Glycine - PharmPure™, USP, ChP, JP, BP, Ph.Eur. , CAS No.56-40-6

CAS: 56-40-6 Cat. No.: GMP1527736 Molecular Weight: 75.07 Beilstein Registry Number: 635782 EC Number: 200-272-2
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. BP ? British Pharmacopoeia grade — conforms to BP monograph requirements. Use for pharmaceutical products marketed under UK/BP regulatory standards. 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
Shipped In
Normal
 ·  off list, applied to all prices below.
Size
Status
Price
Qty
250g
GMP1527736-250g
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.
$529.90
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Why this grade

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

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Storage & shipping

Room temperature 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.

Specifications

Specifications & Purity
PharmPure™, USP, ChP, JP, BP, Ph.Eur.
Biochemical and Physiological Mechanisms
Glycine is a non essential amino acid. Calcium influx through the cell membrane is mediated by glycine gated channels. Glycine participates in the synthesis of porphyrins, purines, and serines. It can also serve as a competitive agonist for binding glutam
Storage
Room temperature
Shipped In
Normal
Grade
BP, ChP, JP, Ph.Eur., PharmPure™, USP
Names and Identifiers
Canonical SmilesC(C(=O)O)N
IUPAC Name2-aminoacetic acid
InChIKeyDHMQDGOQFOQNFH-UHFFFAOYSA-N
INCHI1S/C2H5NO2/c3-1-2(4)5/h1,3H2,(H,4,5)
Isomeric SMILES C(C(=O)O)N
WGK Germany 1
RTECS MB7600000
Molecular Weight 75.07
Beilstein 635782
Reaxy-Rn 635782
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=635782&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 ParentAlpha amino acids
Alternative Parents Amino acids  Monocarboxylic acids and derivatives  Carboxylic acids  Organopnictogen compounds  Organic oxides  Monoalkylamines  Hydrocarbon derivatives  Carbonyl compounds  
Molecular FrameworkAliphatic acyclic compounds
Substituents Alpha-amino acid - Amino acid - Carboxylic acid - Monocarboxylic acid or derivatives - Organic nitrogen compound - Organic oxide - Hydrocarbon derivative - Primary amine - Organooxygen compound - Organonitrogen compound - Organopnictogen compound - Primary aliphatic amine - Organic oxygen compound - Carbonyl group - Amine - Aliphatic acyclic compound
DescriptionThis compound belongs to the class of organic compounds known as alpha amino acids. These are amino acids in which the amino group is attached to the carbon atom immediately adjacent to the carboxylate group (alpha carbon).
External Descriptors Common amino acids - Amino acids
Certificates(CoA,COO,BSE/TSE and Analysis Chart)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
Chemical and Physical Properties
SolubilityEasy to dissolve in water, solubility in water: 25g/100ml at 25 ℃; 39.1g/100ml at 50 ℃; 54.4g/100ml at 75 ℃; At 100 ℃, it is 67.2g/100ml. Extremely insoluble in ethanol, approximately 0.06g dissolved in 100g of anhydrous ethanol. Almost insoluble in aceto
Melt Point(°C)240 °C
Molecular Weight75.070 g/mol
XLogP3-3.200
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count3
Rotatable Bond Count1
Exact Mass75.032 Da
Monoisotopic Mass75.032 Da
Topological Polar Surface Area63.300 Ų
Heavy Atom Count5
Formal Charge0
Complexity42.900
Isotope Atom Count0
Defined Atom Stereocenter Count0
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
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