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ChemicalBook >> CAS DataBase List >>SCOPOLAMINE METHYL NITRATE

SCOPOLAMINE METHYL NITRATE

CAS No.
6106-46-3
Chemical Name:
SCOPOLAMINE METHYL NITRATE
Synonyms
METHSCOPOLAMINE NITRATE;skopyl;viscope;mescomine;skopolate;itrate,(-)-tropate;HYOSCINEMETHONITRATE;Scopolamine (nitrate);dwithmethylnitrate1:1);HYOSCINE METHYL NITRATE
CBNumber:
CB2453455
Molecular Formula:
C18H24NO4.NO3
Molecular Weight:
380.39
MDL Number:
MFCD00078239
MOL File:
6106-46-3.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-05-28 00:29:52
Product description Number Pack Size Price
Scopolamine Methyl Nitrate >98.0%(HPLC)(T) S0230 1g $167
Scopolamine Methyl Nitrate >98.0%(HPLC)(T) S0230 5g $424
Scopolamine methyl nitrate ≥98% CS-0185900 1g $332
Scopolamine methyl nitrate ≥98% CS-0185900 1g $332
Scopolamine methyl nitrate ≥99%(Assaybytitration,HPLC) 32523 100MG $50
More product size

SCOPOLAMINE METHYL NITRATE Properties

Melting point 199 °C
refractive index -25 ° (C=1, H2O)
Water Solubility almost transparency in Water
form powder to crystal
color White to Almost white
Merck 14,8406
CAS DataBase Reference 6106-46-3(CAS DataBase Reference)
FDA UNII K0813KQM3V
EPA Substance Registry System Methylscopolamine nitrate (6106-46-3)

SAFETY

Risk and Safety Statements

Symbol(GHS)  Skull and Crossbones (GHS06)
GHS06
Signal word  Danger
Hazard statements  H330-H300-H310
Precautionary statements  P260-P271-P284-P304+P340-P310-P320-P403+P233-P405-P501-P262-P264-P270-P280-P302+P350-P310-P322-P361-P363-P405-P501-P264-P270-P301+P310-P321-P330-P405-P501
Hazard Codes  T,T+
Risk Statements  23/24/25-26/27/28
Safety Statements  36/37/39-45-25
RIDADR  UN 1544 6.1/PG 3
WGK Germany  3
RTECS  YM3675150
TSCA  TSCA listed
HS Code  2939.80.0000
HazardClass  6.1
PackingGroup  III
Hazardous Substances Data 6106-46-3(Hazardous Substances Data)
NFPA 704
0
4 0

SCOPOLAMINE METHYL NITRATE price More Price(19)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
TCI Chemical S0230 Scopolamine Methyl Nitrate >98.0%(HPLC)(T) 6106-46-3 1g $167 2026-04-30 Buy
TCI Chemical S0230 Scopolamine Methyl Nitrate >98.0%(HPLC)(T) 6106-46-3 5g $424 2026-04-30 Buy
ChemScene CS-0185900 Scopolamine methyl nitrate ≥98% 6106-46-3 1g $332 2026-06-04 Buy
ChemScene CS-0185900 Scopolamine methyl nitrate ≥98% 6106-46-3 1g $332 2026-06-04 Buy
Chem-Impex 32523 Scopolamine methyl nitrate ≥99%(Assaybytitration,HPLC) 6106-46-3 100MG $50 2026-05-19 Buy
Product number Packaging Price Buy
S0230 1g $167 Buy
S0230 5g $424 Buy
CS-0185900 1g $332 Buy
CS-0185900 1g $332 Buy
32523 100MG $50 Buy

SCOPOLAMINE METHYL NITRATE Chemical Properties,Uses,Production

Originator

Transderm ,Scop Novartis Consumer Health Inc.

Uses

(-)Scopolamine Methylnitrate is a competitive antimuscarinic agent.

