JavaScript seems to be disabled in your browser. For the best experience on our site, be sure to turn on Javascript in your browser.

This is a demo store. No orders will be fulfilled.

Account

Settings

Language

྾

Home
Chemistry & Biochemicals
Biochemicals
Amino Acids
Boc-Asn-OH - ≥98.5% (T), high purity , CAS No.7536-55-2

Skip to the end of the images gallery

Skip to the beginning of the images gallery

Boc-Asn-OH - ≥98.5% (T), high purity , CAS No.7536-55-2

2 Citations

COA

Grade & Purity:

≥98.5%(T)

Cas Number: 7536-55-2
Molecular Weight: 232.23
Beilstein Registry Number: 1977963
EC Number: 231-405-2
MDL number: MFCD00038152
PubChem CID: 82035
PubChem SID: 488186037

In stock

Item Number

B113133

Grouped product items
SKU	Size	Availability	Price
B113133-5g	5g	5	$18.90
B113133-10g	10g	3	$28.90
B113133-25g	25g	3	$64.90
B113133-100g	100g	2	$230.90
B113133-500g	500g	Available within 4-8 weeks(?) Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!	$1,038.90

View related series

Chemical Biology (1255) N-protected amino acids (344)

Basic Description

Synonyms	Boc-L-asparagine \| N~2~-(tert-butoxycarbonyl)-L-asparagine \| (2S)-4-amino-2-[(2-methylpropan-2-yl)oxycarbonylamino]-4-oxobutanoic acid \| EINECS 231-405-2 \| N2-((1,1-Dimethylethoxy)carbonyl)-L-asparagine \| L-Asparagine, N(2)-[(1,1-dimethylethoxy)carbonyl]-
Specifications & Purity	≥98.5%(T)
Shipped In	Normal

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Organic acids and derivatives
  - Class Carboxylic acids and derivatives
    - Subclass Amino acids, peptides, and analogues
      - Level5 Amino acids and derivatives
        Level6 Alpha amino acids and derivatives

Kingdom	Organic compounds
Superclass	Organic acids and derivatives
Class	Carboxylic acids and derivatives
Subclass	Amino acids, peptides, and analogues
Intermediate Tree Nodes	Amino acids and derivatives
Direct Parent	Alpha amino acids and derivatives
Alternative Parents	Branched fatty acids Propargyl-type 1,3-dipolar organic compounds Monocarboxylic acids and derivatives Carboxylic acids Carboximidic acids Organopnictogen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds
Molecular Framework	Aliphatic acyclic compounds
Substituents	Alpha-amino acid or derivatives - Branched fatty acid - Fatty acid - Fatty acyl - Carboximidic acid - Carboximidic acid derivative - Carboxylic acid - Monocarboxylic acid or derivatives - Propargyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Organonitrogen compound - Carbonyl group - Organic oxygen compound - Organooxygen compound - Organic nitrogen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Aliphatic acyclic compound
Description	This 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	L-asparagine derivative
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61. DOI: 10.1186/s13321-016-0174-y

Mechanisms of Action

Mechanism of Action	Action Type	target ID	Target Name	Target Type	Target Organism	Binding Site Name	References

Names and Identifiers

Pubchem Sid	488186037
Pubchem Sid Url	https://pubchem.ncbi.nlm.nih.gov/substance/488186037
IUPAC Name	(2S)-4-amino-2-[(2-methylpropan-2-yl)oxycarbonylamino]-4-oxobutanoic acid
INCHI	InChI=1S/C9H16N2O5/c1-9(2,3)16-8(15)11-5(7(13)14)4-6(10)12/h5H,4H2,1-3H3,(H2,10,12)(H,11,15)(H,13,14)/t5-/m0/s1
InChIKey	FYYSQDHBALBGHX-YFKPBYRVSA-N
Smiles	CC(C)(C)OC(=O)NC(CC(=O)N)C(=O)O
Isomeric SMILES	CC(C)(C)OC(=O)N[C@@H](CC(=O)N)C(=O)O
WGK Germany	3
Molecular Weight	232.23
Beilstein	1977963
Reaxy-Rn	2216416
Reaxys-RN_link_address	https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2216416&ln=

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.

8 results found

Lot Number	Certificate Type	Date	Item
I2022155	Certificate of Analysis	Jul 03, 2024	B113133
I2022154	Certificate of Analysis	Jul 03, 2024	B113133
A2220077	Certificate of Analysis	Jan 04, 2022	B113133
A2220134	Certificate of Analysis	Jan 04, 2022	B113133
A2221017	Certificate of Analysis	Jan 04, 2022	B113133
A2220076	Certificate of Analysis	Jan 04, 2022	B113133
E2325111	Certificate of Analysis	Jan 04, 2022	B113133
A2220073	Certificate of Analysis	Jan 04, 2022	B113133

Chemical and Physical Properties

Specific Rotation[α]	-7 ° (C=1, DMF)
Melt Point(°C)	173-175°C
Molecular Weight	232.230 g/mol
XLogP3	-0.600
Hydrogen Bond Donor Count	3
Hydrogen Bond Acceptor Count	5
Rotatable Bond Count	6
Exact Mass	232.106 Da
Monoisotopic Mass	232.106 Da
Topological Polar Surface Area	119.000 Å²
Heavy Atom Count	16
Formal Charge	0
Complexity	295.000
Isotope Atom Count	0
Defined Atom Stereocenter Count	1
Undefined Atom Stereocenter Count	0
Defined Bond Stereocenter Count	0
Undefined Bond Stereocenter Count	0
The total count of all stereochemical bonds	0
Covalently-Bonded Unit Count	1

Citations of This Product

How to Cite Aladdin Scientific Products?

1. Zhanpeng Ren, Jianying Wang, Chenglong Xue, Minghua Deng, Haiyang Yu, Tianci Lin, Jiayuan Zheng, Rongxiang He, Xianbao Wang, Jinhua Li. (2023) Ultrahighly Sensitive and Selective Glutathione Sensor Based on Carbon Dot-Functionalized Solution-Gate Graphene Transistor. ANALYTICAL CHEMISTRY, 95 (48): (17750–17758).
2. Yuting Li, Xiaotong Li, Jinshun Ye, Zhenzhao Weng, Xiaozhen Liu, Fengyuan Liu, Jingkun Yan, Lin Li. (2024) Reactivity of amino acid residues towards 4-methylbenzoquinone: Effect on the site-specificity of quinone-protein reaction. LWT-FOOD SCIENCE AND TECHNOLOGY, 200 (116217).

Solution Calculators

Molarity Calculator

Determine the necessary mass, volume, or concentration for preparing a solution.

Mass

Concentration

Volume

M. Wt*

g/mol

*When preparing stock solutions, always use the batch-specific molecular weight of the product found on the vial label and the Certificate of Analysis (available online).

Dilution Calculator

Determine the dilution needed to prepare a stock solution.

Concentration 1 (C1)

Volume 1 (V1)

Concentration 2 (C2)

Volume 2 (V2)

Reconstitution Calculator

The reconstitution calculator enables you to quickly determine the volume of a reagent needed to reconstitute your vial. Just enter the mass of the reagent and the target concentration, and the calculator will do the rest.

Volume (to add to vial)

Mass (in vial)

Desired Reconstitution Concentration

Reviews

Shall we send you a message when we have discounts available?

Remind me later

Thank you! Please check your email inbox to confirm.

Oops! Notifications are disabled.