甲氧虫酰肼

Q: 甲氧虫酰肼 的 CAS 号是多少？

甲氧虫酰肼 的 CAS 登记号为 161050-58-4。

Q: 甲氧虫酰肼 属于哪个分类？

所属分类：医药中间体及原料药。

CAS 161050-58-4C22H28N2O3MW 368.5

甲氧虫酰肼（CAS 161050-58-4）：分子式 C22H28N2O3、分子量 368.5；类别医药中间体及原料药。

产品描述

甲氧虫酰肼（CAS 161050-58-4）是一种医药中间体及原料药原料。其分子式 C22H28N2O3 由 22 个碳、28 个氢、2 个氮、3 个氧组成。分子量约为 368.5。公开物性数据显示其熔点约 206.2 - 208 °C、LogP 约 4.6。作为化工品采购代理与分销渠道，我们可在国内及跨境渠道为甲氧虫酰肼寻源比价，并安排小批量试样与批次采购；下单前提供完整 COA、质检报告与合规文件，验收以批次 COA 为准。

规格参数

CAS号161050-58-4

分子式C22H28N2O3

分子量368.5

熔点206.2 - 208 °C

LogP4.6

应用领域For methoxyfenozide (USEPA/OPP Pesticide Code: 121027) ACTIVE products with label matches. /SRP: Registered for use in the U.S. but approved pesticide uses may change periodically and so federal、state and local authorities must be consulted for currently approved uses./、Insecticide、This is a man-made compound that is used as a pesticide、Environmental transformation、predecessor)

类别医药中间体及原料药

用途与场景

登记用途：For methoxyfenozide (USEPA/OPP Pesticide Code: 121027) ACTIVE products with label matches. /SRP: Registered for use in the U.S. but approved pesticide uses may change periodically and so federal、state and local authorities must be consulted for currently approved uses./、Insecticide、This is a man-made compound that is used as a pesticide、Environmental transformation、predecessor)。

采购档案

这个产品是什么

甲氧虫酰肼是一种医药中间体或原料药类化合物，登记 CAS 号为 161050-58-4，分子式 C22H28N2O3（分子量 368.5），归属于医药中间体及原料药大类化工原料。

识别信息

登记 CAS 号：161050-58-4

其分子式 C22H28N2O3 由 22 个碳、28 个氢、2 个氮、3 个氧组成。

别名/同义词：甲氧虫酰肼 · Methoxyfenozide

所属分类：医药中间体及原料药

常见问题

甲氧虫酰肼的 CAS 号是多少？

甲氧虫酰肼的 CAS 登记号为 161050-58-4。

甲氧虫酰肼的分子式与分子量是多少？

分子式 C22H28N2O3，分子量 368.5。

甲氧虫酰肼还有哪些别名？

别名/同义词：甲氧虫酰肼、Methoxyfenozide。

甲氧虫酰肼的登记用途是什么？

甲氧虫酰肼属于哪个分类？

所属分类：医药中间体及原料药。

如何在 591daili.cn 采购甲氧虫酰肼？

请在联系页面提交产品名称、CAS 号与数量，我们作为采购代理在国内及跨境渠道为您寻源比价，安排试样与批次采购，下单前提供 COA 与合规文件。

包装与单证

包装按订单确认，从实验室小包装到吨袋大货，随订单安排而非在页面上写死。每批随货附 COA 分析证书，可另提供 MSDS；若终端用途带有法规限度（食品接触、药品或化妆品），请在询价时说明执行标准，等级按该标准确定。

PubChem 公开数据

甲氧虫酰肼（CAS 161050-58-4）的公开数据库记录，列此仅供独立核对。

危险化学品分类与危害说明

Reported hazard statements	H400 (69.9%), H410 (69.9%), H411 (30.1%), H401

H400 (69.9%): Very toxic to aquatic life [Warning Hazardous to the aquatic environment, acute hazard]

H410 (69.9%): Very toxic to aquatic life with long lasting effects [Warning Hazardous to the aquatic environment, long-term hazard]

