Cystathionine - ≥90%(HPLC) , CAS No.535-34-2

CAS: 535-34-2 Cat. No.: D136654 Formule: HOOCCH(NH2)CH2CH2SCH2CH(NH2)COOH Poids moléculaire: 222.26 Numéro CE: 208-613-7
DISPONIBLE À COMMANDE
GRADE & PURITY ≥90%(HPLC)
Synonyms
EN300-246200 | DL-Cystathionine | (2-Amino-2-carboxyethyl)homocysteine # | FT-0665422 | ORTHO-N-VALERICACIDTRIETHYLESTER | 2-amino-4-[(2-amino-2-carboxyethyl)sulfanyl]butanoic acid | FT-0627595 | NSC 118379 | ILRYLPWNYFXEMH-UHFFFAOYSA-N | S-(2-Amino-2-car
Storage
Store at 2-8°C
Shipped In
Wet ice
★
Size
Allemagne (EU)
USA*
Price
Qty
25mg
D136654-25mg
—
2 En stock
676,75€
Enter a quantity for the sizes you want to add.
🧪
Why this grade

≥90%(HPLC) for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Store at 2-8°C Ships Wet ice 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 2 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Vue d’ensemble

Cystathionine is an intermediate in the biosynthesis of the amino acid cysteine.
Cystathionine is used as a substrate to differentiate and analyze cystathionine gamma-lyase(s).

Specifications

Synonymes
EN300-246200 | DL-Cystathionine | (2-Amino-2-carboxyethyl)homocysteine # | FT-0665422 | ORTHO-N-VALERICACIDTRIETHYLESTER | 2-amino-4-[(2-amino-2-carboxyethyl)sulfanyl]butanoic acid | FT-0627595 | NSC 118379 | ILRYLPWNYFXEMH-UHFFFAOYSA-N | S-(2-Amino-2-car
Spécifications et pureté
≥90%(HPLC)
Mécanismes biochimiques et physiologiques
胱硫醚是氨基酸半胱氨酸生物合成的一种中间体。胱硫醚可作为底物用于区分和分析胱硫醚γ-裂合酶。
Conditions de stockage de stockage
Store at 2-8°C
Expédié en
Wet ice
Ce produit nécessite l'expédition en chaîne froide. Les services terrestres et autres services économiques ne sont pas disponibles.
Pureté
≥90%(HPLC)
Noms et identifiants
Sourires canoniques
C(CSCC(C(=O)O)N)C(C(=O)O)N
IUPAC Name
2-amino-4-(2-amino-2-carboxyethyl)sulfanylbutanoic acid
InChIKey
ILRYLPWNYFXEMH-UHFFFAOYSA-N
INCHI
1S/C7H14N2O4S/c8-4(6(10)11)1-2-14-3-5(9)7(12)13/h4-5H,1-3,8-9H2,(H,10,11)(H,12,13)
Isomères SMILES
C(CSCC(C(=O)O)N)C(C(=O)O)N
Poids moléculaire
222.26

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
ClasseCarboxylic acids and derivatives
SubclassAmino acids, peptides, and analogues
Intermediate Tree Nodes Amino acids and derivatives - Alpha amino acids and derivatives
Direct ParentCysteine and derivatives
Alternative Parents Alpha amino acids  Thia fatty acids  Dicarboxylic acids and derivatives  Amino acids  Sulfenyl compounds  Dialkylthioethers  Carboxylic acids  Organopnictogen compounds  Organic oxides  Monoalkylamines  Hydrocarbon derivatives  Carbonyl compounds  
Molecular FrameworkAliphatic acyclic compounds
Substituents Cysteine or derivatives - Alpha-amino acid - Thia fatty acid - Dicarboxylic acid or derivatives - Fatty acid - Fatty acyl - Amino acid - Carboxylic acid - Thioether - Sulfenyl compound - Dialkylthioether - Organic nitrogen compound - Organopnictogen compound - Primary amine - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Primary aliphatic amine - Organic oxygen compound - Amine - Carbonyl group - Organic oxide - Hydrocarbon derivative - Aliphatic acyclic compound
DescriptionThis compound belongs to the class of organic compounds known as cysteine and derivatives. These are compounds containing cysteine or a derivative thereof resulting from reaction of cysteine at the amino group or the carboxy group, or from the replacement of any hydrogen of glycine by a heteroatom.
External Descriptors cystathionines
Structure 3D
Modèle de structure chimique interactif





Mécanismes d'action
Certificats (CoA, COO, BSE/TSE et tableau d'analyse)
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.

7 results found

Lot NumberCertificate TypeDateArticle
K2118376Certificate of AnalysisSep 15, 2023 D136654
K2118377Certificate of AnalysisSep 15, 2023 D136654
C2127295Certificate of AnalysisJan 12, 2023 D136654
C2127298Certificate of AnalysisJan 12, 2023 D136654
B2317649Certificate of AnalysisJan 06, 2023 D136654
B2317694Certificate of AnalysisJan 06, 2023 D136654
B2317706Certificate of AnalysisJan 06, 2023 D136654
Propriétés chimiques et physiques
SolubilitéMiscible with water., Miscible with water.
Point de fusion (°C)281 °C
Poids moléculaire222.260 g/mol
XLogP3-6.000
Hydrogen Bond Donor Count4
Hydrogen Bond Acceptor Count7
Rotatable Bond Count7
Exact Mass222.067 Da
Monoisotopic Mass222.067 Da
Topological Polar Surface Area152.000 Ų
Heavy Atom Count14
Formal Charge0
Complexity212.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count2
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Citations of This Product
Calculateurs de solution
Avis

Avis des clients

Souhaitez-vous que nous vous envoyions un message lorsque des réductions seront disponibles?

Me rappeler plus tard

Merci ! Veuillez vérifier votre boîte de réception e-mail pour confirmer.

Oups ! Les notifications sont désactivées.