(-)-Ambroxide - ≥98%(GC) , CAS No.6790-58-5

CAS: 6790-58-5 Cat. No.: A151758 Molecular Weight: 236.4 EC Number: 229-861-2
AVAILABLE TO ORDER
GRADE & PURITY ≥98%(GC)
Synonyms
(-)-Ambroxide, >=99% | AMBROFIX | YPZUZOLGGMJZJO-LQKXBSAESA-N | Naphtho(2,1-b)furan, dodecahydro-3a,6,6,9a-tetramethyl-, (3aR,5aS,9aS,9bR)- | (-)-ambrox | ?3,5,5-TRIMETHYLCYCLOHEXANE-1,2-DIONE | DTXSID0047113 | TD34B3O8M9 | UNII-K60YJF1E9A | 1,5,5,9-Tetra
Storage
Room temperature
Shipped In
Normal
 ·  off list, applied to all prices below.
Size
Status
Price
Qty
1g
A151758-1g
1

$9.90

$14.90
Save $5.00 (33.56%)
5g
A151758-5g
4

$35.90

$53.90
Save $18.00 (33.40%)
25g
A151758-25g
3

$119.90

$179.90
Save $60.00 (33.35%)
100g
A151758-100g
2

$383.90

$575.90
Save $192.00 (33.34%)
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Why this grade

≥98%(GC) for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Room temperature Ships Normal Check lot-specific COA for exact specifications.

📋

Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

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Literature proof

Cited in 9 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Overview

Product Application:

(-)-Ambroxide is one of the most important components of natural Ambergris and is useful for making amber fragrance. 

Specifications

Synonyms
(-)-Ambroxide, >=99% | AMBROFIX | YPZUZOLGGMJZJO-LQKXBSAESA-N | Naphtho(2, 1-b)furan, dodecahydro-3a, 6, 6, 9a-tetramethyl-, (3aR, 5aS, 9aS, 9bR)- | (-)-ambrox | ?3, 5, 5-TRIMETHYLCYCLOHEXANE-1, 2-DIONE | DTXSID0047113 | TD34B3O8M9 | UNII-K60YJF1E9A | 1, 5, 5, 9-Tetra
Specifications & Purity
≥98%(GC)
Storage
Room temperature
Shipped In
Normal
Purity
≥98%(GC)
Names and Identifiers
Pubchem Sid488196864
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488196864
Canonical SmilesCC1(CCCC2(C1CCC3(C2CCO3)C)C)C
IUPAC Name(3aR,5aS,9aS,9bR)-3a,6,6,9a-tetramethyl-2,4,5,5a,7,8,9,9b-octahydro-1H-benzo[e][1]benzofuran
InChIKeyYPZUZOLGGMJZJO-LQKXBSAESA-N
INCHI1S/C16H28O/c1-14(2)8-5-9-15(3)12(14)6-10-16(4)13(15)7-11-17-16/h12-13H,5-11H2,1-4H3/t12-,13+,15-,16+/m0/s1
Isomeric SMILES C[C@]12CCCC([C@@H]1CC[C@@]3([C@@H]2CCO3)C)(C)C
WGK Germany 1
Molecular Weight 236.4
Reaxy-Rn 117672
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=117672&ln=

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganoheterocyclic compounds
ClassNaphthofurans
SubclassNot available
Intermediate Tree Nodes Not available
Direct ParentNaphthofurans
Alternative Parents Tetrahydrofurans  Oxacyclic compounds  Dialkyl ethers  Hydrocarbon derivatives  
Molecular FrameworkAliphatic heteropolycyclic compounds
Substituents Naphthofuran - Tetrahydrofuran - Oxacycle - Ether - Dialkyl ether - Organic oxygen compound - Hydrocarbon derivative - Organooxygen compound - Aliphatic heteropolycyclic compound
DescriptionThis compound belongs to the class of organic compounds known as naphthofurans. These are compounds containing a furan ring fused to a naphthalene moiety. Furan is a 5 membered- ring aromatic ring with four carbon and one oxygen atoms. Naphthalene is a polycyclic aromatic hydrocarbon made up of two fused benzene rings.
External Descriptors organic heterotricyclic compound - diterpenoid
3D Structure
Interactive Chemical Structure Model





Mechanisms of Action
Certificates(CoA,COO,BSE/TSE and Analysis Chart)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

