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Rocuronium bromide (CAS No.: 119302-91-9)

Manus Aktteva Biopharma LLP is an ISO 9001:2015 Certified Global Supplier based in India for the product Rocuronium bromide, 119302-91-9.
We offer the product Rocuronium bromide, 119302-91-9 from our manufacturer / supplier / principals for your Research and Development / Evaluation or Commercial requirements, based on the product's availability from our network. We can also offer Rocuronium bromide, 119302-91-9 intermediates with the supportive technical package required for evaluation.
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CAS number:

119302-91-9

Chemical Name:

[3-Hydroxy-10,13-dimethyl-2-morpholin-4-yl-16-(1-prop-2-enyl-2,3,4,5-tetrahydropyrrol-1-yl)-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl] acetate bromide, Rocuronium bromide (CAS No.: 119302-91-9)

Pharmacopeia:

USP, EP, BP, In House

Manufacturer Certificate:

GMP, Factory GMP, cGMP, EUGMP, WHO GMP, ISO Certified, USFDA

Application:

For R&D Purpose

Properties
Related Intermediates

Synonym

[3-Hydroxy-10,13-dimethyl-2-morpholin-4-yl-16-(1-prop-2-enyl-2,3,4,5-tetrahydropyrrol-1-yl)-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl] acetate bromide, Rocuronium bromide (CAS No.: 119302-91-9)

Molecular Formula

C32H53N2O4.Br

Molecular Weight

609.69

Manufacturer Specifications

Available on request

Packing

Export worthy packing

Material Safety Data Sheet

Available on request

Availability

FOR R&D PORPOSE

Product Name	CAS No.
(2b,3a,5a,16b,17b)-2-(4-Morpholinyl)-16-(1-pyrrolidinyl)androstane-3,17-diol	119302-20-4	View \| Inquire
(2b,3a,5a,16b,17b)-17-Acetoxy-3-hydroxy-2-(4-morpholinyl)-16-(1-pyrrolidinyl)androstane	119302-24-8	View \| Inquire

Description:

Rocuronium (Zemuron, Esmeron) is an aminosteroid non-depolarizing neuromuscular blocker or muscle relaxant used in modern anaesthesia.

Manufacturer Documentation / Approvals :

USDMF	EDMF	DMF (OPEN PART)	DMF (CLOSED PART)	TDP	DMF - CTD

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Products currently covered by valid US Patents are offered for R&D use from a manufacturer in accordance with 35 USC 271 +A13(1)
Products falling in to controlled substance category / list of schedule drugs shall be exported directly from the manufacturer principals only against receipt of original import permission issued by concerned authorities of the importing country.
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