Welcome to LookChem.com Sign In|Join Free

CAS

  • or

2507-55-3

Post Buying Request

2507-55-3 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

2507-55-3 Usage

Chemical Properties

Off-White Solid

Uses

Different sources of media describe the Uses of 2507-55-3 differently. You can refer to the following data:
1. As a biological fatty Acid, 2-HydroxyMyristic Acid can be used in cosmetics, skin treatments, and hair preparations.
2. A biological fatty Acid, used in cosmetics, skin treatments, and hair preparations.

Definition

ChEBI: A long-chain fatty acid that is a derivative of myristic acid having a hydroxy substituent at C-2.

Purification Methods

Crystallise the acid from chloroform or twice from MeOH (m 85.8-86.6o) [Horn & Pretorious J Chem Soc 1463 1954, Chibnall et al. Biochem J 30 1034 1963, Beilstein 3 H 361, 3 I 130, 3 II 246

Check Digit Verification of cas no

The CAS Registry Mumber 2507-55-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,0 and 7 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2507-55:
(6*2)+(5*5)+(4*0)+(3*7)+(2*5)+(1*5)=73
73 % 10 = 3
So 2507-55-3 is a valid CAS Registry Number.
InChI:InChI=1/C14H28O3/c1-2-3-4-5-6-7-8-9-10-11-12-13(15)14(16)17/h13,15H,2-12H2,1H3,(H,16,17)/t13-/m0/s1

2507-55-3 Well-known Company Product Price

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

  • (H6771)  2-Hydroxytetradecanoic acid  ≥98% (capillary GC)

  • 2507-55-3

  • H6771-10MG

  • 1,170.00CNY

  • Detail
  • Sigma

  • (H6771)  2-Hydroxytetradecanoic acid  ≥98% (capillary GC)

  • 2507-55-3

  • H6771-25MG

  • 2,384.46CNY

  • Detail
  • Sigma

  • (H6771)  2-Hydroxytetradecanoic acid  ≥98% (capillary GC)

  • 2507-55-3

  • H6771-100MG

  • 7,330.05CNY

  • Detail

2507-55-3SDS

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 2-hydroxymyristic acid

1.2 Other means of identification

Product number -
Other names Tetradecanoic acid, 2-hydroxy-

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:2507-55-3 SDS

2507-55-3Relevant articles and documents

P450Jα: A New, Robust and α-Selective Fatty Acid Hydroxylase Displaying Unexpected 1-Alkene Formation

Armbruster, Julia,Steinmassl, Mathilde,Müller Bogotá, Christina A.,Berg, Gabriele,Nidetzky, Bernd,Dennig, Alexander

, p. 15910 - 15921 (2020/10/29)

Oxyfunctionalization of fatty acids (FAs) is a key step in the design of novel synthetic pathways for biobased/biodegradable polymers, surfactants and fuels. Here, we show the isolation and characterization of a robust FA α-hydroxylase (P450Jα) which catalyses the selective conversion of a broad range of FAs (C6:0-C16:0) and oleic acid (C18:1) with H2O2 as oxidant. Under optimized reaction conditions P450Jα yields α-hydroxy acids all with >95 % regioselectivity, high specific activity (up to 15.2 U mg?1) and efficient coupling of oxidant to product (up to 85 %). Lauric acid (C12:0) turned out to be an excellent substrate with respect to productivity (TON=394 min?1). On preparative scale, conversion of C12:0 reached 83 % (0.9 g L?1) when supplementing H2O2 in fed-batch mode. Under similar conditions P450Jα allowed further the first biocatalytic α-hydroxylation of oleic acid (88 % conversion on 100 mL scale) at high selectivity and in good yields (1.1 g L?1; 79 % isolated yield). Unexpectedly, P450Jα displayed also 1-alkene formation from shorter chain FAs (≤C10:0) showing that oxidative decarboxylation is more widely distributed across this enzyme family than reported previously.

Preparative Asymmetric Synthesis of Canonical and Non-canonical a-amino Acids through Formal Enantioselective Biocatalytic Amination of Carboxylic Acids

Dennig, Alexander,Blaschke, Fabio,Gandomkar, Somayyeh,Tassano, Erika,Nidetzky, Bernd

supporting information, p. 1348 - 1358 (2019/10/28)

Chemical and biocatalytic synthesis of non-canonical a-amino acids (ncAAs) from renewable feedstocks and using mild reaction conditions has not efficiently been solved. Here, we show the development of a three-step, scalable and modular one-pot biocascade for linear conversion of renewable fatty acids (FAs) into enantiopure l-a-amino acids. In module 1, selective a-hydroxylation of FAs is catalyzed by the P450 peroxygenase P450CLA. By using an automated H2O2 supplementation system, efficient conversion (46 to >99%; TTN>3300) of a broad range of FAs (C6:0 to C16:0) into valuable a-hydroxy acids (a-HAs; >90% a-selective) is shown on preparative scale (up to 2.3 gL1 isolated product). In module 2, a redox-neutral hydrogen borrowing cascade (alcohol dehydrogenase/amino acid dehydrogenase) allowed further conversion of a-HAs into l-a-AAs (20 to 99%). Enantiopure l-a-AAs (e.e. >99%) including the pharma synthon l-homo-phenylalanine can be obtained at product titers of up to 2.5 gL1. Based on renewables and excellent atom economy, this biocascade is among the shortest and greenest synthetic routes to structurally diverse and industrially relevant ncAAs.

In situ formation of H2O2 for P450 peroxygenases

Paul, Caroline E.,Churakova, Ekaterina,Maurits, Elmer,Girhard, Marco,Urlacher, Vlada B.,Hollmann, Frank

, p. 5692 - 5696 (2015/01/09)

An in situ H2O2 generation approach to promote P450 peroxygenases catalysis was developed through the use of the nicotinamide cofactor analogue 1-benzyl-1,4-dihydronicotinamide (BNAH) and flavin mononucleotide (FMN). Final productivity could be enhanced due to higher enzyme stability at low H2O2 concentrations. The H2O2 generation represented the rate-limiting step, however it could be easily controlled by varying both FMN and BNAH concentrations. Further characterization can result in an optimized ratio of FMN/BNAH/O2/biocatalyst enabling high reaction rates while minimizing H2O2-related inactivation of the enzyme.

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 2507-55-3