retinyl acetate

127-47-9

Vitamin A palmitate

79-81-2

Synthesis of (2E,4E,6E,8E)-3,7-dimethyl-9-(2,6,6-trimethylcyclohex-1-en-1-yl)nona-2,4,6,8-tetraen-1-yl acetate from methyl palmitate and (2E,4E,6E,8E)-3,7-dimethyl-9-(2,6,6-trimethylcyclohex-1-en-1-yl)nona-2,4,6, 8-tetraen-1-yl palmitate in the following general procedure: 3000 kg of vitamin A acetate (compound of formula Ia) in crystalline form and 2750 kg of methyl palmitate (compound of formula Ia) were added to the reactor. Subsequently, 10 kg of sodium hydroxide was dissolved in about 60 liters of methanol and this solution was added to the above mixture. The reaction mixture was heated to 55°C and the system pressure was reduced to 1500-2200 Pascal. The reaction lasted for about 3 hours, during which time the main by-product, methyl acetate, was continuously removed by distillation. Reaction termination was achieved by addition of water and carbon dioxide. Finally, the target product vitamin A palmitate (compound of formula IIIa) was isolated from the reaction solution by extraction in 96% yield.

Purification Methods

The palmitate is separated from retinol by column chromatography on water-deactivated alumina with hexane containing a very small percentage of acetone. It is also chromatographed on TLC silica gel G, using pet ether/isopropyl ether/acetic acid/water (180:20:2:5) or pet ether/acetonitrile/acetic acid/water (190:10:1:15) to develop the chromatogram. It is then recrystallised from propylene at low temperature (below -47o). [Beilstein 6 IV 4135.]

References

[1] Patent: WO2014/23772, 2014, A1. Location in patent: Page/Page column 9

Vitamin A palmitate Preparation Products And Raw materials

Global( 547)Suppliers
Supplier Tel Email Country ProdList Advantage
Beijing PUXI Technology Co., Ltd 400-808-7372 13161114455 1718638899@qq.com China 4994 58
Spec-Chem Industry Inc. 025-84523390 13505162978 sc@specchemind.com China 123 58
Wuhan Fortuna Chemical Co., Ltd 027-59207852 13308628970 buy@fortunachem.com China 2698 58
Kono Chem Co.,Ltd 029-86107037 15829389671 info@konochemical.com China 410 55
Hubei Weideli Chemical Reagent Co.,Ltd. 181-6332-1995 18062128043 18163321995@163.com China 4811 58
Taizhou Yuxin Biotechnology Co., Ltd., +86-0576--88902229 +86-13968687450 yuxin@yuxchem.com China 190 58
J & K SCIENTIFIC LTD. 18210857532 18210857532 jkinfo@jkchemical.com China 96815 76
3B Pharmachem (Wuhan) International Co.,Ltd. 18930552037 3bsc@sina.com China 15813 69
Wuhan Wei Shunda Technology Development Co., Ltd. 86-027-88774375 mwmwhot@163.com China 233 65
Chemsky(shanghai)International Co.,Ltd. 021-50135380 shchemsky@sina.com China 32273 50

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