D16401
1,12-Diaminododecane
98%
Synonym(s):
1,12-Dodecanediamine, Dodecamethylenediamine
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About This Item
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Quality Level
Assay
98%
form
flakes
mp
67-69 °C (lit.)
SMILES string
NCCCCCCCCCCCCN
InChI
1S/C12H28N2/c13-11-9-7-5-3-1-2-4-6-8-10-12-14/h1-14H2
InChI key
QFTYSVGGYOXFRQ-UHFFFAOYSA-N
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Related Categories
Application
Feedstock for polymer synthesis. Source of twelve carbon chain for medicinal drugs.
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral - Skin Corr. 1B - Skin Sens. 1
Storage Class Code
8A - Combustible corrosive hazardous materials
WGK
WGK 1
Flash Point(F)
311.0 °F - closed cup
Flash Point(C)
155 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Chemical communications (Cambridge, England), 46(23), 4091-4093 (2010-05-19)
The X-ray crystal structure of 1,12-dodecane diammonium (C(12)DA(2+)) encapsulated in cucurbit[8]uril reveals an unconventional U-shaped conformation of C(12)DA(2+), which is attributed to the favorable host-guest interactions to overcome the charge-charge repulsion of the two ammonium groups in close proximity and
Monatshefte fur Chemie / Chemical Monthly, 124, 23-23 (1993)
Biochemistry international, 6(5), 627-633 (1983-05-01)
The acid phosphatase [EC 3.1.3.2] from human prostate gland is very unstable glycoprotein. To stabilize the enzyme cross-linking reaction with diamines was adopted. The carboxyl groups of the enzyme were activated with 1-ethyl-(3-dimethylaminopropyl)-carbodiimide and then treated with diamines of H2N-(CH2)n-NH2
Biochemistry, 48(7), 1508-1516 (2009-02-10)
Mammalian polyamine oxidases (PAOs) catalyze the oxidation of N1-acetylspermine and N1-acetylspermidine to produce N-acetyl-3-aminopropanaldehyde and spermidine or putrescine. Structurally, PAO is a member of the monoamine oxidase family of flavoproteins. The effects of pH on the kinetic parameters of mouse
Biophysical journal, 74(2 Pt 1), 722-730 (1998-04-09)
In this study we compared polyamines to various diamines, and we modeled flexibility as well as hydrophobicity properties of these molecules to examine possible structural differences that could explain their external effects on the channels. The natural polyamines (putrescine, cadaverine
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