Cas no 1740-19-8 (Dehydroabietic acid)

Dehydroabietic acid is a diterpenoid compound derived from rosin, primarily obtained through the dehydrogenation of abietic acid. It is characterized by its aromatic structure and stability, making it valuable in various industrial applications. Key advantages include its role as a versatile intermediate in the synthesis of specialty chemicals, such as resins, adhesives, and coatings, where its rigid molecular structure enhances thermal and oxidative resistance. Additionally, it exhibits antimicrobial properties, broadening its utility in preservative formulations. Its low toxicity and biodegradability further support its use in environmentally sensitive applications. Dehydroabietic acid is also studied for potential pharmaceutical uses due to its bioactive properties.

Dehydroabietic acid structure

Product Name:Dehydroabietic acid

CAS No:1740-19-8

MF:C₂₀H₂₈O₂

MW:300.435126304626

MDL:MFCD09839012

CID:140649

PubChem ID:94391

Update Time:2025-06-07

Dehydroabietic acid Chemical and Physical Properties

Names and Identifiers

- 1-Phenanthrenecarboxylicacid, 1,2,3,4,4a,9,10,10a-octahydro-1,4a-dimethyl-7-(1-methylethyl)-,(1R,4aS,10aR)-
- Dehydroabietlc acid
- 1-Phenanthrenecarboxylicacid, 1,2,3,4,4a,9,10,10a-octahydro-1,4a-dimethyl-7-(1-methylethyl)-,(...
- Dehydroabieticacid
- 1,2,3,4,4a,9,10,10a-Octahydro-1,4a-dimethyl-7-(1-methylethyl)-1-phenanthrenecarboxylic acid
- Abieta-8,11,13-trien-18-oic acid,Dehydroabietate
- (+)-Dehydroabietic acid
- Abieta-8,11,13-trien-18-oic acid
- (1R,4aS,10aR)-1,2,3,4,4a,9,10,10a-Octahydro-1,4a-dimethyl-7-(1-methylethyl)-1-phenanthrenecarboxylic acid
- [ "" ]
- NSC 2952
- Dehydroabietate
- dehydro-abieticaci
- 8,11,13-Abietatriene-18-oic acid
- 1-PHENANTHRENECARBOXYLICACID,1,2,
- abieta-8(14),9(11),12-trien-18-oic acid
- Abieta-8(14),9(11),12-triene-18-oic acid
- [1R-(1α,4a
- DEHYDROABIETIC ACID
- Abietic acid, dehydro-
- (-)-Dehydroabietic acid
- 0S5XP6S3AU
- NSC2952
- Isopropyl podoca
- Isopropyl podocarpa-8,11,13-trien-15-oic acid
- MFCD09839012
- HY-N6869
- S3226
- (1R,4aS,10aR)-1,4a-dimethyl-7-(propan-2-yl)-1,2,3,4,4a,9,10,10a-octahydrophenanthrene-1-carboxylic acid
- EINECS 217-102-8
- 1-Phenanthrenecarboxylic acid, 1,2,3,4,4a,9,10,10a-octahydro-1,4a-dimethyl-7-(1-methylethyl)-, (1R-(1alpha,4abeta,10aalpha))-
- rel-(1R,4aS,10aR)-7-Isopropyl-1,4a-dimethyl-1,2,3,4,4a,9,10,10a-octahydrophenanthrene-1-carboxylicacid
- Podocarpa-8,11,13-trien-15-oic acid, 13-isopropyl-
- A881721
- 6980-63-8
- 1-Phenanthrenecarboxylic acid,2,3,4,4a,9,10,10a-octahydro-1,4a-dimethyl-7-(1-methylethyl)-, [1R-(1.alpha.,4a.beta.,10a.alpha.)]-