Manufacturing Process

In a one-liter separatory funnel, 94 g (0.215 mol) of scopolamine hydrobromide trihydrate was dissolved in 250 ml of water, made alkaline by shaking with 40 g (1 mol) of sodium hydroxide in 150 ml of water, and the free base immediately extracted with ether. As scopolamine is somewhat soluble in water, the aqueous layer was saturated with potassium carbonate and again extracted with ether. The combined ether extracts were dried over anhydrous magnesium sulfate and the ether removed by distillation, leaving 65 g (0.214 mol; 100% yield) of nearly colorless oil. Then 100 g (1.05 mol) of cold methyl bromide was added to a chilled, 500-ml pressure flask containing the 65 g of scopolamine, the flask stoppered tightly with a clamp, and allowed to stand at room temperature for 96 hours. The flask was cooled before opening, excess methyl bromide removed by distilling, and the white solid washed thoroughly with dry ether. The yield of crude Nmethylscopolammonium bromide was 80 g (94 %t yield). The salt was recrystallized from 550 ml of alcohol; first crop, 70 g, MP: 212-214°C; second crop, 6 g, melting point 195-200°C. The combined crops were again recrystallized from 500 ml of alcohol; melting point 210-212°C. The third recrystallization from 600 ml of alcohol yielded 64 g, melting point 214- 216°C, a 75 % yield based on scopolamine hydro-bromide trihydrate starting material. N-Methylscopolammonium bromide may be dissolved in water. An equivalent of solution AgNO3 was added, a precipitated AgBr was filtered off. The filtrate was evaporated to dryness to give the desired Nmethylscopolammonium nitrate.

brand name

Mesconit;Skopyle.

Therapeutic Function

Anticholinergic, Spasmolytic

World Health Organization (WHO)

Hyoscine methonitrate, a quaternary ammonium anticholinergic agent, was introduced in 1947 for use as a gastrointestinal antispasmodic. The action taken in Sweden relates to the use of this compound in preparations for suppressing the appetite. Preparations may remain available elsewhere.

SCOPOLAMINE METHYL NITRATE Preparation Products And Raw materials

Global( 86)Suppliers
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(-)SCOPOLAMINE METHYL NITRATE SCOPOLAMINE METHYL NITRATE HYOSCINE METHYL NITRATE ,9-dimethyl-,[7(s)-(1alpha,2beta,4beta,5alpha,7beta)]-,nitrate(salt) 1alphah,5alphah-tropanium,6beta,7beta-epoxy-3alpha-hydroxy-8-methyl-,nitrate, 4)non-7-ylester,(7(s)-(1alpha,2beta,4beta,5alpha,7beta))-.0comp 5-alpha-h-tropanium,6-beta,7-beta-epoxy-3-alpha-hydroxy-8-methyl-1-alpha-n 9-dimethyl--(7(s)-(1alpha,2beta,4beta,5alpha,7beta))--nitrate(salt) alpha,-(hydroxymethyl)-benzeneaceticaci9-methyl-3-oxa-9-aztricyclo(3.3.1 dwithmethylnitrate1:1) epoxytropinetropatemethylnitrate itrate,(-)-tropate mescomine methylnitrate,compdwithscopolamine methylscopolaminenitrate n-methylscopolammoniumnitrate scopolamine,compdwithmethylnitrate(1:1) skopolate skopyl viscope HYOSCINEMETHONITRATE (-)-Scopolaminmethylnitrat (-)-N-methylhyoscinium nitrate Hyoscine methyl nitrate, Methscopolamine nitrate METHYL HYOSCINE NITRATE Scopolamine Methyl Nitrate > (-)Scopolamine Methylnitrate Scopolamine (nitrate) (-)-Scopolamine methyl nitrate 3-Oxa-9-azoniatricyclo[3.3.1.02,4]nonane, 7-[(2S)-3-hydroxy-1-oxo-2-phenylpropoxy]-9,9-dimethyl-, (1α,2β,4β,5α,7β)-, nitrate (1:1) SCOPOLAMINE compounded with METHYL NITRATE (1:1) METHSCOPOLAMINE NITRATE 6106-46-3 C17H21NO4CH3NO3 C18H24N2O7 C18H24NO4NO3 Tropane Alkaloids Alkaloids Alkaloids Biochemistry Tropane Alkaloids
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