Abietic acid
technical, ~75% (GC)
Manufacturer: Sigma Aldrich
CAS Number: 514-10-3
Synonym(S): 7,13-abietadien-18-oic acid, Abietate, L-Abietic acid, Rosin acid, Sylvic acid, sylvic acid
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| 25 G | 00010-25-G | In Stock | ₹ 9,558.48 |
| 100 G | 00010-100-G | In Stock | ₹ 17,514.85 |
00010 - 25 G
In Stock
Quantity
1
Base Price: ₹ 9,558.48
GST (18%): ₹ 1,720.526
Total Price: ₹ 11,279.006
grade
technical
Quality Level
100
Assay
~75% (GC)
form
solid
optical activity
[α]20/D −85±10°, c = 1% in ethanol
mp
139-142 °C (lit.)150-165 °C
storage temp.
2-8°C
SMILES string
CC(C)C1=CC2=CC[C@@H]3[C@](C)(CCC[C@@]3(C)C(O)=O)[C@H]2CC1
InChI
1S/C20H30O2/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/h7,12-13,16-17H,5-6,8-11H2,1-4H3,(H,21,22)/t16-,17+,19+,20+/m0/s1
InChI key
RSWGJHLUYNHPMX-ONCXSQPRSA-N
Other Options
| Image | Product Name | Manufacturer | Price Range | |
|---|---|---|---|---|
 | eMolecules Medchem Express / Abietic acid / 5mg / 495800989 / HY-N6871 / / 514-10-3 / [null] / 302.458 / C20H30O2 | eMolecules | ₹ 6,297.22 | |
 | Medchemexpress LLC HY-N6871 5mg Medchemexpress, Abietic acid CAS:514-10-3 Purity:>98% | Medchemexpress LLC | ₹ 4,491.90 | |
 | Sigma Aldrich Fine Chemicals Biosciences Abietic acid technical, ~75% (GC) | 514-10-3 | MFCD03423567 | 100G | Sigma Aldrich Fine Chemicals Biosciences | ₹ 18,446.74 | |
 | Sigma Aldrich Fine Chemicals Biosciences Abietic acid technical, ~75% (GC) | 514-10-3 | MFCD03423567 | 25G | Sigma Aldrich Fine Chemicals Biosciences | ₹ 10,586.34 | |
 | Abietic acid | ChemScene | ₹ 3,336.84 - ₹ 10,096.08 | |
 | 514-10-3 | (1R,4aR,4bR,10aR)-1,2,3,4,4a,4b,5,6,10,10a-Decahydro-1,4a-dimethyl-7-(1-methylethyl)-1-phenanthrenecarboxylic acid | A2B Chem | ₹ 1,796.76 - ₹ 46,801.32 |
Related Products
Description
- Application: Abietic acid can be used as a precursor in the preparation of: Epoxy and petrochemical curing agents.[1][2] Dehydroabietic acid derivatives as potential antitumor, antimycotic, and antiviral agents.[3][4]It can also be used as a starting material in the total synthesis of: (−)-triptonide and (−)-triptolide as potent antitumor and immunosuppressant agents[5] quinone (−)-12-deoxyroyleanone as antileishmanial agent[5] abietic acid-derived catechol (methyl 11,12-dihydroxyabietate-8,11,13-trien-18-oate, MDTO) as a potential antioxidant agent[6]
- Other Notes: Starting material for natural product synthesis[7][8][9]; Epoxidation with MCPBA[10]
SAFETY INFORMATION
Pictograms
Signal Word
Warning
Hazard Statements
Precautionary Statements
P261 - P264 - P271 - P273 - P302 + P352 - P305 + P351 + P338
Hazard Classifications
Aquatic Acute 1 - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Compare Similar Items
Show Difference
grade: technical
Quality Level: 100
Assay: ~75% (GC)
form: solid
optical activity: [α]20/D −85±10°, c = 1% in ethanol
mp: 139-142 °C (lit.)150-165 °C
storage temp.: 2-8°C
SMILES string: CC(C)C1=CC2=CC[C@@H]3[C@](C)(CCC[C@@]3(C)C(O)=O)[C@H]2CC1
InChI: 1S/C20H30O2/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/h7,12-13,16-17H,5-6,8-11H2,1-4H3,(H,21,22)/t16-,17+,19+,20+/m0/s1
InChI key: RSWGJHLUYNHPMX-ONCXSQPRSA-N
grade: __
Quality Level: 100
Assay: ≥97.0% (HPLC)
form: powder or crystals
optical activity: __
mp: 260-265 °C (lit.)
storage temp.: 2-8°C
SMILES string: COc1ccc(cc1)C2=CC(=O)c3c(O)cc(O)cc3O2
InChI: 1S/C16H12O5/c1-20-11-4-2-9(3-5-11)14-8-13(19)16-12(18)6-10(17)7-15(16)21-14/h2-8,17-18H,1H3
InChI key: DANYIYRPLHHOCZ-UHFFFAOYSA-N
grade: primary reference standard
Quality Level: __
Assay: __
form: liquid
optical activity: __
mp: 1-2 °C (lit.)
storage temp.: −20°C
SMILES string: __
InChI: __
InChI key: __