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2-Decyldodecanoic Acid, also known as 2-DDA, is a long-chain fatty acid with a unique structure featuring a decyl side chain attached to a dodecanoic acid backbone. It is a synthetic compound with specific chemical properties that make it suitable for various applications in different industries.

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  • 2874-72-8 Structure
  • Basic information

    1. Product Name: 2-DECYLDODECANOIC ACID
    2. Synonyms: 2-DECYLDODECANOIC ACID;Dodecanoic acid,2-decyl-
    3. CAS NO:2874-72-8
    4. Molecular Formula: C22H44O2
    5. Molecular Weight: 340.58
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 2874-72-8.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2-DECYLDODECANOIC ACID(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-DECYLDODECANOIC ACID(2874-72-8)
    11. EPA Substance Registry System: 2-DECYLDODECANOIC ACID(2874-72-8)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 2874-72-8(Hazardous Substances Data)

2874-72-8 Usage

Uses

Used in Pharmaceutical Industry:
2-Decyldodecanoic Acid is used as a reactant for the synthesis of Vizantin, a compound developed as a safe immunostimulant. It plays a crucial role in enhancing the immune response and has potential applications in the treatment of various diseases and conditions.
Used in Chemical Synthesis:
2-Decyldodecanoic Acid can be utilized as a building block in the synthesis of various complex organic compounds, such as surfactants, lubricants, and additives. Its unique structure and properties make it a valuable component in the development of new materials with specific characteristics and functions.

Check Digit Verification of cas no

The CAS Registry Mumber 2874-72-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,8,7 and 4 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 2874-72:
(6*2)+(5*8)+(4*7)+(3*4)+(2*7)+(1*2)=108
108 % 10 = 8
So 2874-72-8 is a valid CAS Registry Number.

2874-72-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-DECYLDODECANOIC ACID

1.2 Other means of identification

Product number -
Other names 2-Decyl-dodecansaeure

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:2874-72-8 SDS

2874-72-8Relevant articles and documents

Development of vizantin, a safe immunostimulant, based on the structure-activity relationship of trehalose-6,6′-dicorynomycolate

Yamamoto, Hirofumi,Oda, Masataka,Nakano, Mayo,Watanabe, Naoyuki,Yabiku, Kenta,Shibutani, Masahiro,Inoue, Masahisa,Imagawa, Hiroshi,Nagahama, Masahiro,Himeno, Seiichiro,Setsu, Kojun,Sakurai, Jun,Nishizawa, Mugio

supporting information, p. 381 - 385 (2013/02/23)

Vizantin, 6,6′-bis-O-(3-nonyldodecanoyl)-α,α′- trehalose, was developed as a safe immunostimulator on the basis of a structure-activity relationship (SAR) study with trehalose 6,6′- dicorynomycolate (TDCM). It was possible to synthesize vizantin on a large scale more easily than in the case of TDCM, and the compound exhibited more potent prophylactic effect on experimental lung metastasis of B16-F0 melanoma cells. Because vizantin stimulated human macrophages, it is a promising candidate for clinical application.

TREHALOSE COMPOUND, METHOD FOR PRODUCING SAME, AND PHARMACEUTICAL PRODUCT CONTAINING THE COMPOUND

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Page/Page column 51; 52, (2011/08/08)

It is an object of the present invention to provide a trehalose compound having high immunopotentiating activity and low toxicity. The trehalose compound is represented by formula (1). (In the formula, X and X' each represents a phenyl, a naphtyl, R1-CHR1- (wherein R1 and R2 each represents a C7-C21 alkyl group or the like) or the like; and n and n' each independently represents an integer of 0-3). The compound exhibits a high activating effect on macrophages and neutrophils.

TREHALOSE COMPOUND, PROCESS FOR PRODUCTION OF THE COMPOUND, AND IMMUNO-STIMULATIVE AGENT COMPRISING THE COMPOUND

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Page/Page column 14-15, (2009/12/07)

An object of the present invention is to provide a novel trehalose compound that exhibits excellent immunostimulating activity and that can be supplied in a large quantity in an industrial scale, and a method for producing the trehalose compound, wherein

Use of branched chain fatty acids and derivatives thereof for inhibition of P-glycoprotein

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, (2008/06/13)

The invention relates to the use of branched chain fatty acids (BFAs) and their derivatives for inhibition of the activity of P-glycoprotein (P-gp). In particular, the invention relates to the use of BFAs and their derivatives in the treatment of multi-drug resistant (MDR) tumors associated with increased activity of P-glycoprotein. The invention also relates to the use of the above-mentioned molecules for administration of biologically active molecules and diagnostic agents into cells associated with increased activity of P-gp, and for increasing accumulation of biologically active molecules and diagnostic agents in organs protected by biological barriers.

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