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Key Documents

D144401

Sigma-Aldrich

3-Dimethylamino-1-propanol

99%

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About This Item

Linear Formula:
(CH3)2N(CH2)3OH
CAS Number:
Molecular Weight:
103.16
Beilstein:
1732032
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

99%

form

liquid

refractive index

n20/D 1.436 (lit.)

bp

163-164 °C (lit.)

density

0.872 g/mL at 25 °C (lit.)

SMILES string

CN(C)CCCO

InChI

1S/C5H13NO/c1-6(2)4-3-5-7/h7H,3-5H2,1-2H3

InChI key

PYSGFFTXMUWEOT-UHFFFAOYSA-N

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Signal Word

Danger

Hazard Statements

Hazard Classifications

Acute Tox. 4 Oral - Eye Dam. 1 - Flam. Liq. 3 - Skin Corr. 1B

Storage Class Code

3 - Flammable liquids

WGK

WGK 1

Flash Point(F)

105.8 °F - closed cup

Flash Point(C)

41 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Song Yang Khor et al.
Small (Weinheim an der Bergstrasse, Germany), 14(34), e1801702-e1801702 (2018-07-26)
The size and surface chemistry of nanoparticles dictate their interactions with biological systems. However, it remains unclear how these key physicochemical properties affect the cellular association of nanoparticles under dynamic flow conditions encountered in human vascular networks. Here, the facile
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A Q Zhang et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 36(11), 923-927 (1998-10-15)
Dimethylamine is the immediate precursor of dimethylnitrosamine, a known potent carcinogen in a wide variety of animal species. Although small amounts of dimethylamine are ingested directly, the major dietary source is believed to be via choline and related materials. Owing
Amin GhavamiNejad et al.
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A multifunctional hydrogel that combines the dual functionality of both antifouling and antimicrobial capacities holds great potential for many bioapplications. Many approaches and different materials have been employed to synthesize such a material. However, a systematic study, including in vitro
Werner J Geldenhuys et al.
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The high affinity neuronal choline transporter (CHT1) is responsible for the uptake of choline into the pre-synaptic terminal of cholinergic neurons. Considering our past experience with modeling the blood-brain barrier choline transporter (BBBCHT) as drug delivery vector to the CNS

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