lipase PS-IM, CAS No.9001-62-1

CAS: 9001-62-1 Cat. No.: L299015 EC Number: 232-619-9 PubChem CID: 135534490
AVAILABLE TO ORDER
GRADE & PURITY EnzymoPure™ ? EnzymoPure™ — Aladdin's line of high-quality enzymatic solutions. Use when enzyme purity and defined activity drive assay or process performance. ≥500 U/g,immobilized on diatomaceous earth
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Size
USA
Germany (EU)*
Price
Qty
10g
L299015-10g
2 In stock
—
$123.90
50g
L299015-50g
2 In stock
—
$366.90
250g
L299015-250g
1 In stock
—
$1,599.90
Enter a quantity for the sizes you want to add.
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Why this grade

EnzymoPure™, ≥500 U/g,immobilized on diatomaceous earth EnzymoPure™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Store at 2-8°C,Argon charged 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 234 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Product Name
lipase PS-IM, CAS No.9001-62-1
Synonyms
9001-62-1 | RIZOLIPASE | Lipase AY 30 | sodium;4-(pyridin-2-yldiazenyl)benzene-1,3-diol | Lipase, triacylglycerol | NSC87878 | NSC-87878 | AKOS032947557 | 1, 4-(2-pyridinylazo)-, disodium salt | FT-0627873 | A854191 | A854526
Grade
EnzymoPure™
Specifications & Purity
EnzymoPure™, ≥500 U/g,immobilized on diatomaceous earth
Biochemical and Physiological Mechanisms
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
Enzyme Commission Number
3.1.1.3
Molecule Type
Enzyme
Storage and Shipping
Concentration
≥500 U/g,immobilized on diatomaceous earth
Storage
Store at 2-8°C,Argon charged
Shipped In
Wet ice
Unit definition
one unit produces 1.0 μmole of (R)-1-phenethyl acetate from 1-phenylethanol per 1 minute at 25℃ in the presence of vinyl acetate.

Documentation

📋 Safety Data Sheet (SDS)

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

<<<<<<< HEAD Download SDS → ======= Download SDS → >>>>>>> release248-p3

✅ 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
ClassPhenols
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
DescriptionThis 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
Certificates (CoA,COO,BSE/TSE and Analysis Chart)
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 TypeDateItem
H2202227H2202227Certificate of AnalysisJan 19, 2026 L299015
H2202228H2202228Certificate of AnalysisJan 19, 2026 L299015
H2202229H2202229Certificate of AnalysisJan 19, 2026 L299015
I2522602I2522602Certificate of AnalysisSep 24, 2025 L299015
A2213625A2213625Certificate of AnalysisJun 09, 2025 L299015
A2213636A2213636Certificate of AnalysisJun 09, 2025 L299015
A2213639A2213639Certificate of AnalysisJun 09, 2025 L299015
I2128219I2128219Certificate of AnalysisApr 03, 2025 L299015
E2423116E2423116Certificate of AnalysisOct 16, 2023 L299015
Documents & Articles
Key Roles of Purified Proteins in the Cleaning Industry and Green Ecology
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
Industrial Biocatalysis Reshaping Manufacturing: Application Systems and Technological Evolution in Industrial Enzymology
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
Solution Calculators
Reviews

Customer Reviews

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