DL-tert-Leucine - ≥98% , CAS No.33105-81-6

CAS: 33105-81-6 Cat. No.: L102895 Peso molecular: 131.17 Beilstein Registry Number: 1721823 Número EC: 608-831-6
Disponible para pedir
GRADE & PURITY ≥98%
Synonyms
AKOS016052444 | DL-Terleucine | psi-Leucine | J-300340 | tert-butylglycine | EN300-73664 | (+/-)-2-Amino-3,3-dimethylbutyric acid, DL-alpha-tert-Butylglycine | AC-24097 | FT-0625515 | AKOS000263225 | Q27140135 | MFCD00004265 | CHEBI:72770 | MFCD00064218 |
Storage
Store at 2-8°C
Shipped In
Wet ice
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
1g
L102895-1g
1

9,90US$

14,90US$
Guardar 5,00 US$ (33.56%)
5g
L102895-5g
3

13,90US$

20,90US$
Guardar 7,00 US$ (33.49%)
25g
L102895-25g
3

56,90US$

85,90US$
Guardar 29,00 US$ (33.76%)
100g
L102895-100g
1

179,90US$

269,90US$
Guardar 90,00 US$ (33.35%)
Enter a quantity for the sizes you want to add.
🧪

Why this grade

≥98% 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 1 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Sinónimos
AKOS016052444 | DL-Terleucine | psi-Leucine | J-300340 | tert-butylglycine | EN300-73664 | (+/-)-2-Amino-3, 3-dimethylbutyric acid, DL-alpha-tert-Butylglycine | AC-24097 | FT-0625515 | AKOS000263225 | Q27140135 | MFCD00004265 | CHEBI:72770 | MFCD00064218 |
Especificaciones y pureza
≥98%
Condiciones de almacenamiento de almacenamiento
Store at 2-8°C
Enviado en
Wet ice
Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.
Pureza
≥98%
Nombres e identificadores
Pubchem Sid504758414
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504758414
Sonrisas canónicasCC(C)(C)C(C(=O)O)N
IUPAC Name2-amino-3,3-dimethylbutanoic acid
InChIKeyNPDBDJFLKKQMCM-UHFFFAOYSA-N
INCHI1S/C6H13NO2/c1-6(2,3)4(7)5(8)9/h4H,7H2,1-3H3,(H,8,9)
Isómeros SMILES CC(C)(C)C(C(=O)O)N
WGK Alemania 3
Peso molecular 131.17
Beilstein 1721823
Reaxy-Rn 1721823
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1721823&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
ClaseCarboxylic acids and derivatives
SubclassAmino acids, peptides, and analogues
Intermediate Tree Nodes Amino acids and derivatives - Alpha amino acids and derivatives
Direct ParentValine and derivatives
Alternative Parents Alpha amino acids  Methyl-branched fatty acids  Amino acids  Monocarboxylic acids and derivatives  Carboxylic acids  Organopnictogen compounds  Organic oxides  Monoalkylamines  Hydrocarbon derivatives  Carbonyl compounds  
Molecular FrameworkAliphatic acyclic compounds
Substituents Valine or derivatives - Alpha-amino acid - Branched fatty acid - Methyl-branched fatty acid - Fatty acid - Fatty acyl - Amino acid - Carboxylic acid - Monocarboxylic acid or derivatives - Organopnictogen compound - Primary amine - Organooxygen compound - Organonitrogen compound - Organic nitrogen compound - Primary aliphatic amine - Carbonyl group - Organic oxygen compound - Amine - Organic oxide - Hydrocarbon derivative - Aliphatic acyclic compound
DescripciónThis compound belongs to the class of organic compounds known as valine and derivatives. These are compounds containing valine or a derivative thereof resulting from reaction of valine at the amino group or the carboxy group, or from the replacement of any hydrogen of glycine by a heteroatom.
External Descriptors non-proteinogenic alpha-amino acid
Estructura 3D
Modelo de Estructura Química Interactiva





Certificados (CoA, COO, BSE/TSE y tabla de análisis)
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.

6 results found

Lot NumberCertificate TypeFechaArticulo
K2123506Certificate of AnalysisSep 04, 2025 L102895
K2123515Certificate of AnalysisSep 04, 2025 L102895
K2124070Certificate of AnalysisSep 04, 2025 L102895
L2314073Certificate of AnalysisDec 22, 2023 L102895
H1908110Certificate of AnalysisMay 08, 2023 L102895
H1524044Certificate of AnalysisApr 13, 2023 L102895
Propiedades químicas y físicas
Punto de fusión (°C)299-301°C
Peso molecular131.170 g/mol
XLogP3-1.800
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count3
Rotatable Bond Count2
Exact Mass131.095 Da
Monoisotopic Mass131.095 Da
Topological Polar Surface Area63.300 Ų
Heavy Atom Count9
Formal Charge0
Complexity115.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count1
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Citations of This Product
Referencias
1. Yaohua Gu, Jiping Han, Ni Zhang, Weisong Yan, Yue Guo, Huiyi Tan, Changyi Yang, Fuke Wang, Huiqin Yao.  (2024)  Bimetallic Cu@Co-MOFs Mimic Peroxidase for Colorimetric Detection of Glutathione.  ACS Applied Nano Materials,      [PMID:] [10.1021/acsanm.4c04563]
Calculadoras de soluciones
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