1,12-Diaminododecane

Product Information

Molecular Formula:
C12H28N2
Molecular Weight:
200.36
Description
1,12-Diaminododecane (CAS# 2783-17-7) is a long aliphatic diamine that is known to inhibit specific phospholipid-sensitive enzymes and myosin light-chain kinases.
Synonyms
dodecane-1,12-diamine
IUPAC Name
dodecane-1,12-diamine
Canonical SMILES
C(CCCCCCN)CCCCCN
InChI
InChI=1S/C12H28N2/c13-11-9-7-5-3-1-2-4-6-8-10-12-14/h1-14H2
InChI Key
QFTYSVGGYOXFRQ-UHFFFAOYSA-N
Boiling Point
304 °C
Melting Point
67-69 °C (lit.)
Flash Point
311 °F
Density
0.856 g/cm3
Appearance
White crystalline solid
Refractive Index
1.4383 (estimate)
LogP
4.20540

Safety Information

Hazards
H302:
Harmful if swallowed.
H315:
Causes skin irritation.
H317:
May cause an allergic skin reaction.
H319:
Causes serious eye irritation.
H331:
Toxic if inhaled.
H400:
Very toxic to aquatic life.
Precautionary Statement
P260, P261, P264, P270, P272, P280, P301+P312, P301+P330+P331, P302+P352, P303+P361+P353, P304+P340, P305+P351+P338, P310, P321, P330, P332+P313, P333+P313, P362, P363, P405, and P501
Signal Word
Danger

Computed Properties

XLogP3
3
Hydrogen Bond Donor Count
2
Hydrogen Bond Acceptor Count
2
Rotatable Bond Count
11
Exact Mass
200.225248902 g/mol
Monoisotopic Mass
200.225248902 g/mol
Topological Polar Surface Area
52Ų
Heavy Atom Count
14
Formal Charge
0
Complexity
82.3
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

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CN-114149590-A Production process of polyether amide elastomer 2021-12-28
CN-114106716-A Adhesive interlining suitable for knitted cashmere fabric and preparation method thereof 2021-12-22
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-114133560-A Process for preparing semiaromatic polyamides with improved impact strength, semiaromatic polyamides and moulding compositions 2021-12-13
CN-114106319-A Method for continuously preparing polyamide with low gel content and narrow molecular weight distribution and product thereof 2021-11-18
CN-113896863-A Epoxy resin glass high polymer material, three-component epoxy solution, preparation method and application 2021-11-09

Literatures

PMID Publication Date Title Journal
22802135 2012-10-01 A chemical proteomics approach reveals Hsp27 as a target for proapoptotic clerodane diterpenes Molecular bioSystems
22907920 2012-09-24 Absolute stereochemical determination of chiral carboxylates using an achiral molecular tweezer Chemistry (Weinheim an der Bergstrasse, Germany)
22440050 2012-06-01 Diaminododecane-based cationic bolaamphiphile as a non-viral gene delivery carrier Biomaterials
21907525 2011-11-01 Synthesis, cytotoxicity, and in vitro antileishmanial activity of mono-t-butyloxycarbonyl-protected diamines Diagnostic microbiology and infectious disease
21190372 2011-03-03 Molecular recognition of melamine by vesicles spontaneously formed from orotic acid derived bolaamphiphiles The journal of physical chemistry. B
21969739 2010-11-01 Polymers for colon targeted drug delivery Indian journal of pharmaceutical sciences
20480073 2010-06-21 Unconventional U-shaped conformation of a bolaamphiphile embedded in a synthetic host Chemical communications (Cambridge, England)
20148228 2010-02-27 Cucurbit[10]uril binding of dinuclear platinum(II) and ruthenium(II) complexes: association/dissociation rates from seconds to hours Dalton transactions (Cambridge, England : 2003)
19705394 2009-10-05 Guest-directed supramolecular architectures of {W36} polyoxometalate crowns Chemistry, an Asian journal
19715361 2009-09-01 In situ studies of soft- and reactive landing of mass-selected ions using infrared reflection absorption spectroscopy Analytical chemistry
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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