D-tert-Leucine - ≥98% , CAS No.26782-71-8

CAS: 26782-71-8 Cat. No.: D115672 Molecular Weight: 131.17 Beilstein Registry Number: 1721830 EC Number: 607-998-2
AVAILABLE TO ORDER
GRADE & PURITY ≥98%
Synonyms
(R)-2-Amino-3,3-dimethylbutyric acid | D-tert-Leucine, 98% | D-Valine, 3-methyl- | AC-24096 | BCP09236 | AM20090329 | (r)-tert-leucine | D-t-Butylglycine | (2R)-2-amino-3,3-dimethylbutyric acid | AKOS006240276 | UNII-P3L3QZA16M | (r)-tert-butylglycine | (
Storage
Room temperature
Shipped In
Normal
 ·  off list, applied to all prices below.
Size
Status
Price
Qty
250mg
D115672-250mg
3
$9.90
1g
D115672-1g
5
$10.90
5g
D115672-5g
5

$13.90

$20.90
Save $7.00 (33.49%)
10g
D115672-10g
4

$26.90

$40.90
Save $14.00 (34.23%)
25g
D115672-25g
3

$58.90

$88.90
Save $30.00 (33.75%)
100g
D115672-100g
1

$187.90

$281.90
Save $94.00 (33.35%)
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Why this grade

≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Room temperature Ships Normal 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 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Overview

Product Application:

D-tert-Leucine is used for synthesis of amino acids e.g. in the synthesis of aldehydes by double alkylation of unsaturated aldimines of tert-Leu esters.

Specifications

Synonyms
(R)-2-Amino-3, 3-dimethylbutyric acid | D-tert-Leucine, 98% | D-Valine, 3-methyl- | AC-24096 | BCP09236 | AM20090329 | (r)-tert-leucine | D-t-Butylglycine | (2R)-2-amino-3, 3-dimethylbutyric acid | AKOS006240276 | UNII-P3L3QZA16M | (r)-tert-butylglycine | (
Specifications & Purity
≥98%
Storage
Room temperature
Shipped In
Normal
Purity
≥98%
Names and Identifiers
Pubchem Sid504764395
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504764395
Canonical SmilesCC(C)(C)C(C(=O)O)N
IUPAC Name(2R)-2-amino-3,3-dimethylbutanoic acid
InChIKeyNPDBDJFLKKQMCM-BYPYZUCNSA-N
INCHI1S/C6H13NO2/c1-6(2,3)4(7)5(8)9/h4H,7H2,1-3H3,(H,8,9)/t4-/m0/s1
Isomeric SMILES CC(C)(C)[C@H](C(=O)O)N
WGK Germany 3
Molecular Weight 131.17
Beilstein 1721830
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
ClassCarboxylic 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 D-alpha-amino acids  Methyl-branched fatty acids  Quaternary ammonium salts  Carboxylic acid salts  Amino acids  Monocarboxylic acids and derivatives  Carboxylic acids  Organic zwitterions  Organic salts  Organic oxides  Monoalkylamines  Hydrocarbon derivatives  Carbonyl compounds  
Molecular FrameworkAliphatic acyclic compounds
Substituents Valine or derivatives - Alpha-amino acid - D-alpha-amino acid - Branched fatty acid - Methyl-branched fatty acid - Fatty acid - Fatty acyl - Quaternary ammonium salt - Amino acid - Carboxylic acid salt - Carboxylic acid - Monocarboxylic acid or derivatives - Hydrocarbon derivative - Primary amine - Organooxygen compound - Organonitrogen compound - Organic oxide - Primary aliphatic amine - Organic zwitterion - Organic salt - Carbonyl group - Organic oxygen compound - Amine - Organic nitrogen compound - Aliphatic acyclic compound
DescriptionThis 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 Not available
3D Structure
Interactive Chemical Structure Model





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.

11 results found

Lot NumberCertificate TypeDateItem
G2228346Certificate of AnalysisMay 19, 2026 D115672
G2228347Certificate of AnalysisMay 19, 2026 D115672
G2228349Certificate of AnalysisMay 19, 2026 D115672
G2207092Certificate of AnalysisApr 07, 2026 D115672
K1709014Certificate of AnalysisJun 12, 2025 D115672
C1320061Certificate of AnalysisOct 11, 2024 D115672
D2425182Certificate of AnalysisMar 21, 2024 D115672
D2425311Certificate of AnalysisMar 21, 2024 D115672
F2316958Certificate of AnalysisJul 12, 2022 D115672
F2316952Certificate of AnalysisJun 12, 2022 D115672
H2529073Certificate of AnalysisJun 12, 2022 D115672

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Chemical and Physical Properties
Specific Rotation[α]9° (C=3,H2O)
Melt Point(°C)≥300°C
Molecular Weight131.170 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 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
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