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Panthenol, dl-panthenol, 16485-10-2 ,Dexpanthenol, 81-13-0, lopan, Cozyme, Motilyn, Panyonyl, Bepantol, Intrapan, Pantenyl, Bepanthen, Panthoderm, Bepanthene, pantothenol

Panthenol, dl-panthenol, 16485-10-2 ,Dexpanthenol, 81-13-0, lopanCozymeMotilynPanyonylBepantolIntrapanPantenylBepanthenPanthodermBepanthenepantothenol

dl-panthenol

CAS: 16485-10-2

Molecular Formula: C9H19NO4

Names and Identifiers

Name dl-panthenol
Synonyms Panthenol
DL-PANTHENOL
dl-panthenol
D,L-Panthenol
dl-pantothenyl alcohol
(+-)-pantothenyl alcohol
DL-N-PANTOYL-E-PROPANOLAMINE
2,4-dihydroxy-N-(3-hydroxypropyl)-3,3-dimethylbutanamide
4-dihydroxy-n-(3-hydroxypropyl)-3,3-dimethyl-dl-butyramid
4-dihydroxy-n-(3-hydroxypropyl)-3,3-dimethyl-(+-)-butyramid
4-dihydroxy-n-(3-hydroxypropyl)-3,3-dimethyl-(+-)-butanamid
DL-2 4-DIHYDROXY-N-(3-HYDROXYPROPYL)-3 3-DIMETHYLBUTYRAMIDE
2,4-dihydroxy-N-(3-hydroxypropyl)-3,3-dimethyl-,(+-)-Butanamide
CAS 16485-10-2
EINECS 240-540-6
InChI InChI=1/C9H19NO4/c1-9(2,6-12)7(13)8(14)10-4-3-5-11/h7,11-13H,3-6H2,1-2H3,(H,10,14)
InChIKey SNPLKNRPJHDVJA-UHFFFAOYSA-N

Physico-chemical Properties

Molecular Formula C9H19NO4
Molar Mass 205.25
Density 1.166±0.06 g/cm3(Predicted)
Melting Point 66-69 °C (lit.)
Boling Point 118-120 °C(Press: 0.02 Torr)
Specific Rotation(α) 0°(c=5, H2O)
Flash Point 246.3°C
Water Solubility Soluble in water, ethanol, ether, chloroform, and propylene glycol.
Solubility Acetonitrile (Slightly), DMSO (Slightly), Methanol (Slightly)
Vapor Presure 0.004Pa at 25℃
Appearance White crystal
Color White to Off-White
Merck 14,2947
BRN 1724945
pKa 13.03±0.20(Predicted)
Storage Condition Inert atmosphere,Room Temperature
Sensitive Hygroscopic
Refractive Index 1.501
MDL MFCD00002944
Physical and Chemical Properties White crystalline hygroscopic powder. Soluble in water, ethanol, methanol and propylene glycol, soluble in chloroform and ether, slightly soluble in glycerol, insoluble in vegetable oil, mineral oil and fat.

Risk and Safety

Hazard Symbols Xn - Harmful
Harmful
Risk Codes R36/37/38 - Irritating to eyes, respiratory system and skin.
R48 - Danger of serious damage to health by prolonged exposure
R41 - Risk of serious damage to eyes
R37/38 - Irritating to respiratory system and skin.
R20/21/22 - Harmful by inhalation, in contact with skin and if swallowed.
Safety Description S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S37 - Wear suitable gloves.
S45 - In case of accident or if you feel unwell, seek medical advice immediately (show the label whenever possible.)
S36/37/39 - Wear suitable protective clothing, gloves and eye/face protection.
S22 - Do not breathe dust.
WGK Germany 3
RTECS ES4316500
FLUKA BRAND F CODES 3
TSCA Yes
HS Code 29362400

Reference Information

LogP -1.02 at 22℃
traits provitamin B5 is a white crystalline hygroscopic powder. Provitamin B5 can promote the metabolism of human protein, fat and sugar, protect skin and mucous membrane, improve hair color and luster, and prevent the occurrence of diseases.
properties D-panthenol is easily soluble in water, ethanol, methanol and propylene glycol, soluble in chloroform and ether, slightly soluble in glycerin, insoluble in vegetable oil, mineral oil and fat.
identification test is the same as the identification test of "D-panthenol (01011).
content analysis is the same as "D-panthenol (01011).
toxicity GRAS(FDA § 182.5580,2000).
use limit is limited to GMP (FDA 182.5580,2000).
use pharmaceutical intermediates.

