Welcome to LookChem.com Sign In|Join Free

CAS

  • or
5-N-HEPTADECYLRESORCINOL, also known as 5-Heptadecylresorcinol, is a member of the alk(en)ylresorcinols (ARs) group. It is characterized by its pharmacological properties, which include anti-inflammatory, anti-carcinogenic, and anti-microbial bioactivities. 5-N-HEPTADECYLRESORCINOL is predominantly found in various cereals and plant sources such as barley, spelt, wheat, rye, ginkgo, mango peels, pulp, and peas.

41442-57-3 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • 41442-57-3 Structure
  • Basic information

    1. Product Name: 5-N-HEPTADECYLRESORCINOL
    2. Synonyms: 5-N-HEPTADECYLRESORCINOL;5-Heptadecylbenzene-1,3-diol;5-Heptadecyl-1,3-benzenediol;5-Heptadecyl-1,3-dihydroxybenzene
    3. CAS NO:41442-57-3
    4. Molecular Formula: C23H40O2
    5. Molecular Weight: 348.5625
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 41442-57-3.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 478°Cat760mmHg
    3. Flash Point: 202.6°C
    4. Appearance: /
    5. Density: 0.95g/cm3
    6. Vapor Pressure: 9.24E-10mmHg at 25°C
    7. Refractive Index: 1.506
    8. Storage Temp.: 2-8°C
    9. Solubility: N/A
    10. BRN: 2287460
    11. CAS DataBase Reference: 5-N-HEPTADECYLRESORCINOL(CAS DataBase Reference)
    12. NIST Chemistry Reference: 5-N-HEPTADECYLRESORCINOL(41442-57-3)
    13. EPA Substance Registry System: 5-N-HEPTADECYLRESORCINOL(41442-57-3)
  • Safety Data

    1. Hazard Codes: Xi
    2. Statements: 36
    3. Safety Statements: 26
    4. WGK Germany: 3
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 41442-57-3(Hazardous Substances Data)

41442-57-3 Usage

Uses

Used in Analytical Chemistry:
5-N-HEPTADECYLRESORCINOL is used as an analytical reference standard for the quantification of the analyte in agricultural products. It aids in the accurate measurement of the compound in mango peels, rye grains, and other cereals using different chromatography techniques.
Used in Pharmaceutical Applications:
Given its anti-inflammatory, anti-carcinogenic, and anti-microbial properties, 5-N-HEPTADECYLRESORCINOL holds potential for development as a pharmaceutical agent. It can be utilized in the creation of drugs targeting inflammation, cancer, and microbial infections.
Used in the Food Industry:
5-N-HEPTADECYLRESORCINOL can be employed in the food industry to enhance the nutritional and health-promoting properties of cereal-based products. Its presence in various cereals and plant sources makes it a valuable additive for improving the overall quality and health benefits of the final product.
Used in Cosmetics:
Due to its anti-inflammatory and anti-microbial properties, 5-N-HEPTADECYLRESORCINOL may also find applications in the cosmetics industry. It could be used in the development of skincare products aimed at reducing inflammation and combating microbial infections on the skin.

Check Digit Verification of cas no

The CAS Registry Mumber 41442-57-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,4,4 and 2 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 41442-57:
(7*4)+(6*1)+(5*4)+(4*4)+(3*2)+(2*5)+(1*7)=93
93 % 10 = 3
So 41442-57-3 is a valid CAS Registry Number.
InChI:InChI=1/C23H40O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-21-18-22(24)20-23(25)19-21/h18-20,24-25H,2-17H2,1H3

41442-57-3 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • Sigma-Aldrich

  • (97001)  5-Heptadecylresorcinol  analytical standard

  • 41442-57-3

  • 97001-10MG

  • 6,686.55CNY

  • Detail

41442-57-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-heptadecylbenzene-1,3-diol

1.2 Other means of identification

Product number -
Other names 5-Heptadecyl-1,3-dihydroxybenzene

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:41442-57-3 SDS

41442-57-3Relevant articles and documents

Synthesis and inhibitory activities against colon cancer cell growth and proteasome of alkylresorcinols

