Description

N-Boc-diethanolamine (CAS No. 103898-11-9) is a high-purity, protected amine derivative widely utilized in organic synthesis and pharmaceutical research. This compound, with the molecular formula C₉H₁₉NO₄ and IUPAC name tert-butyl N,N-bis(2-hydroxyethyl)carbamate, features a Boc (tert-butoxycarbonyl) protecting group, making it an essential intermediate for peptide coupling and other sensitive reactions. Its dual hydroxyl functionality allows for further derivatization, enabling the creation of complex molecular architectures. Ideal for researchers requiring reliable and consistent quality, our N-Boc-diethanolamine is rigorously tested to meet stringent purity standards, ensuring optimal performance in your applications.

Properties

• CAS Number: 103898-11-9
• Complexity: 170
• IUPAC Name: tert-butyl N,N-bis(2-hydroxyethyl)carbamate
• InChI: InChI=1S/C9H19NO4/c1-9(2,3)14-8(13)10(4-6-11)5-7-12/h11-12H,4-7H2,1-3H3
• InChI Key: KMUNFRBJXIEULW-UHFFFAOYSA-N
• Exact Mass: 205.13140809
• Molecular Formula: C9H19NO4
• Molecular Weight: 205.25
• SMILES: CC(C)(C)OC(=O)N(CCO)CCO
• Topological: 70
• Monoisotopic Mass: 205.13140809
• Synonyms: N-Boc-diethanolamine, 103898-11-9, DTXSID50402353, DTXCID80353208, 629-288-1, tert-Butyl bis(2-hydroxyethyl)carbamate, tert-Butyl N,N-bis(2-hydroxyethyl)carbamate, Boc-diethanolamine, MFCD01862953, (t-butoxy)-N,N-bis(2-hydroxyethyl)carboxamide, 1-Boc-diethanolamine, N-BOC diethanolamine, N-Boc-diethanolamine?, Carbamic acid, bis(2-hydroxyethyl)-, 1,1-dimethylethyl ester, SCHEMBL503444, KMUNFRBJXIEULW-UHFFFAOYSA-N, N-tert-butoxycarbonyldiethanolamine, AKOS009157236, tert-Butylbis(2-hydroxyethyl)carbamate, DS-5276, HY-W044078, BP-23153, DA-16045, N-Boc-diethanolamine, >=98.0% (GC), SY018071, t-butyl N,N-bis(2-hydroxyethyl)carbamate, CS-0037081, EN300-109429

Application

N-Boc-diethanolamine is commonly employed as a versatile building block in medicinal chemistry and peptide synthesis. Its Boc-protected amine group provides stability under acidic conditions, facilitating selective deprotection when needed. Researchers utilize this compound to synthesize modified amino acids, dendrimers, and other bioactive molecules. It is also valuable in polymer chemistry for creating functionalized polyols and crosslinking agents.

Safety and Hazards

GHS Hazard Statements

• H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]
• H319 (100%): Causes serious eye irritation [Warning Serious eye damage/eye irritation]
• H335 (97.4%): May cause respiratory irritation [Warning Specific target organ toxicity, single exposure; Respiratory tract irritation]

Precautionary Statements

• P261, P264, P264+P265, P271, P280, P302+P352, P304+P340, P305+P351+P338, P319, P321, P332+P317, P337+P317, P362+P364, P403+P233, P405, and P501

Hazard Classes and Categories

• Skin Irrit. 2 (100%)
• Eye Irrit. 2 (100%)
• STOT SE 3 (97.4%)

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Disclaimer: Sold exclusively for laboratory research. Prohibited for commercial use, diagnostics, or human/animal applications. Buyers assume all compliance liability.