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101-31-5

101-31-5 structure
101-31-5 structure
  • Name: Hyoscyamine
  • Chemical Name: (S)-atropine
  • CAS Number: 101-31-5
  • Molecular Formula: C17H23NO3
  • Molecular Weight: 289.369
  • Catalog: API Digestive system medication Gastrointestinal expectorant
  • Create Date: 2018-02-06 08:00:00
  • Modify Date: 2026-07-23 20:49:45
  • L-Hyoscyamine is a chemical compound, a tropane alkaloid it is the levo-isomer to atropine.Target: mAChRHyoscyamine is a chemical compound, a tropane alkaloid it is the levo-isomer to atropine. It is a secondary metabolite of some plants, particularly henbane (Hyoscamus niger.)Hyoscyamine is used to provide symptomatic relief to various gastrointestinal disorders including spasms, peptic ulcers, irritable bowel syndrome, pancreatitis, colic and cystitis. It has also been used to relieve some heart problems, control some of the symptoms of Parkinson's disease, as well as for control of respiratory secretions in end of life care [1].

Name (S)-atropine
Synonyms CYSTOSPAZ
[3(S)-endo]-α-(Hydroxymethyl)benzeneacetic acid 8-methyl-8-azabicyclo[3.2.1]oct-3-yl ester
Benzeneacetic acid, α-(hydroxymethyl)-, 8-methyl-8-azabicyclo[3.2.1]oct-3-yl ester, [3(S)-endo]
L-Hyoscyamine
3a-Tropanyl S-(-)-Tropate
L-Hyoscyamine (Daturine)
Alpha-(Hydroxymethyl)-Benzeneaceticaci8-Methyl-8-Azabicyclo[3.2.1]
L-DATURINE
Monoclonal Anti-LPA antibody produced in mouse
(S)-(-)-hyoscyamine
AK38
(-)-tropicaciesterwithtropine
SCOPINE TROPATE HYDROCHLORIDE
[3(S)-ENDO]-8-METHYL-8-AZABICYCLO[3.2.1]OCT-3-YL ESTER, ALPHA-(HYDROXYMETHYL)-BENZENEACETIC ACID
l-Hyopscyamine
DATURINE
L-Hyoscamine
MFCD00067306
L-DUBOISINE
EINECS 202-933-0
Cystospaz
[3(s)-endo]-leste
L-TROPINE TROPATE
Daturine
alpha-(hydroxymethyl)-benzeneaceticaci8-methyl-8-azabicyclo(3.2.1)oct-3-y
SSECS
Egacene
[S,(-)]-α-(Hydroxymethyl)benzeneacetic acid (1R,5S)-8-methyl-8-azabicyclo[3.2.1]octan-3α-yl
(-)-atropine
[3(S)-endo]-a-(Hydroxymethyl)benzeneacetic Acid 8-Methyl-8-azabicyclo[3.2.1]oct-3-yl Ester
(S)-(-)-Hyoscyamine
L-Tropine tropate
L-Hyoscyamin
(-)-Hyoscyamine from Atropa belladonna L
Levsinex
(-)-hyoscyamin
L-HYOSCYAMINE FREE BASE CRYSTALLINE
DKFZp434B1417
Anti-SSECS antibody produced in rabbit
M161491
Benzeneacetic acid, α-(hydroxymethyl)-, (3-endo)-8-methyl-8-azabicyclo[3.2.1]oct-3-yl ester, (αS)
(3-endo)-8-Methyl-8-azabicyclo[3.2.1]oct-3-yl-(2S)-3-hydroxy-2-phenylpropanoat
L-(P)
HYOSCYAMINE, L-(P)
scopolamine HCl
(S)-Atropine
Tropic acid, 1alphaH,5alphaH-tropan-3alpha-yl ester, (-)
SCOPINE TROPATE
Levsin
(-)-HYOSCYAMINE
(3-endo)-8-Methyl-8-azabicyclo[3.2.1]oct-3-yl (2S)-3-hydroxy-2-phenylpropanoate
Hyoscamine
Hyocyamine
(3(s)-endo)-leste
Duboisine
HYOSCYAMINE
1αH,5αH-Tropan-3α-yl (-)-tropate
l-Atropine
1-Hyoscyamine
BENZENEACETIC ACID, ALPHA-(HYDROXYMETHYL)-, 8-METHYL-8-AZABICYCLO[3.2.1]OCT-3-YL ESTER, [3(S)-ENDO]
(8-Methyl-8-azabicyclo[3.2.1]octan-3-yl) (2S)-3-hydroxy-2-phenylpropanoate
alpha-(hydroxymethyl)-benzeneaceticaci8-methyl-8-azabicyclo[3.2.1]oct-3-y
(-)-Hycosamine
(-)-Hyoscyamine
Tropic acid, 1αH,5αH-tropan-3α-yl ester, (-)- (8CI)
Benzeneacetic acid, .alpha.-(hydroxymethyl)-, (3-endo)-8-methyl-8-azabicyclo3.2.1oct-3-yl ester, (.alpha.S)
L-Hyoscyamine free base
chlorhydratedescopolamine
Belladonna Liquid Extract/hyoscyamine
1-Tropic Acid Ester with Tropine
(2S)-3-hydroxy-2-phenylpropanoic acid [(1R,5S)-8-methyl-8-azoniabicyclo[3.2.1]octan-3-yl] ester
er),hcl
HYOSCYAMINEL
Peptard
ScopolamineSeries
Benzeneacetic acid, a-(hydroxymethyl)-,(3-endo)-8-methyl-8-azabicyclo[3.2.1]oct-3-yl ester, (aS)
(2S)-(1R,5S)-8-Methyl-8-azabicyclo[3.2.1]octan-3-yl 3-hydroxy-2-phenylpropanoate
L-HYOSCYAMINE
1aH,5aH-Tropan-3a-ol(-)-tropate (Ester)
Description L-Hyoscyamine is a chemical compound, a tropane alkaloid it is the levo-isomer to atropine.Target: mAChRHyoscyamine is a chemical compound, a tropane alkaloid it is the levo-isomer to atropine. It is a secondary metabolite of some plants, particularly henbane (Hyoscamus niger.)Hyoscyamine is used to provide symptomatic relief to various gastrointestinal disorders including spasms, peptic ulcers, irritable bowel syndrome, pancreatitis, colic and cystitis. It has also been used to relieve some heart problems, control some of the symptoms of Parkinson's disease, as well as for control of respiratory secretions in end of life care [1].
Related Catalog
References