Zhu, Yingdong,Soroka, Dominique N.,Sang, Shengmin

, p. 8624 - 8631 (2012/11/13)

We have identified alkylresorcinols (ARs) as the major active components in wheat bran against human colon cancer cell growth (HCT-116 and HT-29) using a bioassay-guided approach. To further study the structure-activity relationships, 15 ARs and their intermediates (1-15) were synthesized expediently by the modified Wittig reaction in aqueous media, and six 5-alkylpyrogallols and their analogues (16-21) were prepared by the general Grignard reaction. The synthetic AR analogues were evaluated for activities against the growth of human colon cancer cells HCT-116 and HT-29 and the chymotrypsin-like activity of the human 20S proteasome. Our results found that (1) AR C13:0 and C15:0 (13 and 14) had the greatest inhibitory effects in human colon cancer cells HCT-116 and HT-29, while decreasing or increasing the side chain lengths diminished the activities; (2) two free meta-hydroxyl groups at C-1 and C-3 on the aromatic ring of the AR analogues greatly contributed to their antitumor activity; (3) the introduction of a third hydroxyl group at C-2 (20 and 21) into the aromatic ring of the AR analogues yielded no significant enhancement in activity against HCT-116 cells and decimated the effects against HT-29 cells, but dramatically increased the activity against the chymotrypsin-like activity of the human 20S proteasome; and (4) AR C11:0 (12) was found to have the greatest effect in a series of AR C9:0-C17:0 against the chymotrypsin-like activity of the human 20S proteasome.

Alkylresorcylic acid synthesis by type III polyketide synthases from rice Oryza sativa

Matsuzawa, Miku,Katsuyama, Yohei,Funa, Nobutaka,Horinouchi, Sueharu

experimental part, p. 1059 - 1067 (2011/03/20)

Alkylresorcinols, produced by various plants, bacteria, and fungi, are bioactive compounds possessing beneficial activities for human health, such as anti-cancer activity. In rice, they accumulate in seedlings, contributing to protection against fungi. Alkylresorcylic acids, which are carboxylated forms of alkylresorcinols, are unstable compounds and decarboxylate readily to yield alkylresorcinols. Genome mining of the rice Oryza sativa identified two type III polyketide synthases, named ARAS1 (alkylresorcylic acid synthase) and ARAS2, that catalyze the formation of alkylresorcylic acids. Both enzymes condensed fatty acyl-CoAs with three C2 units from malonyl-CoA and cyclized the resulting tetraketide intermediates via intramolecular C-2 to C-7 aldol condensation. The alkylresorcylic acids thus produced were released from the enzyme and decarboxylated non-enzymatically to yield alkylresorcinols. This is the first report on a plant type III polyketide synthase that produces tetraketide alkylresorcylic acids as major products.

An expedient synthesis of 5-n-alkylresorcinols and novel 5-n-alkylresorcinol haptens

Parikka, Kirsti,Waehaelae, Kristiina

supporting information; experimental part, (2010/04/22)

The first synthesis of bioactive long alkyl chain 5-n-alkylresorcinols, present in whole grain products, by a novel modification of the Wittig reaction is described. All the main long chain 5-n-alkylresorcinols present in rye and wheat, including C23 and C25 analogues and haptens, which have not been previously prepared, were synthesised. Microwave-promoted reactions of a semistabilized ylid and alkanals in water gave good yields in both pressurized and open systems. An alternative microwave-promoted synthesis starting from non-stabilized alkyltriphenylphosphonium salts and 3,5-dimethoxybenzaldehyde worked as well. Aqueous media were suitable for the reactions even if the starting materials were not soluble in water. The 5-n-alkylresorcinols are potential biomarkers of whole grain intake, and the new hapten derivatives of 5-n-alkylresorcinols will open the way for the immunochemical detection techniques of alkylresorcinols.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 41442-57-3