24种药物混标/BJS 201701|西域试剂

24种药物混标/BJS 201701,标准溶液,溶剂:甲醇, 100μg/mL

产品编号：西域质检-TM13532

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货号	包装	价格	库存与货期	购买量	操作
西域质检-TM13532		￥21000.00	杭州北京（现货）

增值税发票√顺丰快递√订货电话：18601927057

组分信息

CAS号	名称	标准值	单位
154-41-6	盐酸苯丙醇胺	100	μg/mL
50-98-6	盐酸麻黄碱	100	μg/mL
90-82-4	伪麻黄碱	100	μg/mL
552-79-4	甲基麻黄碱	100	μg/mL
300-62-9	苯丙胺	100	μg/mL
33817-09-3	脱氧麻黄碱	100	μg/mL
58-08-2	咖啡因	100	μg/mL
122-09-8	苯丁胺	100	μg/mL
846589-98-8	氯卡色林盐酸盐	100	μg/mL
31677-93-7	盐酸安非他酮	100	μg/mL
458-24-2	芬氟拉明	100	μg/mL
84484-78-6	N,N-双去甲基西布曲明盐酸盐	100	μg/mL
54910-89-3	氟西汀	100	μg/mL
77-09-8	酚酞	100	μg/mL
168835-59-4	N-单去甲基西布曲明	100	μg/mL
26807-65-8	吲达帕胺	100	μg/mL
84485-00-7	盐酸西布曲明	100	μg/mL
1446140-91-5	苄基西布曲明	100	μg/mL
935888-80-5	豪莫西布曲明盐酸盐	100	μg/mL
84485-08-5	盐酸氯代西布曲明	100	μg/mL
41859-67-0	苯扎贝特	100	μg/mL
28395-03-1	布美他尼	100	μg/mL
158681-13-1	盐酸利莫那班	100	μg/mL
49562-28-9	非诺贝特	100	μg/mL

详细介绍

24种药物混标/BJS 201701

Reference Material

This certificate is designed in accordance with ISO 17034 and ISO Guide 31. This reference material (RM) was designed,produced and verified in accordance with ISO/IEC 17025, ISO 17034 and a registered quality management system ISO 9001.

Product Name(产品名称) 24 Drug Mix in Methanol,100μg/mL(甲醇中24种药物混标)

Part Number(产品编号) 81809a

Lot Number(产品批号) 23010038

Expiry Date(失效日期) 2024-Feb-13____________________________________________________

Storage(存储条件) (-18±5)℃,Keep in the shade
冷冻(-18±5)℃,置于阴凉处

CERTIFIED
Component No. (组分数)	Concentration (μg/mL) (浓度)	Relative Expanded Uncertainty(%) (k=2) (相对扩展不确定度)
1	1	DL-Norephedrine Hydrochloride¹ (盐酸苯丙醇胺)	154-41-6	100	3
2	2	Ephedrine Hydrochloride¹ (盐酸麻黄碱)	50-98-6	100	3
3	2	Pseudoephedrine (伪麻黄碱)	90-82-4	100	3
4	3	(−)-N-Methylephedrine (甲基麻黄碱)	552-79-4	100	3
5	4	(±)-Amphetamine (苯丙胺)	300-62-9	100	3
6	5	(-)-Deoxyephedrine (脱氧麻黄碱)	33817-09-3	100	3
7	6	Caffeine (咖啡因)	58-08-2	100	3
8	7	Phentermine (苯丁胺)	122-09-8	100	3
9	8	Lorcaserin Hydrochloride¹ (氯卡色林盐酸盐)	846589-98-8	100	3
10	9	Bupropion Hydrochloride¹ (盐酸安非他酮)	31677-93-7	100	3
11	10	Fenfluramine (芬氟拉明)	458-24-2	100	3
12	11	N,N-Didesmethyl Sibutramine HCl¹ (N,N-双去甲基西布曲明盐酸盐)	84484-78-6	100	3
13	12	Fluoxetine (氟西汀)	54910-89-3	100	3
14	13	Desmethylsibutramine (N-单去甲基西布曲明)	168835-59-4	100	3
15	14	Sibutramine Hydrochloride¹ (盐酸西布曲明)	84485-00-7	100	3
16	15	Benzyl-sibutraMine (苄基西布曲明)	1446140-91-5	100	3
17	16	Homosibutramine Hydrochloride¹ (豪莫西布曲明盐酸盐)	935888-80-5	100	3
18	17	Chloro-sibutramine Hydrochloride¹ (盐酸氯代西布曲明)	84485-08-5	100	3
19	18	Phenolphthalein (酚酞)	77-09-8	100	3
20	19	Indapamide (吲达帕胺)	26807-65-8	100	3
21	20	Bezafibrate (苯扎贝特)	41859-67-0	100	3
22	21	Bumetanide (布美他尼)	28395-03-1	100	3
23	22	Rimonabant Hydrochloride¹ (盐酸利莫那班)	158681-13-1	100	3
24	23	Fenofibrate (非诺贝特)	49562-28-9	100	3

Intended Use

This RM is intended for use in a laboratory as a calibration and quality control standard or in method development for analytical techniques.

Uncertainty

The certified value(s) and uncertainty(ies) are determined in accordance with ISO 17034 with an 95% confidence level (k=2). Uncertainty is based on the Total Combined Uncertainty, including uncertainties of preparation, purity of neat materials, homogeneity, stability testing.

Traceability

The balances used for gravimetric measurements are calibrated with weights traceable to the national standards. The calibration of the balances is verified annually by an external accredited calibration service. This analysis method has been verified using an approach consistent with ISO 17034:2016 & ISO 17025:2017.

Homogeneity

Random replicate samples of the final packaged RM have been analysed to prove homogeneity consistent with ISO 17034.

Storage

The RM should be stored in the original sealed bottle at the indicated temperature.