9 results found

Lot NumberCertificate TypeDateItem
C2219071Certificate of AnalysisJan 19, 2026 A151758
C2219093Certificate of AnalysisJan 19, 2026 A151758
C2219107Certificate of AnalysisJan 19, 2026 A151758
C1814146Certificate of AnalysisOct 14, 2025 A151758
J2530204Certificate of AnalysisJul 04, 2024 A151758
J2530220Certificate of AnalysisJul 04, 2024 A151758
C2308567Certificate of AnalysisFeb 14, 2022 A151758
E2320312Certificate of AnalysisJan 19, 2022 A151758
C1814144Certificate of AnalysisJan 19, 2022 A151758
Chemical and Physical Properties
Specific Rotation[α]-25° (C=1,CHCl3)
Melt Point(°C)77 °C
Molecular Weight236.390 g/mol
XLogP34.700
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count1
Rotatable Bond Count0
Exact Mass236.214 Da
Monoisotopic Mass236.214 Da
Topological Polar Surface Area9.200 Ų
Heavy Atom Count17
Formal Charge0
Complexity321.000
Isotope Atom Count0
Defined Atom Stereocenter Count4
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Documents & Articles
Citations of This Product
References
1. Tianyu Chen, Jing Yao, Keao Quan, Jingchen Xu, Xudong Hang, Qian Tong, Genyan Liu, Peipei Luo, Liping Zeng, Ganzhu Feng, Hongkai Bi.  (2023)  Repurposing a human acetyl-CoA carboxylase inhibitor firsocostat to treat fungal candidiasis alone and in combination.  ANTIMICROBIAL AGENTS AND CHEMOTHERAPY,      [PMID:38018962] [10.1128/aac.01131-23]
2. Zhiwei Huang, Hongsheng Dai, Xiaoyu Zhang, Qiao Wang, Jing Sun, Yunxia Deng, Ping Shi.  (2021)  BSC2 induces multidrug resistance via contributing to the formation of biofilm in Saccharomyces cerevisiae.  CELLULAR MICROBIOLOGY,  23  (12): (e13391).  [PMID:34482605] [10.1111/cmi.13391]
3. Yingying Kong, Qiao Wang, Fangqi Cao, Xiaoyu Zhang, Zhijia Fang, Ping Shi, Handong Wang, Yuhu Shen, Zhiwei Huang.  (2020)  BSC2 enhances cell resistance to AmB by inhibiting oxidative damage in Saccharomyces cerevisiae.  FREE RADICAL RESEARCH,      [PMID:32295440] [10.1080/10715762.2020.1751151]
4. Chang Shu, Tengfei Li, Wen Yang, Duo Li, Shunli Ji, Li Ding.  (2018)  Amphotericin B-conjugated polypeptide hydrogels as a novel innovative strategy for fungal infections.  Royal Society Open Science,  (3):   [PMID:29657786] [10.1098/rsos.171814]
5. Liting Cheng, Zhongyi Ma, Xinlin Yang, Xue Wang, Yuqiong Wang, Xinlong Liu, Zhongjie Tang, Dingxi Jang, Guojian Liao, Tongbao Liu, Shuang Wu, Chong Li.  (2025)  All-stage targeted therapy for invasive cryptococcosis through interaction between the secretory protein Cig1 and hemin.  Asian Journal of Pharmaceutical Sciences,      [PMID:40777840] [10.1016/j.ajps.2025.101053]
6. Peng Min, Zhang Chen, Duan Yuan-Yuan, Liu Hai-Bo, Peng Xin-Yuan, Wei Qian, Chen Qi-Ying, Sang Hong, Kong Qing-Tao.  (2024)  Antifungal activity of the repurposed drug disulfiram against Cryptococcus neoformans.  Frontiers in Pharmacology,      [PMID:38273827] [10.3389/fphar.2023.1268649]
7. Yunyun Wu, Yanjing Wang, Weili Li, Diyi Li, Panpan Song, Yaqing Kang, Xiaoqing Han, Xinbo Wang, Hongkun Tian, Abdur Rauf, Jiao Yan, Haiyuan Zhang, Xi Li.  (2024)  Construction of piezoelectric, conductive and injectable hydrogels to promote wound healing through electrical stimulation.  Acta Biomaterialia,      [PMID:39577481] [10.1016/j.actbio.2024.11.028]
8. Qi Liu, Tong Luo, Yiyan Yin, Yan Ouyang, Min Xiao, Hongxia Gao, Teerawat Sema, Zhiwu Liang.  (2024)  Oxidative stability of structurally varied amines for post-combustion CO2 capture.  CHEMICAL ENGINEERING SCIENCE,      [PMID:] [10.1016/j.ces.2024.120458]
9. Kaiwen Bao, Yunfan Li, Yantao Li, Shuai Wu, Sheng Ni, Xiong Zhao, Ya Wang, Yi Liang, Qiao Chen, Xinmei Duan, Da sun, Li Zhu, Wei Wu.  (2025)  Macrophage membrane-camouflaged dual drug-based biomimetic pH-responsive nanomedicine for synergistic antifungal-antioxidant therapy in oral candidiasis.  Acta Biomaterialia,      [PMID:40935301] [10.1016/j.actbio.2025.09.003]
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