N,N-Bis(2-hydroxyethyl)glycine, 99%, PH:4.0-6.0,Residue on Ignition:＜0.1

Name: N,N-Bis(2-hydroxyethyl)glycine, 99%, PH:4.0-6.0,Residue on Ignition:＜0.1 | 150-25-4
Brand: J&K Chemical
SKU: JK990589_100_G
Price: 329.8 USD
Availability: OutOfStock

Cat. No JK990589_100_G

Vendor: J&K Chemical

Product Information

Product Name

N,N-Bis(2-hydroxyethyl)glycine, 99%, PH:4.0-6.0,Residue on Ignition:＜0.1

Brand Name

J&K

Product Number

990589

CAS

150-25-4

Molecular Formula

C6H13NO4

Molecular Weight

163.17

SDS Document

View/Download

Certificate of Analysis (COA)

COA not found

General Information

Synonyms

N,N-Bis(2-hydroxyethyl)glycine

PubChem CID

8761

IUPAC Name

2-bis(2-hydroxyethyl)aminoacetic acid

InChI Key

FSVCELGFZIQNCK-UHFFFAOYSA-N

SMILES

C(CO)N(CCO)CC(=O)O

Properties

Melting Point

190

References Data Source From Pubchem

Kinetic and structural characterisation of domain‐specific angiotensin I‐converting enzyme inhibition by captopril, rentiapril and zofenoprilat

Publication Name: The FEBS Journal

Publication Date: 2026-02-03

DOI: 10.1111/febs.70428

Crystallographic fragment screening supports tool compound discovery and reveals conformational flexibility in human deoxyhypusine synthase

Publication Name: Communications Chemistry

Publication Date: 2026-01-17

DOI: 10.1038/s42004-026-01897-9

Structural analyses and substrate profiling of PPEP-3 provide new insights into the molecular basis of Pro-Pro endopeptidase specificity

Publication Name: iScience

Publication Date: 2026-01-16

DOI: 10.1016/j.isci.2025.114360

Autonomously Replicating Sequence-Bearing Plasmids Utilized in Pichia pastoris

Publication Name: Methods in molecular biology (Clifton, N.J.)

Publication Date: 2026

DOI: 10.1007/978-1-0716-4779-0_12

Exploiting Self-Processing 2A Peptides for Multigene Expression in Pichia pastoris

Publication Name: Methods in molecular biology (Clifton, N.J.)

Publication Date: 2026

DOI: 10.1007/978-1-0716-4779-0_18

N,N-Bis(2-hydroxyethyl)glycine, 99%, PH:4.0-6.0,Residue on Ignition:＜0.1

Product Information

General Information

Properties

References Data Source From Pubchem

Kinetic and structural characterisation of domain‐specific angiotensin I‐converting enzyme inhibition by captopril, rentiapril and zofenoprilat

Crystallographic fragment screening supports tool compound discovery and reveals conformational flexibility in human deoxyhypusine synthase

Structural analyses and substrate profiling of PPEP-3 provide new insights into the molecular basis of Pro-Pro endopeptidase specificity

Autonomously Replicating Sequence-Bearing Plasmids Utilized in Pichia pastoris

Exploiting Self-Processing 2A Peptides for Multigene Expression in Pichia pastoris