362441
1-Hydroxybenzotriazole
<5% in H2O
Sign In to View Organizational & Contract Pricing.
Select a Size
Change View
About This Item
Empirical Formula (Hill Notation):
C6H5N3O
CAS Number:
Molecular Weight:
135.12
UNSPSC Code:
12352100
EC Number:
219-989-7
MDL number:
concentration
<5% in H2O
mp
156-159 °C (lit.)
SMILES string
On1nnc2ccccc12
Biochem/physiol Actions
Inhibits racemization in peptide syntheses using DCC as condensing agent.
signalword
Danger
hcodes
Hazard Classifications
Aquatic Chronic 3 - Expl. 1.3 - Eye Irrit. 2
Storage Class
1 - Explosive hazardous materials
wgk
WGK 1
ppe
dust mask type N95 (US), Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
flash_point_c
145 °C - Pensky Martens closed cup
flash_point_f
293.0 °F - Pensky Martens closed cup
Regulatory Information
新产品
This item has
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Tomoyo Suda et al.
Bioresource technology, 103(1), 498-501 (2011-11-11)
Tetracycline antibiotics are widely used in human and veterinary medicine; however, residual amounts of these antibiotics in the environment are of concern since they could contribute to selection of resistant bacteria. In this study, tetracycline (TC), chlortetracycline (CTC), doxycycline (DC)
Ping Wang et al.
Journal of the American Chemical Society, 132(47), 17045-17051 (2010-11-06)
Our global goal is that of synthesizing complex polypeptides and glycopeptides in homogeneous form. Chemistry-derived access to homogeneous biologics could well have useful consequences in the discovery of drugs and vaccines. The key finding in this study is that thio
Kumarasamy Murugesan et al.
Water research, 44(1), 298-308 (2009-10-27)
Triclosan (TCS), an antimicrobial agent, is an emerging and persistent environmental pollutant that is often found as a contaminant in surface waters and sediments; hence, knowledge of its degradability is important. In this study we investigated laccase-mediated TCS transformation and