D(+)-Camphor - ≥96% , CAS No.464-49-3

Name: D(+)-Camphor - ≥96% , CAS No.464-49-3
SKU: C106734
Availability: InStock

CAS: 464-49-3 Cat. No.: C106734 Summenformel: C₁₀H₁₆O Molekulargewicht: 152.23 Beilstein Registry Number: 2042745 EG-Nummer: 207-355-2

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GRADE & PURITY ≥96%

Synonyms

Storage

Room temperature

Shipped In

Normal

Übersicht Specifications Namen und Kennungen Documentation Advanced Data Taxonomic Classification 3D-Struktur Zugehörige Ziele (menschlich) Zugehörige Ziele (nicht menschlich) Wirkungsmechanismen Zertifikate (CoA, COO, BSE/TSE und Analyse-Diagramm) Chemische und physikalische Eigenschaften FAQs und Artikel Citations of This Product Referenzen Lösungsrechner Bewertungen

🧪

Why this grade

≥96% 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.

📚

Literature proof

Cited in 8 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Übersicht

Chiral intermediate and auxiliary

Specifications

Synonyme

Spezifikationen & Reinheit

≥96%

Storage

Room temperature

Verschickt in

Normal

Aktionsart

INHIBITOR

Reinheit

≥96%

Namen und Kennungen

Pubchem Sid	504757435
Pubchem Sid Url	https://pubchem.ncbi.nlm.nih.gov/substance/504757435
Kanonisches Lächeln	CC1(C2CCC1(C(=O)C2)C)C
IUPAC Name	(1R,4R)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-one
InChIKey	DSSYKIVIOFKYAU-XCBNKYQSSA-N
INCHI	1S/C10H16O/c1-9(2)7-4-5-10(9,3)8(11)6-7/h7H,4-6H2,1-3H3/t7-,10+/m1/s1
Isomere SMILES	C[C@@]12CC[C@@H](C1(C)C)CC2=O
WGK Deutschland	1
RTECS	EX1260000
UN-Nummer	2717
Verpackungsgruppe	III
Molekulargewicht	152.23
Beilstein	2042745
Reaxy-Rn	1907611
Reaxys-RN_link_address	https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1907611&ln=

Documentation

📋 Safety Data Sheet (SDS)

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

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✅ Certificate of Analysis (COA)

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

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📊 Datasheet

Quick-reference summary of product specifications and applications.

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🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

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Advanced Data

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Lipids and lipid-like molecules
  - Klasse Prenol lipids
    - Subclass Monoterpenoids

Kingdom	Organic compounds
Superclass	Lipids and lipid-like molecules
Klasse	Prenol lipids
Subclass	Monoterpenoids
Intermediate Tree Nodes	Not available
Direct Parent	Bicyclic monoterpenoids
Alternative Parents	Ketones Organic oxides Hydrocarbon derivatives
Molecular Framework	Aliphatic homopolycyclic compounds
Substituents	Bicyclic monoterpenoid - Bornane monoterpenoid - Ketone - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aliphatic homopolycyclic compound
Beschreibung	This compound belongs to the class of organic compounds known as bicyclic monoterpenoids. These are monoterpenoids containing exactly 2 rings, which are fused to each other.
External Descriptors	camphor
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61. DOI: 10.1186/s13321-016-0174-y

3D-Struktur

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PDE5A Tclin Phosphodiesterase 5A (5113 Activities)

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EGFR Tclin Epidermal growth factor receptor erbB1 (33727 Activities)

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CA2 Tclin Carbonic anhydrase II (17698 Activities)

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ESR1 Tclin Estrogen receptor alpha (17718 Activities)

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HMGCR Tclin HMG-CoA reductase (2475 Activities)

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NR3C1 Tclin Glucocorticoid receptor (14987 Activities)

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INSR Tclin Insulin receptor (5558 Activities)

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PGR Tclin Progesterone receptor (8562 Activities)

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ADRB2 Tclin Beta-2 adrenergic receptor (11824 Activities)

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CHRM2 Tclin Muscarinic acetylcholine receptor M2 (10671 Activities)

