L-Alanine - PharmPure™, USP, ChP, JP, Ph.Eur. , CAS No.56-41-7

CAS: 56-41-7 Cat. No.: GMP1527702 Molecular Weight: 89.09 Beilstein Registry Number: 1720248 EC Number: 200-273-8
AVAILABLE TO ORDER
GRADE & PURITY PharmPure™ ? PharmPure™ — Aladdin's line of biopharmaceutical raw and starting materials. Use for pharma manufacturing inputs needing high purity and documentation. USP ? United States Pharmacopeia grade — meets USP monograph specs for pharmaceutical use. Use for drug manufacturing, QC, and applications requiring US compendial compliance. ChP ? Chinese Pharmacopoeia grade — meets ChP (中国药典) monograph specifications. Use for pharmaceutical work requiring compliance with Chinese standards. JP ? Japanese Pharmacopoeia grade — conforms to JP monograph standards. Use for pharmaceutical products subject to Japanese regulatory requirements. Ph.Eur. ? European Pharmacopoeia grade — conforms to Ph.Eur. monographs across EU member states. Use for pharmaceutical work needing European compendial compliance.
Storage
Room temperature,Desiccated
Shipped In
Normal
 ·  off list, applied to all prices below.
Size
Status
Price
Qty
100g
GMP1527702-100g
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.
$299.90
500g
GMP1527702-500g
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.
$699.90
Enter a quantity for the sizes you want to add.
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Why this grade

PharmPure™, USP, ChP, JP, Ph.Eur. ChP,JP,Ph.Eur.,PharmPure™,USP for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Room temperature,Desiccated Ships Normal Check lot-specific COA for exact specifications.

📋

Quality documents

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

📚

Literature proof

Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Overview

L-Alanine is a nonessential amino acid that plays a key role in the glucose-alanine cycle between muscle tissue and the liver. In amino acid-degrading tissues such as muscle, amino groups are pooled as glutamate by transamination reactions. The amino group of glutamate is transferred to pyruvate via alanine aminotransferase, forming alanine and α-ketoglutarate. The alanine is passed into the blood and transported to the liver. This reaction is reversed in the liver where pyruvate can be used in gluconeogenesis to form glucose, which may return to other tissues through the circulatory system.
A nonessential amino acid that plays a key role in the glucose-alanine cycle

Specifications

Specifications & Purity
PharmPure™, USP, ChP, JP, Ph.Eur.
Storage
Room temperature, Desiccated
Shipped In
Normal
Grade
ChP, JP, Ph.Eur., PharmPure™, USP
Names and Identifiers
Canonical SmilesCC(C(=O)O)N
IUPAC Name(2S)-2-aminopropanoic acid
InChIKeyQNAYBMKLOCPYGJ-REOHCLBHSA-N
INCHI1S/C3H7NO2/c1-2(4)3(5)6/h2H,4H2,1H3,(H,5,6)/t2-/m0/s1
Isomeric SMILES C[C@@H](C(=O)O)N
WGK Germany 1
RTECS AY2990000
Alternate CAS 56-41-7,18875-37-1,25191-17-7,77160-91-9,25191-17-7
MeSH Entry Terms Abuf\u00e8ne;Alanine;Alanine, L Isomer;Alanine, L-Isomer;L Alanine;L-Alanine;L-Isomer Alanine
Molecular Weight 89.09
Beilstein 1720248
Reaxy-Rn 635807
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=635807&ln=

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
SuperclassOrganic acids and derivatives
ClassCarboxylic acids and derivatives
SubclassAmino acids, peptides, and analogues
Intermediate Tree Nodes Amino acids and derivatives - Alpha amino acids and derivatives
Direct ParentAlanine and derivatives
Alternative Parents L-alpha-amino acids  Amino acids  Monocarboxylic acids and derivatives  Carboxylic acids  Organopnictogen compounds  Organic oxides  Monoalkylamines  Hydrocarbon derivatives  Carbonyl compounds  
Molecular FrameworkAliphatic acyclic compounds
Substituents Alanine or derivatives - Alpha-amino acid - L-alpha-amino acid - Amino acid - Carboxylic acid - Monocarboxylic acid or derivatives - Hydrocarbon derivative - Organic oxygen compound - Primary amine - Organooxygen compound - Organonitrogen compound - Organic nitrogen compound - Primary aliphatic amine - Carbonyl group - Amine - Organopnictogen compound - Organic oxide - Aliphatic acyclic compound
DescriptionThis compound belongs to the class of organic compounds known as alanine and derivatives. These are compounds containing alanine or a derivative thereof resulting from reaction of alanine at the amino group or the carboxy group, or from the replacement of any hydrogen of glycine by a heteroatom.
External Descriptors Common amino acids
Certificates(CoA,COO,BSE/TSE and Analysis Chart)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
Chemical and Physical Properties
Specific Rotation[α]14 ° (C=10, HCl)
Melt Point(°C)314-316°C
Molecular Weight89.090 g/mol
XLogP3-3.000
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count3
Rotatable Bond Count1
Exact Mass89.0477 Da
Monoisotopic Mass89.0477 Da
Topological Polar Surface Area63.300 Ų
Heavy Atom Count6
Formal Charge0
Complexity61.800
Isotope Atom Count0
Defined Atom Stereocenter Count1
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Solution Calculators
Reviews

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