Emamectin-benzoate - analytical standard, ≥95% , CAS No.155569-91-8

CAS: 155569-91-8 Cat. No.: E110058 Peso molecular: 1008.24 Número EC: 605-015-1
Disponible para pedir
GRADE & PURITY Analytical standard ? Analytical standard — certified-purity material for quantitative calibration. Use to prepare calibration standards and validate analytical methods. ≥95%
Synonyms
(4/'/'R)-4/'/'-DEOXY-4/'/'-(METHYLAMINO)AVERMECTIN B1 BENZOATE | SCHEMBL4291571 | Emamectin Benzoate, 90% | AKOS025311598 | MK-244MK-244 | 1ST25001 | MK-244 | AS-72351 | Emamectin | S4423 | Emamectin benzoate
Storage
Room temperature
Shipped In
Normal
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
100mg
E110058-100mg
5

105,90US$

123,90US$
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Why this grade

analytical standard, ≥95% Analytical standard for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

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

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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 11 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Descripción general

An insecticidal heterocyclic reagent

Specifications

Sinónimos
(4/'/'R)-4/'/'-DEOXY-4/'/'-(METHYLAMINO)AVERMECTIN B1 BENZOATE | SCHEMBL4291571 | Emamectin Benzoate, 90% | AKOS025311598 | MK-244MK-244 | 1ST25001 | MK-244 | AS-72351 | Emamectin | S4423 | Emamectin benzoate
Especificaciones y pureza
analytical standard, ≥95%
Condiciones de almacenamiento de almacenamiento
Room temperature
Enviado en
Normal
Grado
Analytical standard
Pureza
≥95%
Nombres e identificadores
Sonrisas canónicasCCC(C)C1C(C=CC2(O1)CC3CC(O2)CC=C(C(C(C=CC=C4COC5C4(C(C=C(C5O)C)C(=O)O3)O)C)OC6CC(C(C(O6)C)OC7CC(C(C(O7)C)NC)OC)OC)C)C.C1=CC=C(C=C1)C(=O)O
IUPAC Namebenzoic acid;(1'R,2R,3S,4'S,6S,8'R,10'E,12'S,13'S,14'E,16'E,20'R,21'R,24'S)-2-[(2S)-butan-2-yl]-21',24'-dihydroxy-12'-[(2R,4S,5S,6S)-4-methoxy-5-[(2S,4S,5S,6S)-4-methoxy-6-methyl-5-(methylamino)oxan-2-yl]oxy-6-methyloxan-2-yl]oxy-3,11',13',22'-tetramethylspiro[2,3-dihydropyran-6,6'-3,7,19-trioxatetracyclo[15.6.1.14,8.020,24]pentacosa-10,14,16,22-tetraene]-2'-one
InChIKeyGCKZANITAMOIAR-XWVCPFKXSA-N
INCHI1S/C49H75NO13.C7H6O2/c1-12-26(2)44-29(5)18-19-48(63-44)24-35-21-34(62-48)17-16-28(4)43(27(3)14-13-15-33-25-56-46-42(51)30(6)20-36(47(52)59-35)49(33,46)53)60-40-23-38(55-11)45(32(8)58-40)61-39-22-37(54-10)41(50-9)31(7)57-39;8-7(9)6-4-2-1-3-5-6/h13-16,18-20,26-27,29,31-32,34-46,50-51,53H,12,17,21-25H2,1-11H3;1-5H,(H,8,9)/b14-13+,28-16+,33-15+;/t26-,27-,29-,31-,32-,34+,35-,36-,37-,38-,39-,40-,41-,42+,43-,44+,45-,46+,48+,49+;/m0./s1
Isómeros SMILES CC[C@H](C)[C@@H]1[C@H](C=C[C@@]2(O1)C[C@@H]3C[C@H](O2)C/C=C(/[C@H]([C@H](/C=C/C=C/4\CO[C@H]5[C@@]4([C@@H](C=C([C@H]5O)C)C(=O)O3)O)C)O[C@H]6C[C@@H]([C@H]([C@@H](O6)C)O[C@H]7C[C@@H]([C@H]([C@@H](O7)C)NC)OC)OC)\C)C.C1=CC=C(C=C1)C(=O)O
WGK Alemania 3
RTECS CL1203005
CAS alternativo 137512-74-4
Número ONU 2811
Grupo de embalaje III
Peso molecular 1008.24
Reaxy-Rn 37329556
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=37329556&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.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganic oxygen compounds
ClaseOrganooxygen compounds
SubclassCarbohydrates and carbohydrate conjugates
Intermediate Tree Nodes Aminosaccharides
Direct ParentAminoglycosides
Alternative Parents Macrolides and analogues  O-glycosyl compounds  Benzoic acids  Benzoyl derivatives  Ketals  Pyrans  Oxanes  Monosaccharides  Tetrahydrofurans  Tertiary alcohols  Secondary alcohols  Amino acids and derivatives  Carboxylic acid esters  Lactones  Oxacyclic compounds  Monocarboxylic acids and derivatives  Carboxylic acids  Dialkyl ethers  Dialkylamines  Organic oxides  Carbonyl compounds  Organopnictogen compounds  Hydrocarbon derivatives  
Molecular FrameworkNot available
Substituents Aminoglycoside core - Macrolide - Glycosyl compound - O-glycosyl compound - Benzoic acid or derivatives - Benzoic acid - Benzoyl - Ketal - Benzenoid - Pyran - Oxane - Monocyclic benzene moiety - Monosaccharide - Tetrahydrofuran - Tertiary alcohol - Amino acid or derivatives - Secondary alcohol - Carboxylic acid ester - Lactone - Organoheterocyclic compound - Secondary amine - Oxacycle - Acetal - Carboxylic acid derivative - Monocarboxylic acid or derivatives - Carboxylic acid - Dialkyl ether - Secondary aliphatic amine - Ether - Carbonyl group - Organic nitrogen compound - Organonitrogen compound - Organopnictogen compound - Amine - Alcohol - Organic oxide - Hydrocarbon derivative - Aromatic heteropolycyclic compound
DescripciónThis compound belongs to the class of organic compounds known as aminoglycosides. These are molecules or a portion of a molecule composed of amino-modified sugars.
External Descriptors Not available
Estructura 3D
Modelo de Estructura Química Interactiva