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ADRB1 Tclin Beta-1 adrenergic receptor (6630 Activities)

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HTR1A Tclin Serotonin 1a (5-HT1a) receptor (14969 Activities)

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ADRA2A Tclin Alpha-2a adrenergic receptor (9450 Activities)

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AR Tclin Androgen Receptor (11781 Activities)

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CHRM1 Tclin Muscarinic acetylcholine receptor M1 (12690 Activities)

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ACE Tclin Angiotensin-converting enzyme (1423 Activities)

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DRD2 Tclin Dopamine D2 receptor (23596 Activities)

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MAOA Tclin Monoamine oxidase A (11911 Activities)

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CNR1 Tclin Cannabinoid CB1 receptor (20913 Activities)

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DRD1 Tclin Dopamine D1 receptor (9720 Activities)

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DRD4 Tchem Dopamine D4 receptor (7907 Activities)

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ACHE Tclin Acetylcholinesterase (18204 Activities)

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PTGS1 Tclin Cyclooxygenase-1 (9233 Activities)

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SLC6A2 Tclin Norepinephrine transporter (10102 Activities)

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HRH2 Tclin Histamine H2 receptor (5428 Activities)

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ADRA1D Tclin Alpha-1d adrenergic receptor (4171 Activities)

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HTR1B Tclin Serotonin 1b (5-HT1b) receptor (2801 Activities)

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HTR2A Tclin Serotonin 2a (5-HT2a) receptor (14758 Activities)

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HTR2C Tclin Serotonin 2c (5-HT2c) receptor (11471 Activities)

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ADORA1 Tclin Adenosine A1 receptor (17603 Activities)

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CALCR Tclin Calcitonin receptor (2215 Activities)

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SLC6A4 Tclin Serotonin transporter (12625 Activities)

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ADRA1A Tclin Alpha-1a adrenergic receptor (8359 Activities)

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PTGS2 Tclin Cyclooxygenase-2 (13999 Activities)

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HRH1 Tclin Histamine H1 receptor (7573 Activities)

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ADRA1B Tclin Alpha-1b adrenergic receptor (2912 Activities)

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OPRM1 Tclin Mu opioid receptor (19785 Activities)

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DRD3 Tclin Dopamine D3 receptor (14368 Activities)

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AVPR1A Tclin Vasopressin V1a receptor (5412 Activities)

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OPRD1 Tclin Delta opioid receptor (15096 Activities)

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OPRK1 Tclin Kappa opioid receptor (16155 Activities)

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SLC6A3 Tclin Dopamine transporter (10535 Activities)

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KCNH2 Tclin HERG (29587 Activities)

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HTR4 Tclin Serotonin 4 (5-HT4) receptor (2068 Activities)

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ESR2 Tclin Estrogen receptor beta (9272 Activities)

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CYSLTR1 Tclin Cysteinyl leukotriene receptor 1 (2118 Activities)

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ERBB2 Tclin Receptor protein-tyrosine kinase erbB-2 (7851 Activities)

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CHRM4 Tclin Muscarinic acetylcholine receptor M4 (6041 Activities)

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CHRM5 Tclin Muscarinic acetylcholine receptor M5 (4677 Activities)

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ADRA2B Tclin Alpha-2b adrenergic receptor (4412 Activities)

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Agtr2 Angiotensin II type 2 (AT-2) receptor (803 Activities)

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Mc4r Melanocortin receptor 4 (1205 Activities)

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Ltc4s Leukotriene C4 synthase (1 Activities)

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Sigmar1 Sigma opioid receptor (160 Activities)

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Npy1r Neuropeptide Y receptor type 1 (8 Activities)

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Cckar Cholecystokinin A receptor (90 Activities)

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Nos2 Nitric oxide synthase, inducible (3573 Activities)

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Mapk1 MAP kinase ERK2 (650 Activities)

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Hdac6 Histone deacetylase 6 (222 Activities)

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Mmp9 Matrix metalloproteinase 9 (38 Activities)

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Pseudomonas aeruginosa (123386 Activities)

