Boc-Dap-OH - ≥97% , CAS No.73259-81-1

CAS: 73259-81-1 Cat. No.: B102447 Fórmula: C8H16N2O4 Peso molecular: 204.22 Beilstein Registry Number: 4182136
Disponible para pedir
GRADE & PURITY ≥97%
Synonyms
(s)-3-amino-2-boc-aminopropanoic acid | N(alpha)-boc-L-2,3-diaminopropionic acid | (2S)-3-amino-2-[[(tert-butoxy)carbonyl]amino]propanoic acid | (2S)-3-azaniumyl-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoate | HY-W008325 | (S)-3-Amino-2-((tert-butox
Storage
Argon charged,Room temperature
Shipped In
Normal
★
Size
Alemania (EU)
USA*
Price
Qty
1g
B102447-1g
—
5 Disponible

8,59€

12,93€
Guardar 4,34 € (33.56%)
5g
B102447-5g
—
4 Disponible

10,33€

15,53€
Guardar 5,21 € (33.52%)
10g
B102447-10g
Fabricado bajo pedido · 8–12 semanas

19,87€

30,28€
Guardar 10,41 € (34.38%)
25g
B102447-25g
—
4 Disponible

46,77€

70,20€
Guardar 23,43 € (33.37%)
100g
B102447-100g
—
1 Disponible

176,93€

265,44€
Guardar 88,51 € (33.34%)
Enter a quantity for the sizes you want to add.
🧪

Why this grade

≥97% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Argon charged,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.

Descripción general

Reactant for: ? Protein assembly directed by synthetic molecular recognition motifs ? Solid phase synthesis of gramicidin S cyclic analogs with antibiotic and hemolytic activities? Synthesis of HCV protease inhibitor modified analogs ? Solid phase synthesis of peptidic V1a receptor agonists ? Directed peptide assembly at lipid-water interface

Specifications

Sinónimos
(s)-3-amino-2-boc-aminopropanoic acid | N(alpha)-boc-L-2,3-diaminopropionic acid | (2S)-3-amino-2-[[(tert-butoxy)carbonyl]amino]propanoic acid | (2S)-3-azaniumyl-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoate | HY-W008325 | (S)-3-Amino-2-((tert-butox
Especificaciones y pureza
≥97%
Condiciones de almacenamiento de almacenamiento
Argon charged,Room temperature
Enviado en
Normal
Pureza
≥97%
Nombres e identificadores
Pubchem Sid488192975
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488192975
Sonrisas canónicasCC(C)(C)OC(=O)NC(CN)C(=O)O
IUPAC Name(2S)-3-amino-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoic acid
InChIKeyKRJLRVZLNABMAT-YFKPBYRVSA-N
INCHI1S/C8H16N2O4/c1-8(2,3)14-7(13)10-5(4-9)6(11)12/h5H,4,9H2,1-3H3,(H,10,13)(H,11,12)/t5-/m0/s1
Isómeros SMILES CC(C)(C)OC(=O)N[C@@H](CN)C(=O)O
WGK Alemania 3
Peso molecular 204.22
Beilstein 4182136
Reaxy-Rn 8054362
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=8054362&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
Direct ParentAlpha amino acids and derivatives
Alternative Parents Carbamate esters  Organic carbonic acids and derivatives  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 or derivatives - Carbamic acid ester - Carbonic acid derivative - Amino acid - Carboxylic acid - Monocarboxylic acid or derivatives - Organopnictogen compound - Primary amine - Organooxygen compound - Organonitrogen compound - Organic oxygen compound - Organic nitrogen compound - Primary aliphatic amine - Carbonyl group - Amine - Hydrocarbon derivative - Organic oxide - Aliphatic acyclic compound
DescripciónThis compound belongs to the class of organic compounds known as alpha amino acids and derivatives. These are amino acids in which the amino group is attached to the carbon atom immediately adjacent to the carboxylate group (alpha carbon), or a derivative thereof.
External Descriptors Not available
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.

10 results found

Lot NumberCertificate TypeFechaArticulo
L2213117Certificate of AnalysisSep 07, 2026 B102447
L2213133Certificate of AnalysisSep 07, 2026 B102447
K2229213Certificate of AnalysisSep 02, 2026 B102447
E1315061Certificate of AnalysisJan 17, 2025 B102447
D1614026Certificate of AnalysisDec 12, 2023 B102447
K2320160Certificate of AnalysisNov 30, 2023 B102447
C2309104Certificate of AnalysisMar 16, 2023 B102447
C2309102Certificate of AnalysisMar 14, 2023 B102447
C1802070Certificate of AnalysisJan 19, 2022 B102447
C1802071Certificate of AnalysisJan 19, 2022 B102447
Propiedades químicas y físicas
SensibilidadAir Sensitive
Rotación específica [α]-5° (C=1,AcOH)
Punto de fusión (°C)210°C
Peso molecular204.220 g/mol
XLogP3-2.700
Hydrogen Bond Donor Count3
Hydrogen Bond Acceptor Count5
Rotatable Bond Count5
Exact Mass204.111 Da
Monoisotopic Mass204.111 Da
Topological Polar Surface Area102.000 Ų
Heavy Atom Count14
Formal Charge0
Complexity222.000
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
Calculadoras de soluciones
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