Lipase from Pseudomonas fluorescens, CAS No.9001-62-1

CAS: 9001-62-1 Cat. No.: L299014 Número CE: 232-619-9 PubChem CID: 135534490
Disponível para encomenda
GRADE & PURITY EnzymoPure™ ? EnzymoPure™ — Aladdin's line of high-quality enzymatic solutions. Use when enzyme purity and defined activity drive assay or process performance. ≥20,000 U/g
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Size
Alemanha (EU)
USA*
Price
Qty
10g
L299014-10g
—
Em stock ≥10
104,04€
50g
L299014-50g
—
1 Em stock
268,04€
Enter a quantity for the sizes you want to add.
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Why this grade

EnzymoPure™, ≥20,000 U/g EnzymoPure™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Store at 2-8°C Ships Wet ice Check lot-specific COA for exact specifications.

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Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

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Literature proof

Cited in 232 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Visão geral

Product Application:

Lipase from Pseudomonas fluorescens can be used as a biocatalyst in the hydrolysis and transesterification of parabens (para-hydroxybenzoic acid esters),enzymatic kinetic resolution of chlorohydrins,regio-selective acylation of andrographolide with different acylating agents to synthesize andrographolide derivatives. Lipase can also immobilized on silk fibroin spheres to prepare optically active epoxides by enzymatic kinetic resolution of halohydrins.Usually used industrially for the resolution of chiral compounds and the transesterification production of biodiesel.

Specifications

Product Name
Lipase from Pseudomonas fluorescens, CAS No.9001-62-1
Sinónimos
PPL | Lipase AY 30 | NSC87878 | NSC-87878 | FT-0627873 | A854526 | RIZOLIPASE | AKOS032947557 | A854191 | 1, 4-(2-pyridinylazo)-, disodium salt | sodium;4-(pyridin-2-yldiazenyl)benzene-1,3-diol | Lipase, triacylglycerol
Grau
EnzymoPure™
Especificações e pureza
EnzymoPure™, ≥20,000 U/g
Mecanismos bioquímicos e fisiológicos
Lipases catalyze the hydrolysis of esters in aqueous solutions,the hydrolysis of triacylglycerols into glycerol and free fatty acids, and the synthesis of esters in non-aqueous solutions,and also produce hydroxyl and carboxylic groups through the hydrolys
CAS
9001-62-1
Número da Comissão das Enzimas
3.1.1.3.
Tipo de molécula
Enzyme
Armazenamento e envio
Concentração
≥20,000 U/g
Condições de armazenamento de armazenamento
Store at 2-8°C
Enviado em
Wet ice

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassBenzenoids
ClassePhenols
SubclassBenzenediols
Intermediate Tree Nodes Not available
Direct ParentResorcinols
Alternative Parents 1-hydroxy-4-unsubstituted benzenoids  1-hydroxy-2-unsubstituted benzenoids  Pyridines and derivatives  Benzene and substituted derivatives  Heteroaromatic compounds  Azo compounds  Organic alkali metal salts  Azacyclic compounds  Organopnictogen compounds  Organooxygen compounds  Hydrocarbon derivatives  Organic cations  
Molecular FrameworkAromatic heteromonocyclic compounds
Substituents Resorcinol - 1-hydroxy-4-unsubstituted benzenoid - 1-hydroxy-2-unsubstituted benzenoid - Pyridine - Monocyclic benzene moiety - Heteroaromatic compound - Azo compound - Azacycle - Organic alkali metal salt - Organoheterocyclic compound - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Hydrocarbon derivative - Organic salt - Organooxygen compound - Organonitrogen compound - Organic cation - Aromatic heteromonocyclic compound
DescriçãoThis compound belongs to the class of organic compounds known as resorcinols. These are compounds containing a resorcinol moiety, which is a benzene ring bearing two hydroxyl groups at positions 1 and 3.
External Descriptors Not available
Certificados(CoA,COO,BSE/TSE e Mapa de Análise)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

9 results found

Lot NumberCertificate TypeDataItem
L2509486Certificate of AnalysisApr 11, 2025 L299014
L2509487Certificate of AnalysisApr 11, 2025 L299014
G2419543Certificate of AnalysisJul 12, 2024 L299014
G2419544Certificate of AnalysisJul 12, 2024 L299014
G2419571Certificate of AnalysisJul 12, 2024 L299014
F1917216Certificate of AnalysisJan 04, 2023 L299014
A2212069Certificate of AnalysisJan 24, 2022 L299014
B2210113Certificate of AnalysisJan 12, 2022 L299014
B2210163Certificate of AnalysisJan 12, 2022 L299014
FAQs e artigos
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Lipase (Triacylglycerol Hydrolase): Interfacial Catalysis, Selectivity Classes, and Assay/Application Systems
Review of the Principles, Common Methods, and Key Application Considerations for the Determination of Glycerol and Triglyceride Contents
Review of the Structural Characteristics, Biological Functions, and Application Advances of Lycopene
Application of Fatty Acid Methyl Ester Sulfonate (MES) in Household Detergent and Cleaning Formulations: Detergency, Hard-Water Tolerance, and Selection Criteria
Performance Sources and Formulation Applications of Enzyme-Based Ingredients in Daily Chemical Products: Fermentation Transformation, Enzymatic Reactions, and Application Principles
Structure, Degradation Behavior, and Applications of Poly(trimethylene carbonate) (PTMC) in Flexible Absorbable Materials
Citations of This Product
Calculadoras de soluções
Revisões

Avaliações dos Clientes

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