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Staphylococcus aureus (210822 Activities)

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Staphylococcus epidermidis (22802 Activities)

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Escherichia coli (133304 Activities)

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Cutibacterium acnes (887 Activities)

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Candida albicans (78123 Activities)

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Spodoptera littoralis (798 Activities)

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Cavia porcellus (23802 Activities)

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Musca domestica (713 Activities)

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Mus musculus (284745 Activities)

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Influenza A virus (11224 Activities)

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Myzus persicae (1112 Activities)

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Botrytis cinerea (4183 Activities)

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MDCK (10148 Activities)

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Rdl GABA receptor subunit (76 Activities)

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rep Replicase polyprotein 1ab (378 Activities)

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Trpa1 Transient receptor potential cation channel subfamily A member 1 (1003 Activities)

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Colletotrichum fragariae (147 Activities)

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Colletotrichum gloeosporioides (560 Activities)

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Fusarium culmorum (260 Activities)

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Fusarium oxysporum f. sp. lycopersici (29 Activities)

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Leptinotarsa decemlineata (1161 Activities)

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Rhizoctonia solani (2251 Activities)

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Rorc Nuclear receptor ROR-gamma (89407 Activities)

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Fusarium graminearum (1554 Activities)

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Colletotrichum acutatum (300 Activities)

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Corticium (78 Activities)

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Theba pisana (23 Activities)

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Pythium (470 Activities)

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Glra2 Glycine receptor (1745 Activities)

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Wirkungsmechanismen

Zertifikate (CoA, COO, BSE/TSE und Analyse-Diagramm)

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.

17 results found

Lot Number	Certificate Type	Datum	Artikel
D2607221	Certificate of Analysis	Mar 13, 2026	C106734
D2607222	Certificate of Analysis	Mar 13, 2026	C106734
D2607224	Certificate of Analysis	Mar 13, 2026	C106734
D2607239	Certificate of Analysis	Mar 13, 2026	C106734
E2625031	Certificate of Analysis	Mar 13, 2026	C106734
A2203112	Certificate of Analysis	Oct 13, 2025	C106734
A2203104	Certificate of Analysis	Oct 13, 2025	C106734
K2405431	Certificate of Analysis	Oct 28, 2024	C106734
K2405430	Certificate of Analysis	Oct 28, 2024	C106734
K2405428	Certificate of Analysis	Oct 28, 2024	C106734
K2405429	Certificate of Analysis	Oct 28, 2024	C106734
J2415364	Certificate of Analysis	Jun 29, 2024	C106734
J2415365	Certificate of Analysis	Jun 29, 2024	C106734
L1525026	Certificate of Analysis	Aug 04, 2023	C106734
J2418162	Certificate of Analysis	Dec 06, 2021	C106734
J2326106	Certificate of Analysis	Dec 06, 2021	C106734
E2431025	Certificate of Analysis	Dec 06, 2021	C106734

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Chemische und physikalische Eigenschaften

Löslichkeit	Soluble in ethanol (5%),
Spezifische Drehung [α]	44.5 ° (C=20, EtOH)
Flammpunkt (°F)	64℃
Flammpunkt (°C)	64℃
Siedepunkt (°C)	204°C
Schmelzpunkt (°C)	176-180°C
Molekulargewicht	152.230 g/mol
XLogP3	2.200
Hydrogen Bond Donor Count	0
Hydrogen Bond Acceptor Count	1
Rotatable Bond Count	0
Exact Mass	152.12 Da
Monoisotopic Mass	152.12 Da
Topological Polar Surface Area	17.100 Å²
Heavy Atom Count	11
Formal Charge	0
Complexity	217.000
Isotope Atom Count	0
Defined Atom Stereocenter Count	2
Undefined Atom Stereocenter Count	0
Defined Bond Stereocenter Count	0
Undefined Bond Stereocenter Count	0
The total count of all stereochemical bonds	0
Covalently-Bonded Unit Count	1