- 13-Isopropylpodocarpa-8,11,13-trien-15-oic acid
- FT-0633812
- NS00010328
- Dehydroabietic acid, >=95% (LC/MS-ELSD)
- 1-Phenanthrenecarboxylic acid, 1,2,3,4,4a,9,10,10a-octahydro-1,4a-dimethyl-7-(1-methylethyl)-, (1R,4aS,10aR)-
- AC-34629
- 1,3,4,4a,9,10,10a-Octahydro-1,4a-dimethyl-7-(1-methylethyl)-1-phenanthrenecarboxylic acid
- 1740-19-8
- (+)-Dehydroabietic acid, tech grade
- BRN 2059290
- NFWKVWVWBFBAOV-MISYRCLQSA-N
- 5-Podocarpa-8,11,13-trien-15-oic acid, 13-isopropyl-
- UNII-0S5XP6S3AU
- BDBM50143600
- Q27110153
- (1R-(1alpha,4Abeta,10aalpha))-1,2,3,4,4a,9,10,10a-octahydro-7-isopropyl-1,4a-dimethylphenanthren-1-carboxylic acid
- DTXSID8022163
- 1ST40116
- 1-PHENANTHRENECARBOXYLIC ACID, 1,2,3,4,4A,9,10,10A- OCTAHYDRO-1,4A-DIMETHYL-7-(1-METHYLETHYL)-, (1R,4AS,10AR)-
- (1R-(1ALPHA,4ABETA,10AALPHA))-1,2,3,4,4A,9,10,10A-OCTAHYDRO- 7-ISOPROPYL-1,4A-DIMETHYLPHENANTHREN-1-CARBOXYLIC ACID
- NSC-2952
- 1-Phenanthrenecarboxylic acid, 1,2,3,4,4a,9,10,10a-octahydro-1,4a-dimethyl-7-(1-methylethyl)-, [1R-(1,4a,10a)]-
- 13-Isopropylpodocarpa-8,13-trien-15-oic acid
- SCHEMBL222078
- EN300-6730478
- rel-(1R,4aS,10aR)-7-Isopropyl-1,4a-dimethyl-1,2,3,4,4a,9,10,10a-octahydrophenanthrene-1-carboxylic acid
- CHEMBL12850
- AMY22483
- CS-W012130
- LMPR0104050005
- W-107855
- AKOS015917291
- Abieta-8,13-trien-18-oic acid
- InChI=1/C20H28O2/c1-13(2)14-6-8-16-15(12-14)7-9-17-19(16,3)10-5-11-20(17,4)18(21)22/h6,8,12-13,17H,5,7,9-11H2,1-4H3,(H,21,22)/t17-,19-,20-/m1/s
- 4-09-00-02389 (Beilstein Handbook Reference)
- Podocarpa-8,13-trien-15-oic acid, 13-isopropyl-
- CHEBI:29571
- 1-Phenanthrenecarboxylic acid, 1,2,3,4,4a,9,10,10a-octahydro-1,4a-dimethyl-7-(1-methylethyl)-, [1R-(1.alpha.,4a.beta.,10a.alpha.)]-
- 1,2,3,4,4a,9,10,10a-Octahydro-1,4a-dimethyl-7-(1-methylethyl)-1-phenanthrenecarboxylate
- 13-Isopropylpodocarpa-8,11,13-trien-15-Oate
- (-)-Dehydroabietate
- DTXCID402163
- 1,2,3,4,4a,9,10,10a-Octahydro-1,4a-dimethyl-7-(1-methylethyl)-1-phenanthrenecarboxylic acid-, [1R-(1.alpha.,4a.beta.,10a.alpha.)]-
- 1,2,3,4,4a,9,10,10a-Octahydro-1,4a-dimethyl-7-(1-methylethyl)-1-phenanthrenecarboxylic acid-, (1R-(1alpha,4abeta,10aalpha))-
- [1R-(1alpha,4abeta,10aalpha)]-1,2,3,4,4a,9,10,10a-octahydro-7-isopropyl-1,4a-dimethylphenanthren-1-carboxylic acid
- (1R,4aS,10aR)-1,4a-dimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthrene-1-carboxylic acid
- FD20963
- Dehydroabietic acid
- MDL： MFCD09839012
- Inchi： 1S/C20H28O2/c1-13(2)14-6-8-16-15(12-14)7-9-17-19(16,3)10-5-11-20(17,4)18(21)22/h6,8,12-13,17H,5,7,9-11H2,1-4H3,(H,21,22)/t17-,19-,20-/m1/s1
- InChI Key： NFWKVWVWBFBAOV-MISYRCLQSA-N
- SMILES： OC([C@]1(C)CCC[C@]2(C)C3C=CC(C(C)C)=CC=3CC[C@H]21)=O
- BRN： 2059290