物理形态与操作说明

White powder
In DMSO 11, cyclohexanone 9.9, acetone 9 (all in g/100g at 20 °C)
log Kow = 3.7 (shake flask)
When heated to decomposition it emits toxic vapors of /nitrogen oxides/.
201.9 Å² [M+Na]+ [CCS Type: DT; Buffer gas: N2; Ionization: ESI+; Dataset: TOXCAST; Source Identifier: DTXSID3032628]
194.2 Å² [M-H]- [CCS Type: DT; Buffer gas: N2; Ionization: ESI-; Dataset: TOXCAST; Source Identifier: DTXSID3032628]

公开数据库收录的理化数据

熔点	206.2 - 208 °C
熔点	MP: 204 - 20.6 °C /Technical/
溶解度	In water, 3.3 mg/L at 20 °C

这个物质在各数据库里的编号

CAS Registry Number	161050-58-4
PubChem CID	105010
分子式	C22H28N2O3
IUPAC 名称	N'-tert-butyl-N'-(3,5-dimethylbenzoyl)-3-methoxy-2-methylbenzohydrazide
UNII（FDA）	62A22651ZX

数据库记载的用途

The dermal absorption in vivo of methoxyfenozide formulated as an aqueous flow-able liquid (RH-112,485 2F) or as a wettable powder (RH-112,485 280WP) was tested in rats in a study that was designed to comply with US EPA guidelines and GLP. The methoxyfenozide administered was uniformly labelled with (14)C on the methoxyphenyl ring; this is acceptable given the limited cleavage seen in studies of oral metabolism. To provide data on exposure to the concentrated product and in-use-dilutions, groups of four male Crl :
Two metabolites, M16 (A-ring glucuronide of M14) and M26 (A-ring glucuronide of M24), were the main metabolites in bile. M16 was present at 13% and 18% in males and females respectively, M26 was present at 5% in males and 11% in females, all other metabolites represented <3% of the administered dose. The presence of M16 and M26 at higher concentrations in bile than in feces indicates that these two metabolites were subject to subsequent hydrolysis.
The primary /metabolic/ pathway probably involves demethylation of the A-ring methoxy moiety to form the corresponding phenol (M14), which is conjugated with glucuronic acid to form M16. Hydroxylation on the B-ring methyl moieties is also a significant metabolic pathway. Cleavage of methoxyfenozide to release either of the rings or the t-butyl group is only a minor pathway; none of the cleaved metabolites (M06, M07, M13, M32-36) were present at >2% of the dose. In males, however, cleaved metabolites represented up
Results for the animals receiving diets containing methoxyfenozide for 14 days plus a single dose of (14C) methoxyfenozide at 10 mg/kg bw by gavage showed evidence of induction of metabolism. Concentrations of M22, M28 and M30 increased, while concentrations of M14 and M24 were reduced relative to concentrations in animals that received only a single dose of (14C) methoxyfenozide at 10 mg/kg bw.

它在各数据库里的别名

Methoxyfenozide; 161050-58-4; Intrepid; N'-tert-Butyl-N'-(3,5-dimethylbenzoyl)-3-methoxy-2-methylbenzohydrazide; Runner; 3-Methoxy-2-methylbenzoic acid 2-(3,5-dimethylbenzoyl)-2-(1,1-dimethylethyl)hydrazide; Benzoic acid, 3-methoxy-2-methyl-, 2-(3,5-dimethylbenzoyl)-2-(1,1-dimethylethyl)hydrazide; RH-2485; DTXSID3032628; N'-(tert-butyl)-N'-(3,5-dimethylbenzoyl)-3-methoxy-2-methylbenzohydrazide; N-tert-butyl-N'-(3-methoxy-o-toluoyl)-3,5-xylohydrazide; 62A22651ZX; DTXCID1012628; CHEBI:38449; RH-112485; RefChem:157081

计算机算出的分子描述符

分子量	368.5
XLogP3	4.6
氢键供体数	1
氢键受体数	3
可旋转键数	4
精确质量	368.20999276
单同位素质量	368.20999276
拓扑极性表面积	58.6
重原子数	27
形式电荷	0

数据库摘要

Methoxyfenozide · CAS 161050-58-4 · C22H28N2O3. UNII 62A22651ZX. 熔点: 206.2 - 208 °C; 熔点: MP: 204 - 20.6 °C /Technical/; 溶解度: In water, 3.3 mg/L at 20 °C.

数据来源：PubChem / Wikidata；与随货 COA 不一致时以 COA 为准。

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