CAS 10605-09-1

Ascorbic acid 6-stearate

Description:

Ascorbic acid 6-stearate, with the CAS number 10605-09-1, is an ester formed from ascorbic acid (vitamin C) and stearic acid. This compound is characterized by its role as a non-ionic surfactant and emulsifier, often utilized in food, cosmetic, and pharmaceutical formulations. It exhibits good solubility in organic solvents while being less soluble in water, which can enhance the stability and bioavailability of ascorbic acid in various applications. Ascorbic acid 6-stearate is known for its antioxidant properties, contributing to the preservation of products by preventing oxidative degradation. Additionally, it can improve the texture and consistency of formulations, making it valuable in the development of creams, lotions, and dietary supplements. Its safety profile is generally favorable, but like all additives, it should be used within established guidelines to ensure consumer safety. Overall, ascorbic acid 6-stearate serves as a multifunctional ingredient, combining the benefits of vitamin C with the properties of fatty acids.

Formula: C₂₄H₄₂O₇

InChI: InChI=1S/C24H42O7/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-20(26)30-18-19(25)23-21(27)22(28)24(29)31-23/h19,23,25,27-28H,2-18H2,1H3/t19-,23+/m0/s1

InChI key: InChIKey=LITUBCVUXPBCGA-WMZHIEFXSA-N

SMILES: [C@@H](COC(CCCCCCCCCCCCCCCCC)=O)(O)[C@@]1(C(O)=C(O)C(=O)O1)[H]

Synonyms:

• 2-(3,4-Dihydroxy-5-Oxo-2,5-Dihydrofuran-2-Yl)-2-Hydroxyethyl Octadecanoate (Non-Preferred Name)
• 6-O-Stearylascorbic acid
• 6-O-octadecanoylhex-1-enofuranos-3-ulose
• <span class="text-smallcaps">L</span>-Ascorbic acid monostearate
• <span class="text-smallcaps">L</span>-Ascorbic acid, 6-octadecanoate
• <span class="text-smallcaps">L</span>-Ascorbic acid, 6-stearate
• <span class="text-smallcaps">L</span>-Ascorbyl 6-octadecanoate
• Ascorbic acid 6-stearate
• Ascorbyl 6-stearate
• Ascorbyl stearate
• E 305
• L-Ascorbic acid 6-octadecanoate
• Stearic acid, 6-ester with <span class="text-smallcaps">L</span>-ascorbic acid
• Vitamin C stearate
• L-Ascorbic acid monostearate
• Stearic acid, 6-ester with L-ascorbic acid

6-O-Stearoyl-L-ascorbic Acid

CAS: 10605-09-1

Formula: C₂₄H₄₂O₇

Purity: >95.0%(T)

Color and Shape: White to Light yellow powder to crystal

Molecular weight: 442.59

Ref: 3B-A0617

Ascorbyl Stearate

CAS: 10605-09-1

Vitamin c (ascorbic acid) and its derivatives

Formula: C₂₄H₄₂O₇

Color and Shape: Powder

Molecular weight: 442.29305

Ref: 45-1043149

(2S)-2-[(2R)-3,4-dihydroxy-5-oxo-2,5-dihydrofuran-2-yl]-2-hydroxyethyl octadecanoate

CAS: 10605-09-1

Formula: C₂₄H₄₂O₇

Purity: 98%

Color and Shape: Solid

Molecular weight: 442.5861

Ref: IN-DA003R7X

L-Ascorbic Acid 6-stearate

CAS: 10605-09-1

L-Ascorbic acid 6-stearate, a compound derived from L-ascorbic acid and stearic acid identified in K.

Formula: C₂₄H₄₂O₇

Color and Shape: Solid

Molecular weight: 442.60

Ref: TM-T83876

Ascorbyl stearate

CAS: 10605-09-1

Formula: C₂₄H₄₂O₇

Purity: ≥ 95.0%

Color and Shape: White crystalline powder

Molecular weight: 442.59

Ref: 7W-GX5049

L-Ascorbic acid 6-stearate

CAS: 10605-09-1

L-Ascorbic acid 6-stearate

Purity: 98%

Molecular weight: 442.59g/mol

Ref: 54-OR1043293

L-Ascorbic Acid 6-Stearate

CAS: 10605-09-1

Applications L-Ascorbic Acid 6-Stearate is used to specifically target anti-tumoral dehydrocrotonin nanoparticles.
References Frungillo, L., et al.: J. Pharm. Sci., 98, 4796-4807 (2009)

Formula: C₂₄H₄₂O₇

Color and Shape: Neat

Molecular weight: 442.59

Ref: TR-A786985

6-O-Stearoyl-l-ascorbic acid

CAS: 10605-09-1

6-O-Stearoyl-l-ascorbic acid is a derivative of ascorbic acid that has been shown to induce apoptosis in cervical cancer cells. The mechanism by which 6-O-stearoyl-l-ascorbic acid induces the death of cancer cells is still unclear. It may be associated with the formation of reactive oxygen species and lipid peroxidation, or the depletion of mitochondrial membrane potential, or the inhibition of glutamate pyruvate transaminase. 6-O-Stearoyl-l-ascorbic acid also has effects on skin tumor formation and radiation response in mice. This compound has been found to have physiological effects as well; it inhibits fetal bovine serum fatty acid synthesis and causes cellular transformation in vitro.

Formula: C₂₄H₄₂O₇

Purity: Min. 95%

Color and Shape: Powder

Molecular weight: 442.59 g/mol

Ref: 3D-FS163221