Duloxetine hydrochloride CAS NO.116539-59-4

• ProName: Duloxetine
• CasNo: 116539-59-4
• Molecular Formula: C18H19NOS
• Appearance: White or off-white Solid
• Application: Organic synthesis
• DeliveryTime: 20day
• PackAge: According to the demand of customer
• Port: shanghai
• ProductionCapacity: 20 Metric Ton/Week
• Purity: 98%
• Storage: Sealed, dry, microtherm , avoid light ...
• Transportation: by air or by sea
• LimitNum: 1 Kilogram
• Grade: Industrial Grade,Pharma Grade

• Depression, generalized anxiety disorder, and chronic musculoskeletal pain in the form of capsules and tablets.

 

Product Description        
  

• ProName:Factory Price API 99% Duloxetine 11653...
• CasNo:116539-59-4
• Molecular Formula:C18H19NOS
• Appearance:powder
• Application:API, pharmaceutical excipients, nutrit...
• DeliveryTime:Shiping within 3 working days after co...
• PackAge:1kg/bag; 25kg/drum, or as customer's r...
• Port:Any main ports of China
• ProductionCapacity:100 Metric Ton/Year
• Purity:98%~102%
• Storage:Far from fire and heat, keep in cool p...
• Transportation:DHL, EMS, FedEx, TNT, AIR, SEA
• LimitNum:1 Gram
• Related Substances:≤0.1%
• Residue on Ignition:≤0.05%
• Heavy Metal:<10ppm
• Valid Period:24 months

duloxetine basic information

product name:	duloxetine
synonyms:	duloxetine;duloxetine-d3;(s)-duloxetine;duloxetin;(3s)-n-methyl-3-naphthalen-1-yloxy-3-thiophen-2-yl-propan-1-amine;n-methyl-gama-(1-naphthalenyloxy)-2-thiophenepropanamine;duloxetine hci;duloxetine & intermediates
cas:	116539-59-4
mf:	c18h19nos
mw:	297.41
einecs:
product categories:	active pharmaceutical ingredients;api
mol file:	116539-59-4.mol

 

Product Name	Duloxetine
Synonyms	DULOXETINE;DULOXETINE-D3;(S)-DULOXETINE;DULOXETIN;(3S)-N-methyl-3-naphthalen-1-yloxy-3-thiophen-2-yl-propan-1-amine;N-Methyl-gama-(1-naphthalenyloxy)-2-thiophenepropanamine;DULOXETINE HCI;Duloxetine & Intermediates
CAS	116539-59-4
MF	C18H19NOS
MW	297.41
EINECS	1533716-785-6
Product Categories	ACTIVE PHARMACEUTICAL INGREDIENTS;API

 

 

Item	Standard
Structural data confirmation	1. H-NMR: The data of structure are identical with reference standard
	2. HPLC-MS: Ensure the molecular weight of main peak and fragment peak are identical with reference standard
	3. IR:The data of IR are identical with that of reference standard
Purity(HPLC)	≥99.0%
Related impurities	Specific single impurity	Meets EP/USP/BP standards
	Non-specific single impurity	≤0.10%
	Total Impurities	≤0.50%
Crystal form	Meets EP/USP/BP standards
Loss on drying	≤1.0%
Water	≤1.0%
Inorganic salt	≤0.1%
Heavy metals	≤10 ppm
Assay	98.0%~102.0%(According to EP/USP/BP standards)
Microbiological Analysis
Total plate count	≤1000cfu/g
Yeast and Moulds	≤100cfu/g
E. Coli.	Absent
Salmonella	Absent
S.aureus	Absent

 

 

 

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Zhejiang Huili Pharmaceutical Co., Ltd. is a professional pharmaceutical company which provide service for large pharmaceutical and health care products companies, such as: Collon Group, Sinopharm Group, and so on.

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