Objetivos asociados (humanos)
ESR1 Tclin Estrogen receptor alpha (17718 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
NR3C1 Tclin Glucocorticoid receptor (14987 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
AR Tclin Androgen Receptor (11781 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
VDR Tclin Vitamin D receptor (26531 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PPARG Tclin Peroxisome proliferator-activated receptor gamma (15191 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
THRB Tclin Thyroid hormone receptor beta-1 (7926 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
RXRA Tclin Retinoid X receptor alpha (3637 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
NR1H4 Tclin Bile acid receptor FXR (6228 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
NFKB1 Tclin Nuclear factor NF-kappa-B p105 subunit (1459 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
TP53 Tchem Cellular tumor antigen p53 (48468 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Objetivos asociados (no humanos)
Ppard Peroxisome proliferator-activated receptor delta (358 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Nfe2l2 Nuclear factor erythroid 2-related factor 2 (214 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mecanismos de acción
Certificados (CoA, COO, BSE/TSE y tabla de análisis)
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.

1 results found

Lot NumberCertificate TypeFechaArticulo
H2119010Certificate of AnalysisMay 11, 2023 E110058
Propiedades químicas y físicas
Punto de fusión (°C)141-146°C
Peso molecular1008.200 g/mol
XLogP3
Hydrogen Bond Donor Count4
Hydrogen Bond Acceptor Count16
Rotatable Bond Count10
Exact Mass1007.56 Da
Monoisotopic Mass1007.56 Da
Topological Polar Surface Area199.000 Ų
Heavy Atom Count72
Formal Charge0
Complexity1850.000
Isotope Atom Count0
Defined Atom Stereocenter Count20
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count3
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds3
Covalently-Bonded Unit Count2
Citations of This Product
Referencias
1. Bin Jiao, Huimin Ye, Xinwei Liu, Jiexun Bu, Junhan Wu, Wenpeng Zhang, Yunfeng Zhang, Zheng Ouyang.  (2021)  Handheld Mass Spectrometer with Intelligent Adaptability for On-Site and Point-of-Care Analysis.  ANALYTICAL CHEMISTRY,      [PMID:34780167] [10.1021/acs.analchem.1c02508]
2. Yifan Li, Hong Sun, Hassan Yasoob, Zhen Tian, Yue Li, Ruichi Li, Shengli Zheng, Jiyuan Liu, Yalin Zhang.  (2021)  Biogenetic cantharidin is a promising leading compound to manage insecticide resistance of Mythimna separata (Lepidoptera: Noctuidae).  PESTICIDE BIOCHEMISTRY AND PHYSIOLOGY,      [PMID:33518040] [10.1016/j.pestbp.2020.104769]