FAQs und Artikel

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Citations of This Product

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Referenzen

1. Qiao Heng, Zhu Han, Li Hui, Chen Hongjian, Li Shouyin, Chen Cong, Hao Dejun. (2023) Isolation and characterization of gut bacteria associated with the degradation of host-specific terpenoids in Pagiophloeus tsushimanus (Coleoptera: Curculionidae) larvae. JOURNAL OF INSECT SCIENCE, 23 (2): [PMID:37074003] [10.1093/jisesa/iead019]
2. Xing Huang, Linjie Du, Tiantian Liu, Rui Ma, Xing Liu, Haibin Yuan, Shuai Liu. (2022) Insecticidal Activity of a Component, (-)-4-Terpineol, Isolated from the Essential Oil of Artemisia lavandulaefolia DC. against Plutella xylostella (L.). Insects, 13 (12): (1126). [PMID:36555036] [10.3390/insects13121126]
3. Yazhou Shao, Anqi Ning, Yue An, Zhibo Hou, Feng Zhou, Chuyu He, Ji Zhang, Junyu Liang. (2021) Evaluation of the composition and fumigant toxicity against Plodia interpunctella of essential oils from Ajania potaninii and Ajania fruticulosa. JOURNAL OF ASIA-PACIFIC ENTOMOLOGY, [PMID:] [10.1016/j.aspen.2021.08.012]
4. Bananakere Nanjegowda Chandrashekar, Nianduo Cai, Louis W.Y. Liu, Ankanahalli Shankaregowda Smitha, Zefei Wu, Pengcheng Chen, Run Shi, Weijun Wang, Jingwei Wang, Chunmei Tang, Chun Cheng. (2019) Oil boundary approach for sublimation enabled camphor mediated graphene transfer. JOURNAL OF COLLOID AND INTERFACE SCIENCE, [PMID:30901688] [10.1016/j.jcis.2019.03.053]
5. Du Jing, Li Xiao-Yu, Hu He, Xu Li, Yang Shi-Ping, Li Feng-Hua. (2018) Preparation and Imaging Investigation of Dual-targeted C3F8-filled PLGA Nanobubbles as a Novel Ultrasound Contrast Agent for Breast Cancer. Scientific Reports, 8 (1): (1-18). [PMID:29497045] [10.1038/s41598-018-21502-x]
6. Chang Hui, Kang Wenjia, Zhao Xinyu, Chang Shuai, Li Xinping, Luo Yuxia, Xiong Chuanyin, Zhu Xunjin, Zhang Zhao. (2025) Nanocellulose chiral synergistic effect enhances circularly polarized luminescence of lanthanide electric dipole transition bands. CELLULOSE, [PMID:] [10.1007/s10570-025-06473-3]
7. Li Xu, Caifeng Wan, Jing Du, Hongli Li, Xuesong Liu, Hong Yang, Fenghua Li. (2017) Synthesis, characterization, and in vitro evaluation of targeted gold nanoshelled poly(d,l-lactide-co-glycolide) nanoparticles carrying anti p53 antibody as a theranostic agent for ultrasound contrast imaging and photothermal therapy. JOURNAL OF BIOMATERIALS SCIENCE-POLYMER EDITION, [PMID:28044473] [10.1080/09205063.2016.1277828]
8. Cui-Wei Wang, Shi-Ping Yang, He Hu, Jing Du, Feng-Hua Li. (2014) Synthesis, characterization and in vitro and in vivo investigation of C3F8-filled poly(lactic-co-glycolic acid) nanoparticles as an ultrasound contrast agent. Molecular Medicine Reports, 11 (3): (1885-1890). [PMID:25394467] [10.3892/mmr.2014.2938]

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D(+)-Camphor - ≥96% , CAS No.464-49-3

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D(+)-Camphor - ≥96% , CAS No.464-49-3

Why this grade

Storage & shipping

Quality documents

Literature proof

Übersicht

Specifications

Documentation

📋 Safety Data Sheet (SDS)

✅ Certificate of Analysis (COA)

📊 Datasheet

🔬 Specification Sheet

Advanced Data

Show more ⌵

Molarity Calculator

Dilution Calculator

Reconstitution Calculator

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