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MilliporeSigma

T10200

Sigma-Aldrich

Tetradecylamine

95%

Sinónimos:

1-Aminotetradecane, Myristylamine

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About This Item

Fórmula lineal:
CH3(CH2)13NH2
Número de CAS:
Peso molecular:
213.40
Beilstein/REAXYS Number:
1633740
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

assay

95%

bp

162 °C/15 mmHg (lit.)

mp

38-40 °C (lit.)

SMILES string

CCCCCCCCCCCCCCN

InChI

1S/C14H31N/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15/h2-15H2,1H3

InChI key

PLZVEHJLHYMBBY-UHFFFAOYSA-N

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pictograms

Exclamation markEnvironment

signalword

Warning

Hazard Classifications

Aquatic Acute 1 - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

230.0 °F - closed cup

flash_point_c

110 °C - closed cup

ppe

dust mask type N95 (US), Eyeshields, Gloves


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Analytical sciences : the international journal of the Japan Society for Analytical Chemistry, 34(4), 501-504 (2018-04-13)
Therapeutic peptides and diagnostic agents with their molecular size below the renal clearance threshold suffer from short blood circulation time. Here, we report a novel design of peptide-based ligand with a strong binding affinity to human serum albumin (HSA), which
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Chemistry (Weinheim an der Bergstrasse, Germany), 23(39), 9397-9406 (2017-05-11)
Dual stimuli-responsive nanoparticles capable of fine-tuning drug release to augment therapeutic efficacy have become a promising tool for anticancer drug delivery. However, the rational design of these "smart" nanoparticles for a selective delivery and controlled release of multidrug combinations in
A M Salem et al.
Journal of clinical periodontology, 14(1), 44-47 (1987-01-01)
The surfactants tetradecylamine, hexadecylamine and chlorhexidine have been compared with regard to their ability to inhibit microbial growth. Antibacterial activity was assessed by tube dilution methods. Tetradecylamine and chlorhexidine were similar in antibacterial activity, being effective at low concentrations against
Lourdes Pérez et al.
International journal of molecular sciences, 21(23) (2020-12-02)
The surface activity, aggregates morphology, size and charge characteristics of binary catanionic mixtures containing a cationic amino acid-derived surfactant N(π), N(τ)-bis(methyl)-L-Histidine tetradecyl amide (DMHNHC14) and an anionic surfactant (the lysine-based surfactant Nα-lauroyl-Nεacetyl lysine (C12C3L) or sodium myristate) were investigated for

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