[1]. http://www.drugbank.ca/drugs/DB00424

Density 1.2±0.1 g/cm3
Boiling Point 429.8±45.0 °C at 760 mmHg
Melting Point 108.5ºC
Molecular Formula C17H23NO3
Molecular Weight 289.369
Flash Point 213.7±28.7 °C
Exact Mass 289.167786
PSA 49.77000
LogP 1.53
Vapour Pressure 0.0±1.1 mmHg at 25°C
Index of Refraction 1.581
Storage condition 2-8°C

CHEMICAL IDENTIFICATION

RTECS NUMBER :
NH0875000
CHEMICAL NAME :
Hyoscyamine, (-)-
CAS REGISTRY NUMBER :
101-31-5
LAST UPDATED :
199701
DATA ITEMS CITED :
4
MOLECULAR FORMULA :
C17-H23-N-O3
MOLECULAR WEIGHT :
289.41
WISWESSER LINE NOTATION :
T56 A ANTJ A1 GOVYR&1Q -L

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

TYPE OF TEST :
LDLo - Lowest published lethal dose
ROUTE OF EXPOSURE :
Unreported
SPECIES OBSERVED :
Human - man
DOSE/DURATION :
1471 ug/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
85DCAI "Poisoning; Toxicology, Symptoms, Treatments," 2nd ed., Arena, J.M., Springfield, IL, C.C. Thomas, 1970 Volume(issue)/page/year: 2,73,1970
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Intravenous
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
95 mg/kg
TOXIC EFFECTS :
Sense Organs and Special Senses (Eye) - effect, not otherwise specified Behavioral - convulsions or effect on seizure threshold Lungs, Thorax, or Respiration - dyspnea
REFERENCE :
BJPCAL British Journal of Pharmacology and Chemotherapy. (London, UK) V.1-33, 1946-68. For publisher information, see BJPCBM. Volume(issue)/page/year: 24,138,1965 *** NIOSH STANDARDS DEVELOPMENT AND SURVEILLANCE DATA *** NIOSH OCCUPATIONAL EXPOSURE SURVEY DATA : NOHS - National Occupational Hazard Survey (1974) NOHS Hazard Code - A1029 No. of Facilities: 68 (estimated) No. of Industries: 1 No. of Occupations: 6 No. of Employees: 2770 (estimated)
Hazard Codes T+: Very toxic;
Risk Phrases R26/28
Safety Phrases 24-45
RIDADR UN 1544 6
WGK Germany 3
RTECS NH0875000
HS Code 2933990090

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101-31-5

Literature: Phytochemistry (Elsevier), , vol. 28, # 12 p. 3507 - 3510

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101-31-5

Literature: Journal of Natural Products, , vol. 69, # 9 p. 1335 - 1340

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101-31-5

Literature: Archiv der Pharmazie (Weinheim, Germany), , vol. 240, p. 501

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101-31-5

Literature: Journal of the Chemical Society, , vol. 101, p. 950

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101-31-5

Literature: Journal of the Chemical Society, , vol. 95, p. 1966

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101-31-5 structure

101-31-5

Literature: Chemistry Letters, , p. 983 - 986
HS Code 2933990090
Summary 2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%
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