Boc-Asp-OtBu - ≥97% , CAS No.34582-32-6

CAS: 34582-32-6 Cat. No.: S136263 Molecular Weight: 289.325 Beilstein Registry Number: 4191700 EC Number: 840-509-2 PubChem CID: 7010517
AVAILABLE TO ORDER
GRADE & PURITY ≥97%
Synonyms
(s)-4-t-butoxy-3-(t-butoxycarbonylamino)-4-oxobutanoic acid | DS-1659 | NSC-5716 | AM20090540 | HY-W007573 | Boc-Asp-O-t-Butyl | 1-tert-Butyl N-Boc-L-aspartate | AKOS015892678 | 1-tert-Butyl N-(tert-Butoxycarbonyl)-L-aspartate | Boc-L-Aspartic acid 1-tert
Storage
Store at 2-8°C
Shipped In
Wet ice
 ·  off list, applied to all prices below.
Size
Status
Price
Qty
1g
S136263-1g
2
$9.90
5g
S136263-5g
2
$10.90
10g
S136263-10g
1

$12.90

$19.90
Save $7.00 (35.18%)
25g
S136263-25g
1

$29.90

$44.90
Save $15.00 (33.41%)
100g
S136263-100g
1

$118.90

$178.90
Save $60.00 (33.54%)
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Why this grade

≥97% 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.

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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.

Specifications

Synonyms
(s)-4-t-butoxy-3-(t-butoxycarbonylamino)-4-oxobutanoic acid | DS-1659 | NSC-5716 | AM20090540 | HY-W007573 | Boc-Asp-O-t-Butyl | 1-tert-Butyl N-Boc-L-aspartate | AKOS015892678 | 1-tert-Butyl N-(tert-Butoxycarbonyl)-L-aspartate | Boc-L-Aspartic acid 1-tert
Specifications & Purity
≥97%
Biochemical and Physiological Mechanisms
An aspartic acid derivative used in stereoselective synthesis
Storage
Store at 2-8°C
Shipped In
Wet ice
This product requires cold chain shipping. Ground and other economy services are not available.
Purity
≥97%
Names and Identifiers
Pubchem Sid488196022
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488196022
Canonical SmilesCC(C)(C)OC(=O)C(CC(=O)O)NC(=O)OC(C)(C)C
IUPAC Name(3S)-4-[(2-methylpropan-2-yl)oxy]-3-[(2-methylpropan-2-yl)oxycarbonylamino]-4-oxobutanoic acid
InChIKeyRAUQRYTYJIYLTF-QMMMGPOBSA-N
INCHI1S/C13H23NO6/c1-12(2,3)19-10(17)8(7-9(15)16)14-11(18)20-13(4,5)6/h8H,7H2,1-6H3,(H,14,18)(H,15,16)/t8-/m0/s1
Isomeric SMILES CC(C)(C)OC(=O)[C@H](CC(=O)O)NC(=O)OC(C)(C)C
WGK Germany 3
PubChem CID 7010517
Molecular Weight 289.325
Beilstein 4191700

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 ParentAspartic acid and derivatives
Alternative Parents Alpha amino acid esters  Fatty acid esters  Branched fatty acids  Dicarboxylic acids and derivatives  Carbamate esters  Carboxylic acid esters  Carboxylic acids  Organonitrogen compounds  Organic oxides  Hydrocarbon derivatives  Carbonyl compounds  
Molecular FrameworkAliphatic acyclic compounds
Substituents Aspartic acid or derivatives - Alpha-amino acid ester - Branched fatty acid - Fatty acid ester - Fatty acyl - Dicarboxylic acid or derivatives - Carbamic acid ester - Carboxylic acid ester - Carboxylic acid - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Hydrocarbon derivative - Organic oxide - Carbonyl group - Organic oxygen compound - Aliphatic acyclic compound
DescriptionThis compound belongs to the class of organic compounds known as aspartic acid and derivatives. These are compounds containing an aspartic acid or a derivative thereof resulting from reaction of aspartic acid 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.

9 results found

Lot NumberCertificate TypeDateItem
A2415523Certificate of AnalysisOct 27, 2025 S136263
A2415524Certificate of AnalysisOct 27, 2025 S136263
A2415525Certificate of AnalysisOct 27, 2025 S136263
A2415558Certificate of AnalysisOct 27, 2025 S136263
A2415559Certificate of AnalysisOct 27, 2025 S136263
D2321212Certificate of AnalysisFeb 07, 2025 S136263
D2321215Certificate of AnalysisFeb 07, 2025 S136263
D2321217Certificate of AnalysisFeb 07, 2025 S136263
E1528151Certificate of AnalysisJan 11, 2023 S136263
Chemical and Physical Properties
SolubilitySoluble in DMSO, Ethyl Acetate and Methanol
SensitivityHeat Sensitive
Specific Rotation[α]-24° (C=1.5,MeOH)
Melt Point(°C)103 °C
Molecular Weight289.320 g/mol
XLogP31.400
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count6
Rotatable Bond Count8
Exact Mass289.153 Da
Monoisotopic Mass289.153 Da
Topological Polar Surface Area102.000 Ų
Heavy Atom Count20
Formal Charge0
Complexity377.000
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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