247731
Hexamethylenediamine dihydrochloride
99%
Sinonimo/i:
1,6-Hexanediamine dihydrochloride
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About This Item
Formula condensata:
H2N(CH2)6NH2 · 2HCl
Numero CAS:
Peso molecolare:
189.13
Numero CE:
Numero MDL:
Codice UNSPSC:
12352100
ID PubChem:
NACRES:
NA.22
Prodotti consigliati
Livello qualitativo
Saggio
99%
Punto di fusione
256-257 °C (lit.)
Solubilità
water: freely soluble
Gruppo funzionale
amine
Stringa SMILE
Cl.Cl.NCCCCCCN
InChI
1S/C6H16N2.2ClH/c7-5-3-1-2-4-6-8;;/h1-8H2;2*1H
XMVQMBLTFKAIOX-UHFFFAOYSA-N
Descrizione generale
Toxicity of hexamethylenediamine dihydrochloride has been investigated. Hexamethylenediamine dihydrochloride is also known as 1,6-diaminohexane dihydrochloride, 1,6-hexamethylenediamine dihydrochloride, 1,6- hexylenediamine dihydrochloride or 1,6-diamino-n-hexane dihydrochloride. Hexamethylenediamine dihydrochloride on fusion of 1:6-di-(N3-cyano-N1-guanidino)-hexane yields polymeric diguanides.
Avvertenze
Warning
Indicazioni di pericolo
Consigli di prudenza
Classi di pericolo
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Organi bersaglio
Respiratory system
Codice della classe di stoccaggio
11 - Combustible Solids
Classe di pericolosità dell'acqua (WGK)
WGK 3
Punto d’infiammabilità (°F)
Not applicable
Punto d’infiammabilità (°C)
Not applicable
Dispositivi di protezione individuale
dust mask type N95 (US), Eyeshields, Gloves
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I clienti hanno visto anche
Charles Hebert
Toxicity report series, 24, 1-D8-1-D8 (1993-03-01)
1,6-Hexanediamine (HDA) is an aliphatic amine that is produced in large volumes in the United States. HDA is widely used as a corrosion inhibitor in lubricants and as an intermediate in the industrial synthesis of paints, resins, inks, and textiles.
850. Bisdiguanides having antibacterial activity.
Rose FL andSwain G.
Journal of the Chemical Society, 4422-4425 (1956)
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
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
Wei-Chiang Chen et al.
ACS applied materials & interfaces, 1(8), 1821-1826 (2010-04-02)
Solvent microenvironments are formed around individual single-walled carbon nanotubes (SWNTs) by mixing SWNT suspensions with water-immiscible organic solvents. These microenvironments are used to encapsulate the SWNTs with the monomer sebacoyl chloride. Hexamethylene diamine is then injected into the aqueous phase
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