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Linezolid-d8

CAS No.
1032182-14-1
Chemical Name:
Linezolid-d8
Synonyms
Linezolid-d8;Acetamide, N-[[(5S)-3-[3-fluoro-4-(4-morpholinyl-2,2,3,3,5,5,6,6-d8)phenyl]-2-oxo-5-oxazolidinyl]methyl]-
CBNumber:
CB82610997
Molecular Formula:
C16H12D8FN3O4
Molecular Weight:
345.4
MDL Number:
MOL File:
1032182-14-1.mol
MSDS File:
SDS
Last updated:2026-05-28 05:32:35

Linezolid-d8 Properties

NACRES NA.24

SAFETY

Risk and Safety Statements

Symbol(GHS)  Flame (GHS02)Skull and Crossbones (GHS06)Health Hazard (GHS08)
GHS02,GHS06,GHS08
Signal word  Danger
Hazard statements  H225-H301+H311+H331-H370
Precautionary statements  P210-P233-P280-P301+P310-P303+P361+P353-P304+P340+P311
target organs Eyes,Central nervous system
WGK Germany  WGK 2
Storage Class 3 - Flammable liquids
Hazard Classifications Acute Tox. 3 Dermal
Acute Tox. 3 Inhalation
Acute Tox. 3 Oral
Flam. Liq. 2
STOT SE 1

Linezolid-d8 price

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
ChemScene CS-0380601 Linezolid-d8 99.73% 1032182-14-1 1mg $1051 2026-06-04 Buy
ChemScene CS-0380601 Linezolid-d8 99.73% 1032182-14-1 5mg $3705 2026-06-04 Buy
Product number Packaging Price Buy
CS-0380601 1mg $1051 Buy
CS-0380601 5mg $3705 Buy

Linezolid-d8 Chemical Properties, Uses, Production

Uses

PNU-100766-d8 is deuterated labeled Linezolid (HY-10394). Linezolid (PNU-100766) is the first member of the class of oxazolidinone synthetic antibiotic. Linezolid acts by inhibiting the initiation of bacterial protein synthesis. Linezolid is used for the treatment of serious infections caused by Gram-positive bacteria that are resistant to several other antibiotics[1][2][3].

References

[1] Russak EM, et al. Impact of Deuterium Substitution on the Pharmacokinetics of Pharmaceuticals. Ann Pharmacother. 2019 Feb;53(2):211-216. DOI:10.1177/1060028018797110
[2] Clemett D, Markham A. Linezolid. Drugs. 2000 Apr;59(4):815-27; discussion 828. DOI:10.2165/00003495-200059040-00007
[3] Chiappini E, Conti C, Galli L et al. Clinical efficacy and tolerability of linezolid in pediatric patients: a systematic review. Clin Ther. 2010 Jan;32(1):66-88. DOI:10.1016/j.clinthera.2010.01.019
[4] Perry CM, Jarvis B. Linezolid: a review of its use in the management of serious gram-positive infections. Drugs. 2001;61(4):525-51. DOI:10.2165/00003495-200161040-00008
[5] He MZ, Jiang YW, Cai C. Mechanisms and epidemiology of linezolid resistance in staphylococci.Zhonghua Jie He He Hu Xi Za Zhi. 2012 May;35(5):360-2. PMID:22883997
[6] Karau MJ, Tilahun AY, Schmidt SM, Clark CR, Patel R, Rajagopalan G. Linezolid is Superior to Vancomycin in Experimental Pneumonia Caused by Superantigen-Producing Staphylococcus aureus in HLA class II Transgenic Mice. Antimicrob Agents Chemother. 2012 Jul 30. DOI:10.1128/AAC.01080-12

Linezolid-d8 Preparation Products And Raw materials

Raw materials

Preparation Products

Linezolid-d8 Suppliers

Global Suppliers ( 8)
Supplier Tel Email Country ProdList Advantage
Quality Control Solutions Ltd. 0755-66853366 13670046396 orders@qcsrm.com China 18188 56
Pushan Industry (Shaanxi) Co., Ltd. 029-81310890 18165209495 2929288192@qq.com China 9949 58
Shanghai YuZn Pharm. Technology Co.,Ltd. 15921286451; 15921286451 2010681527@qq.com China 4918 58
Shandong Dayou Pharmaceutical Research and Development Co., Ltd. hanfangpharma@126.com 15165037910 hanfangpharma@126.com China 25800 58
Changzhou Xianglong Pharmaceutical Technology Co., Ltd., 18915873328 18915873328 sales@xianglongpharm.com China 11049 58
Linezolid-d8 Acetamide, N-[[(5S)-3-[3-fluoro-4-(4-morpholinyl-2,2,3,3,5,5,6,6-d8)phenyl]-2-oxo-5-oxazolidinyl]methyl]- 1032182-14-1