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105198

Sigma-Aldrich

(+)-Dehydroabietylamine

technical grade, 60%

Synonym(s):

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

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About This Item

Empirical Formula (Hill Notation):
C20H31N
CAS Number:
1446-61-3
Molecular Weight:
285.47
Beilstein:
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

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

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

Target Organs

Respiratory system

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

235.4 °F - closed cup

Flash Point(C)

113 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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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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