1,10-Diaminodecane

Product Information

Molecular Formula:
C10H24N2
Molecular Weight:
172.31
Description
1,10-Diaminodecane (CAS# 646-25-3) is used in manufacturing method of polyimide powder.
Synonyms
decane-1,10-diamine
IUPAC Name
decane-1,10-diamine
Canonical SMILES
C(CCCCCN)CCCCN
InChI
InChI=1S/C10H24N2/c11-9-7-5-3-1-2-4-6-8-10-12/h1-12H2
InChI Key
YQLZOAVZWJBZSY-UHFFFAOYSA-N
Boiling Point
140 ℃12 mmHg (lit.)
Melting Point
62 ℃
Purity
98 %
Density
14012 g/cm3
Appearance
White to orange to green powder to crystal
Application
Used as a co-monomer in polyamide production; Permitted for making articles designed for repeated food contact; Used as a monomer for plastic products.
Refractive Index
1.6210 (estimate)
LogP
3.42520

Safety Information

Hazards
H314:
Causes severe skin burns and eye damage.
Precautionary Statement
P260, P264, P270, P280, P301+P312, P301+P330+P331, P303+P361+P353, P304+P340, P305+P351+P338, P310, P321, P330, P363, P405, and P501
Signal Word
Danger

Computed Properties

XLogP3
1.9
Hydrogen Bond Donor Count
2
Hydrogen Bond Acceptor Count
2
Rotatable Bond Count
9
Exact Mass
172.193948774 g/mol
Monoisotopic Mass
172.193948774 g/mol
Topological Polar Surface Area
52Ų
Heavy Atom Count
12
Formal Charge
0
Complexity
64.2
Isotope Atom Count
0
Defined Atom Stereocenter Count
0
Undefined Atom Stereocenter Count
0
Defined Bond Stereocenter Count
0
Undefined Bond Stereocenter Count
0
Covalently-Bonded Unit Count
1
Compound Is Canonicalized
Yes

Patents

Publication Number Title Priority Date
CN-114149590-A Production process of polyether amide elastomer 2021-12-28
CN-114181390-A Bio-based high-temperature-resistant polyamide and preparation method thereof 2021-12-23
CN-114163812-A Low-temperature-resistant high-wear-resistance nylon material and preparation method and application thereof 2021-12-20
CN-113999392-A Diamine-modified copolyamide and preparation method thereof 2021-12-15
CN-114015011-A Polyurethane composition and preparation method and application thereof 2021-12-14
CN-114058008-A Process for preparing semi-aromatic polyamides end-capped with monocarboxylic acids, semi-aromatic polyamides and molding compositions 2021-12-13
CN-114058009-A Process for preparing semi-aromatic polyamides with reduced loss of diamine monomer, semi-aromatic polyamides and molding compositions 2021-12-13
CN-114058010-A Process for preparing low-energy semiaromatic polyamides, semiaromatic polyamides and moulding compositions 2021-12-13
CN-114133559-A Process for preparing semiaromatic polyamides with reduced salt formation cycle, semiaromatic polyamides and moulding compositions 2021-12-13
CN-113980338-A Thermoplastic polyurethane foaming particles, preparation method and application thereof in low-temperature bending resistant sole material 2021-12-09

Literatures

PMID Publication Date Title Journal
21907525 2011-11-01 Synthesis, cytotoxicity, and in vitro antileishmanial activity of mono-t-butyloxycarbonyl-protected diamines Diagnostic microbiology and infectious disease
22220025 2011-11-01 Decane-1,10-diaminium dinitrate Acta crystallographica. Section E, Structure reports online
22413310 2011-11-01 Preparation and electrochemical and electrocatalytic properties of nanocomposite multilayer film based on a Keggin-type phosphomolybdate Journal of nanoscience and nanotechnology
20057956 2009-11-20 Köln-Timişoara Molecular activity combined models toward interspecies toxicity assessment International journal of molecular sciences
19705394 2009-10-05 Guest-directed supramolecular architectures of {W36} polyoxometalate crowns Chemistry, an Asian journal
19734910 2009-10-01 Genetic mapping of targets mediating differential chemical phenotypes in Plasmodium falciparum Nature chemical biology
16004467 2005-07-01 Novel agmatine-containing poly(amidoamine) hydrogels as scaffolds for tissue engineering Biomacromolecules
15276032 2004-09-01 Adsorption of Co(II), Ni(II), Cu(II), and Zn(II) on hexagonal templated zirconia obtained thorough a sol-gel process: the effects of nanostructure on adsorption features Journal of colloid and interface science
14572240 2003-10-30 Inclusion networks of a calix[5]arene-based exoditopic receptor and long-chain alkyldiammonium ions Organic letters
12740427 2003-07-01 Inward rectification by polyamines in mouse Kir2.1 channels: synergy between blocking components The Journal of physiology
The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

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