Dexpanthenol

CAS: 81-13-0

Molecular Formula: C9H19NO4

Names and Identifiers

Name Dexpanthenol
Synonyms Ilopan
Cozyme
Motilyn
Panyonyl
Bepantol
Intrapan
Pantenyl
Bepanthen
Panthoderm
Bepanthene
pantothenol
D-Panthenol
Alcopan-250
Dexpanthenol
(+)-Panthenol
pantothenylol
pantothenyl alcohol
N-pantoyl-3-propanolamine
Butanamide, 2,4-dihydroxy-N-(3-hydroxypropyl)-3,3-dimethyl-
(R)-2,4-Dihydroxy-N-(3-hydroxypropyl)-3,3-dimethylbutanamide
4-dihydroxy-n-(3-hydroxypropyl)-3,3-dimethyl-d-(+)-butyramid
(2S)-2,4-dihydroxy-N-(3-hydroxypropyl)-3,3-dimethylbutanamide
(2R)-2,4-dihydroxy-N-(3-hydroxypropyl)-3,3-dimethylbutanamide
4-dihydroxy-n-(3-hydroxypropyl)-3,3-dimethyl-(theta)-butanamid
Butanamide, 2,4-dihydroxy-N-(3-hydroxypropyl)-3,3-dimethyl-, (R)-
D(+)-ALPHA,GAMMA-DIHYDROXY-N-[3-HYDROXYPROPYL]-BETA,BETA-DIMETHYLBUTYRAMIDE
CAS 81-13-0
EINECS 201-327-3
InChI InChI=1/C9H19NO4/c1-9(2,6-12)7(13)8(14)10-4-3-5-11/h7,11-13H,3-6H2,1-2H3,(H,10,14)/t7-/m1/s1
InChIKey SNPLKNRPJHDVJA-ZETCQYMHSA-N

Physico-chemical Properties

Molecular Formula C9H19NO4
Molar Mass 205.25
Density 1.20 g/mL at 20 °C (lit.)
Melting Point 64~69℃
Boling Point 118-120 °C (2.7 mmHg)
Specific Rotation(α) 30.5 º (c=5, H2O on anh. sub)
Flash Point 118-120°C/0.02m
Water Solubility soluble
Solubility Soluble in water, ethanol, methanol, chloroform, slightly soluble in ether. Insoluble in fat and oil.
Vapor Presure 0Pa at 25℃
Appearance Yellow-like viscous liquid
Color Clear colorless to slightly yellow
Merck 14,2947
BRN 1724947
pKa 13.03±0.20(Predicted)
PH pH (100g/l,25℃) : 8.5~10.5
Storage Condition 2-8°C
Sensitive Hygroscopic
Refractive Index 1.495-1.502
MDL MFCD00065006
Physical and Chemical Properties Density 1.20
boiling point 118-120°C
refractive index 1.495-1.502
specific optical rotation 30.5 ° (c = 5, H2O on anh. sub)
water soluble
Use Widely used in medicine, food, cosmetics and liquid preparations

Risk and Safety

Hazard Symbols Xn - Harmful
Harmful
Risk Codes R36/37/38 - Irritating to eyes, respiratory system and skin.
R48 - Danger of serious damage to health by prolonged exposure
R41 - Risk of serious damage to eyes
R37/38 - Irritating to respiratory system and skin.
R20/21/22 - Harmful by inhalation, in contact with skin and if swallowed.
Safety Description S23 - Do not breathe vapour.
S24/25 - Avoid contact with skin and eyes.
S45 - In case of accident or if you feel unwell, seek medical advice immediately (show the label whenever possible.)
S36/37/39 - Wear suitable protective clothing, gloves and eye/face protection.
S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S22 - Do not breathe dust.
WGK Germany 1
RTECS ES4316000
FLUKA BRAND F CODES 3-10
TSCA Yes
HS Code 29241990
Toxicity LD50 oral in mouse: 15gm/kg

Introduction

It is more stable in aqueous solution, but prolonged heating causes racemization.