3. Zhi Liang, Xi Zhou, Yinlong Li, Min Zhou, Xutao Yang, Shengnan Zhang, Jacob D. Wickham, Qing-He Zhang, Longwa Zhang.  (2024)  Distribution, Residue Dynamics, and Insecticidal Efficacy of Trunk-Injected Emamectin Benzoate in Pecan Trees.  Forests,  15  (3): (535).  [PMID:] [10.3390/f15030535]
4. Wenying Sun, Jing Liu, Xu Shi, Yanju Bi, Huanyi Liu, Tong Xu.  (2025)  Emamectin Benzoate and Microplastics Led to Skeletal Muscle Atrophy in Common Carp via Induced Oxidative Stress, Mitochondrial Dysfunction, and Protein Synthesis and Degradation Imbalance.  JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY,      [PMID:39840891] [10.1021/acs.jafc.4c10479]
5. Lu Li, Wan Li, Yufeng Liu, Bing Han, Yanbo Yu, Hongjin Lin.  (2024)  Emamectin benzoate exposure induced carp kidney injury by triggering mitochondrial oxidative stress to accelerate ferroptosis and autophagy.  PESTICIDE BIOCHEMISTRY AND PHYSIOLOGY,      [PMID:39084778] [10.1016/j.pestbp.2024.106017]
6. Jiawen Ji, Siyue Zhu, Xinping Hu, Jianhui Zhu, Sen Pang, Yongqiang Ma, Xuefeng Li.  (2025)  Enhanced residual risk of abamectin induced by 6PPD: in water, soil, and vegetables.  Environmental Science-Processes & Impacts,      [PMID:40099488] [10.1039/D5EM00053J]
7. Hao Wu, Tong Xu, Naixi Yang, Shiwen Xu.  (2025)  Polystyrene-microplastics and Emamectin Benzoate co-exposure induced lipid remodeling by suppressing PPARα signals to drive ACSL4-dependent ferroptosis and carp splenic injury.  PESTICIDE BIOCHEMISTRY AND PHYSIOLOGY,      [PMID:40262874] [10.1016/j.pestbp.2025.106396]
8. Xinda Lin, Yiwen Mao, Ling Zhang.  (2018)  Binding properties of four antennae-expressed chemosensory proteins (CSPs) with insecticides indicates the adaption of Spodoptera litura to environment.  PESTICIDE BIOCHEMISTRY AND PHYSIOLOGY,      [PMID:29626991] [10.1016/j.pestbp.2018.02.011]
9. Hui Pan, Meng Jin, Fang Zhang, Xuelei Chen, Mengping Zhang, Haiyan Wei, Xiao Meng, Wenwen Chen, Zhihu Zhang, Cuijuan Wang.  (2025)  Point-of-use SERS approach for efficient detecting chlorfenapyr and emamectin benzoate residues based on au trisoctahedrons@metal−organic framework modified on polya-mide 6 films.  FOOD CHEMISTRY,      [PMID:40279892] [10.1016/j.foodchem.2025.144366]
10. Panpan Ma, Haiyuan Zhang, Mingyu Cui, Yuqi Zhang, Zhongyu Cai.  (2025)  Two-dimensional photonic hydrogel aptasensors for selective detection of pesticide carbendazim.  MICROCHEMICAL JOURNAL,      [PMID:] [10.1016/j.microc.2025.115970]
11. Tang Rui, Wei Dandan, Luo Chun-Hua, Qin Juan-Rong, Mobarak Syed-Husne, Yu Xing-Lin, Liu Tong-Xian.  (2025)  High-temperature acclimation during development modulates efficacy of emamectin benzoate against Mythimna separata (Lepidoptera: Noctuidae).  JOURNAL OF ECONOMIC ENTOMOLOGY,      [PMID:41092431] [10.1093/jee/toaf277]
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