Computed Properties

Exact Mass: 300.20900
Monoisotopic Mass: 300.208930132 g/mol
Isotope Atom Count: 0
Hydrogen Bond Donor Count: 1
Hydrogen Bond Acceptor Count: 2
Heavy Atom Count: 22
Rotatable Bond Count: 2
Complexity: 443
Covalently-Bonded Unit Count: 1
Defined Atom Stereocenter Count: 3
Undefined Atom Stereocenter Count : 0
Defined Bond Stereocenter Count: 0
Undefined Bond Stereocenter Count: 0
Surface Charge: 0
XLogP3: 5.6
Topological Polar Surface Area: 37.3
Molecular Weight: 300.4

Experimental Properties

Color/Form: Powder
Density: 1.058
Melting Point: 174-176 oC
Boiling Point: 394.13°C (rough estimate)
Flash Point: 202.5±20.3 °C
Refractive Index: 1.5404 (estimate)
Solubility: 2.20e-05 M
PSA: 37.30000
LogP: 4.90490
Solubility: Soluble in ethanol, benzene, chloroform, ether, acetone, carbon dioxide and dilute sodium hydroxide solution, insoluble in water.

Dehydroabietic acid Security Information

Signal Word：warning
Hazard Statement： H303May be harmful if swallowed+H313Skin contact may be harmful+H333Inhalation may be harmful to the body
Warning Statement： P264Thoroughly clean after treatment
P280Wear protective gloves/Wear protective clothing/Wear protective goggles/Wear a protective mask
P305If it enters the eyes
P351Rinse carefully with water for a few minutes
P338Remove the contact lens(If any)And easy to operate,Continue flushing
P337If eye irritation persists
P313Obtain medical advice/care
Hazardous Material transportation number：UN 2811 6.1 / PGIII
Hazard Category Code： 25-50
Safety Instruction： 45-61
Hazardous Material Identification：
Storage Condition：Please store the product under the recommended condition sin the description

Dehydroabietic acid Pricemore >>

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Dehydroabietic acid Suppliers

Amadis Chemical Company Limited

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(CAS:1740-19-8)Dehydroabietic acid

Order Number:A881721

Stock Status:in Stock

Quantity:10mg/100g

Purity:99%

Pricing Information Last Updated:Friday, 30 August 2024 11:04

Price ($):184.0/435.0

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Product Official Link

Tiancheng Chemical (Jiangsu) Co., Ltd

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Audited Supplier

(CAS:1740-19-8)Dehydroabietlc acid

Order Number:LE10276;LE26512588;LE3813

Stock Status:in Stock

Quantity:25KG,200KG,1000KG

Purity:99%

Pricing Information Last Updated:Friday, 20 June 2025 12:03

Price ($):discuss personally

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Dehydroabietic acid Related Literature

1. Synthesis and biological evaluation of 2-aryl-benzimidazole derivatives of dehydroabietic acid as novel tubulin polymerization inhibitors

Ting-Ting Miao,Xu-Bing Tao,Dong-Dong Li,Hao Chen,Xiao-Yan Jin,Yi Geng,Shi-Fa Wang,Wen Gu RSC Adv. 2018 8 17511
2. Ni2(R*COO)4(H2O)(4,4′-bipy)2—a robust homochiral quartz-like network with large chiral channels

Zhen-Feng Chen,Shu-Feng Zhang,Hai-Sheng Luo,Brendan F. Abrahams,Hong Liang CrystEngComm 2007 9 27
3. Synthesis and structural characterisation of ring B oxidised derivatives of dehydroabietic acid

Silvia M. C. S. Monteiro,Armando J. D. Silvestre,Artur M. S. Silva,José A. S. Cavaleiro,Vitor Félix,Michael G. B. Drew New J. Chem. 2001 25 1091
4. Aromatic abietane diterpenoids: their biological activity and synthesis

Miguel A. González Nat. Prod. Rep. 2015 32 684
5. Biotransformation of diterpenes

María Rico-Martínez,Fernanda G. Medina,Joaquín G. Marrero,Soraya Osegueda-Robles RSC Adv. 2014 4 10627

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