 

LogP -1.06 at 22℃
Introduction D-panthenol (D-panthenol) is an active compound of D-pantothenic acid and a precursor of coenzyme A, it is an important vitamin drug, which can be converted into pantothenic acid and then synthesized into coenzyme A. It promotes the metabolism of human protein, fat and carbohydrate, protects the mucous membrane and luster of skin surface, and prevents the occurrence of diseases, D-panthenol as a nutritional supplement, widely used in medicine, food, cosmetics industry, specific preparations such as Oral Liquid, eye drops, multi-vitamin injection, shampoo, mousse, skin cream, etc.
properties is a colorless to yellowish transparent viscous liquid that may crystallize during long-term low-temperature storage. There is a slight special odor, easy to absorb moisture. D-panthenol soluble in water, methanol, ethanol, insoluble in ether, chloroform, oil and fat. It is relatively stable in air and light.
Application dexpanthenol (D-panthenol) is an active compound of D-pantothenic acid and a precursor of coenzyme A, it is an important vitamin drug, which can be converted into pantothenic acid and then synthesized into coenzyme A. It promotes the metabolism of human protein, fat and carbohydrate, protects the mucous membrane and luster of skin surface, and prevents the occurrence of diseases, D-panthenol as a nutritional supplement, widely used in medicine, food, cosmetics industry, specific preparations such as Oral Liquid, eye drops, multi-vitamin injection, shampoo, mousse, skin cream, etc.
range of use is widely used in the pharmaceutical, food, and cosmetic industries. In the pharmaceutical industry, as a vitamin B drug, involved in metabolism; In the food industry, used as a nutritional supplement and fortifier, promote the metabolism of human protein, fat, carbohydrate, maintain the skin and mucous membranes, improve hair gloss, improve immunity, prevent the occurrence of diseases; In the cosmetics industry: the role of care on the skin is manifested in the deep penetration of moisturizers, stimulate the growth of epithelial cells, promote wound healing, anti-inflammatory effect; The role of care on the hair is manifested in a lasting moisturizing function, prevent split hair, damage, increase the density of the hair, improve the luster of the hair; the nursing of the nail is manifested by improving the hydration of the nail and imparting flexibility to the nail.
identification test in 1 Ml of 10% sample solution, add sodium hydroxide solution (TS-224)5Ml and copper sulfate solution (TS-78) drops, vigorous shaking. Should present dark blue. 1 ml of 1mol/L hydrochloric acid was added to 1 ml of 1% aqueous sample solution, and the mixture was heated on a steam bath for about 30min. After cooling, 100mg of hydroxylamine hydrochloride was added and mixed well, and 5ml of sodium hydroxide solution (TS-224) was added. After standing for 5min, the pH value was adjusted to 2.5-3.0 with 1mol/L hydrochloric acid, and 1 drop of ferric chloride test solution (TS-101) was added. Should appear reddish purple.
content analysis accurately weigh a sample of about 400mg and place it in a reflux flask with a standard port, add 50.0mL 0.1mol/L perchloric acid in glacial acetic acid solution and reflux for 5H. After cooling, the condenser was covered with a metal foil to prevent water contamination, and the condenser was rinsed with glacial acetic acid. Add 5 drops of crystal violet test solution (TSl74), then use 0.1mol/L potassium hydrogen phthalate glacial acetic acid solution titration to Blue Green end point. At the same time, the blank test was carried out and the necessary correction was made. Perchloric acid is equivalent to 20.53mg of panthenol (C9H1 9NO4) per mL of 0.1mol/L.
toxicity GRAS(FDA,§ 182.5580,2000).
Use for hair care, skin moisturizers, and helps skin wound healing, fight inflammation,
It is widely used as pharmaceutical intermediates in medicine, food, cosmetics and liquid preparations
.
is a precursor of vitamin B5.
production method 1. D-pantolactone and 3-aminopropanol were mixed in methanol and condensed. The reaction was as follows:

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