33000
1,6-Diaminohexane
puriss., ≥99.0% (GC/T)
Synonym(s):
1,6-Hexanediamine, Hexamethylenediamine
Sign Into View Organizational & Contract Pricing
Select a Size
About This Item
Linear Formula:
NH2(CH2)6NH2
CAS Number:
Molecular Weight:
116.20
Beilstein:
1098307
EC Number:
MDL number:
UNSPSC Code:
12352100
grade
puriss.
Assay
≥99.0% (GC/T)
mp
39-42 °C
solubility
H2O: 0.1 g/mL, clear
SMILES string
NCCCCCCN
Looking for similar products? Visit Product Comparison Guide
Regulatory Information
新产品
This item has
Choose from one of the most recent versions:
Certificates of Analysis (COA)
Lot/Batch Number
It looks like we've run into a problem, but you can still download Certificates of Analysis from our Documents section.
If you need assistance, please contact Customer Support
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Richard F G Fröhlich et al.
Carbohydrate research, 346(12), 1592-1598 (2011-06-08)
Two simple and reliably accessible intermediates, N-carboxypentyl- and N-aminohexyl-1-deoxy-D-galactonojirimycin were employed for the synthesis of a set of terminally N-dansyl substituted derivatives. Reaction of the terminal carboxylic acid of N-carboxypentyl-1-deoxy-D-galactonojirimycin with N-dansyl-1,6-diaminohexane provided the chain-extended fluorescent derivative. Employing bis(6-dansylaminohexyl)amine, the
Linda G T Gaines et al.
Journal of environmental monitoring : JEM, 13(1), 119-127 (2010-10-28)
Although urinary 1,6-hexamethylene diamine (HDA) is a useful biomarker of exposure to 1,6-hexamethylene diisocyanate (HDI), a large degree of unexplained intra- and inter-individual variability exists between estimated HDI exposure and urine HDA levels. We investigated the effect of individual and
Surface synthesis of 2D branched polymer nanostructures.
Sigrid Weigelt et al.
Angewandte Chemie (International ed. in English), 47(23), 4406-4410 (2008-04-30)
Sheila L Flack et al.
The Annals of occupational hygiene, 54(1), 41-54 (2009-10-07)
Quantification of amines in biological samples is important for evaluating occupational exposure to diisocyanates. In this study, we describe the quantification of 1,6-hexamethylene diamine (HDA) levels in hydrolyzed plasma of 46 spray painters applying 1,6-hexamethylene diisocyanate (HDI)-containing paint in vehicle
Zhiming Zhang et al.
Inorganic chemistry, 47(17), 7615-7622 (2008-08-06)
The reaction between K 12[H 2P 2W 12O 48] and CuCl 2 in a NaCl aqueous solution assisted with organoamines (1,2-ethylenediamine (en), 1,6-hexamethylene diamine (hn), or both) leads to the isolation of three compounds: K 4Na 10[alpha 1-CuP 2W 17O
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service