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105198

Sigma-Aldrich

(+)-Dehydroabietylamine

technical grade, 60%

Sinónimos:

1,4a-Dimethyl-7-isopropyl-1,2,3,4,4a,9,10,10a-octahydro-1-phenanthrenemethylamine

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About This Item

Fórmula empírica (notación de Hill):
C20H31N
Número de CAS:
1446-61-3
Peso molecular:
285.47
Beilstein/REAXYS Number:
3084620
EC Number:
215-899-7
MDL number:
MFCD00213430
UNSPSC Code:
12352116
PubChem Substance ID:
24846693
NACRES:
NA.22

grade

technical grade

optical activity

[α]20/D +56.1°, c = 2.4 in pyridine

composition

high molecular weight primary amines, 90%

concentration

60%

refractive index

n20/D 1.546 (lit.)

SMILES string

[H][C@@]12CCc3cc(ccc3[C@@]1(C)CCC[C@@]2(C)CN)C(C)C

InChI

1S/C20H31N/c1-14(2)15-6-8-17-16(12-15)7-9-18-19(3,13-21)10-5-11-20(17,18)4/h6,8,12,14,18H,5,7,9-11,13,21H2,1-4H3/t18-,19-,20+/m0/s1

InChI key

JVVXZOOGOGPDRZ-SLFFLAALSA-N

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pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

10 - Combustible liquids

wgk_germany

WGK 3

flash_point_f

235.4 °F - closed cup

flash_point_c

113 °C - closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

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Muhammad Ayaz Mustufa et al.
BMC cancer, 16(1), 883-883 (2016-11-16)
The purpose of present work is to synthesize novel (+)-Dehydroabietylamine derivatives (DAAD) using N-acetyl-α-amino acid conjugates and determine its cytotoxic effects on hepatocellular carcinoma cells. An analytical study was conducted to explore cytotoxic activity of DAAD on hepatocellular carcinoma cell
Tiina Laaksonen et al.
Molecules (Basel, Switzerland), 20(11), 20873-20886 (2015-11-28)
Chiral tertiary and quaternary amine solvating agents for NMR spectroscopy were synthesized from the wood resin derivative (+)-dehydroabietylamine (2). The resolution of enantiomers of model compounds [Mosher's acid (3) and its n-Bu₄N salt (4)] (guests) by (+)-dehydroabietyl-N,N-dimethylmethanamine (5) and its

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