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1-Heptacosanol is a long-chain primary aliphatic alcohol characterized by a heptacosyl group attached to a hydroxyl group. It is a naturally occurring wax alcohol found in various plant waxes, such as those from sugar cane and wheat germ. This versatile chemical is known for its emollient and emulsifying properties, as well as its potential therapeutic effects, making it a valuable component in a variety of industries.

2004-39-9

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2004-39-9 Usage

Uses

Used in Cosmetics and Personal Care Products:
1-Heptacosanol is used as an emollient and emulsifier for its ability to soften and smooth the skin, as well as to stabilize formulations and improve the texture of products.
Used in Pharmaceuticals:
1-Heptacosanol is used as an excipient in pharmaceutical formulations to enhance the solubility and stability of active ingredients, as well as to improve the overall quality of the final product.
Used in Industrial Applications:
1-Heptacosanol is used as a component in various industrial products, such as lubricants, coatings, and plastics, due to its unique chemical properties and compatibility with other materials.
Used in Cholesterol Management:
1-Heptacosanol is used as a dietary supplement for its potential cholesterol-lowering effects, which may contribute to improved cardiovascular health.
Used in Antioxidant Formulations:
1-Heptacosanol is used as an antioxidant to protect against lipid peroxidation, which can help maintain the integrity of cell membranes and prevent oxidative damage.
Used in Anti-Inflammatory Applications:
1-Heptacosanol is used as an anti-inflammatory agent for its potential to reduce inflammation and support the body's natural healing processes.
Used in Neuroprotective Therapies:
1-Heptacosanol is used in research for its potential neuroprotective properties, which may help protect neurons from damage and support brain health.

Check Digit Verification of cas no

The CAS Registry Mumber 2004-39-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,0,0 and 4 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 2004-39:
(6*2)+(5*0)+(4*0)+(3*4)+(2*3)+(1*9)=39
39 % 10 = 9
So 2004-39-9 is a valid CAS Registry Number.
InChI:InChI=1/C27H56O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22-23-24-25-26-27-28/h28H,2-27H2,1H3

2004-39-9 Well-known Company Product Price

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  • (Code)Product description
  • CAS number
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  • Sigma

  • (H6764)  1-Heptacosanol  ≥98%

  • 2004-39-9

  • H6764-100MG

  • 1,536.21CNY

  • Detail
  • Sigma

  • (H6764)  1-Heptacosanol  ≥98%

  • 2004-39-9

  • H6764-250MG

  • 3,747.51CNY

  • Detail

2004-39-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-Heptacosanol

1.2 Other means of identification

Product number -
Other names heptacosan-1-ol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:2004-39-9 SDS

2004-39-9Downstream Products

2004-39-9Relevant academic research and scientific papers

Branched Long Chain Alkyl Methyl Ethers: A New Class of Lipids from Spider Silk

Schulz, Stefan,Toft, Soeren

, p. 6805 - 6820 (2007/10/02)

Long chain methyl branched 1-methoxyalkanes, a new class of ether lipids, have been identified from silk of the spider Linyphia triangularis (Araneae: Linyphiidae) by use of gas chromatographic retention indices, GC/MS investigations, and chemical modifications.Methyl groups are predominantly located at C-2, and ω-3 or ω-2 positions, respectively.Chain length varies between C24 and C32.The synthesis of representative compounds is reported.

A New Synthesis of Long Chain Acid Esters and Carbinols

Rao, S. Jagadishwar,Bhalerao, U. T.,Tilak, B. D.

, p. 208 - 211 (2007/10/02)

A versatile synthesis of difficulty accessible long chain acid esters and carbinols is described.The synthesis involves acylations at 2- and 5-positions of thiophene.Thioketalation of the resulting ketoesters followed by Raney nickel desulfurization yield acid esters which on LAH reduction give the corresponding carbinols.

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