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Panthenol

Panthenol structure

Panthenol 

structure
  • CAS No:

    16485-10-2

  • Formula:

    C9H19NO4

  • Chemical Name:

    Panthenol

  • Synonyms:

    2,4-dihydroxy-N-(3-hydroxypropyl)-3,3-dimethyl-,(+-)-Butanamide;4-dihydroxy-n-(3-hydroxypropyl)-3,3-dimethyl-(+-)-butanamid;4-dihydroxy-n-(3-hydroxypropyl)-3,3-dimethyl-(+-)-butyramid;4-dihydroxy-n-(3-hydroxypropyl)-3,3-dimethyl-(+/-)-butanamid;4-dihydroxy-n-(3-hydroxypropyl)-3,3-dimethyl-dl-butyramid;DL-2 4-DIHYDROXY-N-(3-HYDROXYPROPYL)-3 3-DIMETHYLBUTYRAMIDE;DL-N-PANTOYL-E-PROPANOLAMINE;DL-PANTOTHENOL

  • Categories:

    Cosmetic Ingredient  >  Antistatic

Description

DL-Panthenol is an intermediate of organic synthesis.


Panthenol (also called pantothenol) is the alcohol analog of pantothenic acid (vitamin B5), and is thus a provitamin of B5. In organisms it is quickly oxidized to pantothenic acid. It is a viscous transparent liquid at room temperature. Panthenol is used as a moisturizer and to improve wound healing in pharmaceutical and cosmetic products.Panthenol is a multi-functional active ingredient that would be useful in most skin care formulations. Its efficacy has been substantiated in numerous peer-reviewed journals. The biologically active form of Panthenol, D-panthenol (EU), is the stable alcohol analogue of vitamin B5, pantothenic acid (EU), and is quickly converted to vitamin B5 (pantothenate) in the body. Pantothenic acid is present in all living cells and acts as an essential nutritional component due to its role in the formation of acetyl-co-enzyme A in the early stages of metabolism. The main role of acetyl-co-enzyme A is to provide activated acetic acid into the citric acid cycle (Krebs Cycle). This produces carbon dioxide, water, and energy. Co-enzyme A also transfers to other molecules such as Nacetyl-glucosamine (EU) and acetylcholine (EU) to help in the production of steroids and the synthesis of fatty acids. Coenzyme A also helps the body detoxify foreign substances.

Panthenol Basic Attributes

205.25

205.25

1724945

240-540-6

759899|759127|302962

TSCA listed

DTXSID3044598

White to Off-White

29362400

Characteristics

89.79000

-0.9

white crystalline powder or light yellow liquid

1.166±0.06 g/cm3(Predicted)

66-69 °C (lit.)

118-120 °C(Press: 0.02 Torr)

246.3ºC

1.501

Soluble in water, ethanol, ether, chloroform, and propylene glycol.

-20ºC

0.004Pa at 25℃

mouse,LD50,intraperitoneal,10100mg/kg (10100mg/kg),Farmaco, Edizione Scientifica. Vol. 14, Pg. 43, 1959.

Non flammable

13.03±0.20(Predicted)

Inert atmosphere,Room Temperature

Safety Information

NONH for all modes of transport

3

Xn

26-37-45-36/37/39-22

ES4316500

Xn

Panthenol is most stable form of pantothenic acid in liquid products

36/37/38-48-41-37/38-20/21/22

Drug Information

(+)-2,4-dihydroxy-N-(3-hydroxypropyl)-3,3-dimethylbutyramide

Panthenol Use and Manufacturing

Uses

Vitamin B5 precursor, radioprotectant, antimalarial


Panthenol, the active form of panthenol, is enzymatically cleaved to form pantothenic acid (Vitamin B5), which is an essential component of Coenzyme A that acts as a cofactor in many enzymatic reactions that are important for protein metabolism in the epithelium.Due to its good penetration and high local concentrations, dexpanthanol is used in many topical products, such as ointments and lotions for treatment of dermatological conditions to relieve itching or promote healing. Dermatological effects of the topical use of dexpanthenol include increased fibroblast proliferation and accelerated re-epithelialization in wound healing. Furthermore, it acts as a topical protectant, moisturizer, and has demonstrated anti-inflammatory properties. The vitamin ingredient Panthenol is valued in skin and hair care applications for its moisturizing properties. It has anti-inflammatory effects and soothes irritated and sensitive skin. For hair care application it is known for its humectant properties and its ability to improve the resistance of hair to mechanical stress.


panthenol (pro-vitamin B5) acts as a penetrating moisturizer. Panthenol appears to stimulate cellular proliferation and aid in tissue repair. Studies indicate that when topically applied, panthenol penetrates the skin and gets converted into pantothenic acid, a B complex vitamin. Such action could possibly influence the skin’s natural resources of pantothenic acid. It imparts a nonirritant, non-sensitizing, moisturizing, and conditioning feel and promotes normal keratinization and wound-healing. Panthenol protects the skin against sunburn, provides relief for existing sunburn, and enhances the natural tanning process. Panthenol’s humectant character enables it to hold water in the product or attract water from the environment, resulting in a moisturizing effect. It enhances skin suppleness, and claims are that it also acts as an anti-inflammatory agent. It is considered a non-comedogenic raw material.


DL-Panthenol is used in the topical treatment of skin disorders, such as minor irritations and skin burns. Also used in the strengthening and treatment of hair.

Butanamide, 2,4-dihydroxy-N-(3-hydroxypropyl)-3,3-dimethyl-: ACTIVE

EPA Safer Chemical Functional Use Classes -> Skin Conditioning Agents|Safer Chemical Classes -> Green half-circle - The chemical is expected to be of low concern|Cosmetics -> Antistatic; Hair conditioning; Skin conditioning

Computed Properties

Molecular Weight:205.25
XLogP3:-0.9
Hydrogen Bond Donor Count:4
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:6
Exact Mass:205.13140809
Monoisotopic Mass:205.13140809
Topological Polar Surface Area:89.8
Heavy Atom Count:14
Complexity:182
Undefined Atom Stereocenter Count:1
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

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