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(S)-(+)-NOREPINEPHRINE L-BITARTRATE

Product Name
(S)-(+)-NOREPINEPHRINE L-BITARTRATE
CAS No.
636-88-4
Chemical Name
(S)-(+)-NOREPINEPHRINE L-BITARTRATE
Synonyms
Imidacloprid Impurity 29;(+)-Noradrenaline Bitartrate;(S)-(+)-NOREPINEPHRINE L-BITARTRATE;D-Norepinephrine hydrogen tartrate salt;D-Noradrenaline (Norepinephrine) Bitartrate;4-[(1S)-2-amino-1-hydroxy-ethyl]pyrocatechol;(S)-4-(2-amino-1-hydroxyethyl)benzene-1,2-diol;4-[(1S)-2-amino-1-hydroxyethyl]benzene-1,2-diol;4-[(1S)-2-azanyl-1-hydroxy-ethyl]benzene-1,2-diol;Epinephrine Impurity 13 2 Tartrate(D-Norepinephrine
CBNumber
CB3388503
Molecular Formula
C12H17NO9
Formula Weight
319.27
MOL File
636-88-4.mol
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(S)-(+)-NOREPINEPHRINE L-BITARTRATE Property

Melting point:
166 °C (dec.)(lit.)
storage temp. 
2-8°C
solubility 
DMSO (Slightly), Methanol (Slightly, Heated), Water (Slightly, Sonicated)
form 
Solid
color 
White to Off-White
optical activity
[α]20/D +38°, c = 1 in H2O
Stability:
Hygroscopic
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Safety

Hazard Codes 
T,Xn
Risk Statements 
25-36/37/38-20/21/22
Safety Statements 
36/37-45-37/39-26
RIDADR 
UN 2811 6.1/PG 3
WGK Germany 
3
F 
8-10-23
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Danger
Hazard statements

H301Toxic if swalloed

Precautionary statements

P301+P310IF SWALLOWED: Immediately call a POISON CENTER or doctor/physician.

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
407453
Product name
(S)-(+)-Norepinephrine L-bitartrate
Purity
99%
Packaging
1g
Price
$1160
Updated
2022/05/15
TRC
Product number
N661025
Product name
(+)-NoradrenalineBitartrate
Packaging
10mg
Price
$180
Updated
2021/12/16
Biosynth Carbosynth
Product number
FA146097
Product name
4-[(1S)-2-Amino-1-Hydroxy-Ethyl]Benzene-1,2-Diol
Packaging
50mg
Price
$70
Updated
2021/12/16
Biosynth Carbosynth
Product number
FA146097
Product name
4-[(1S)-2-Amino-1-Hydroxy-Ethyl]Benzene-1,2-Diol
Packaging
100mg
Price
$105
Updated
2021/12/16
Matrix Scientific
Product number
096279
Product name
(S)-(+)-Norepinephrine L-bitartrate
Purity
95+%
Packaging
250mg
Price
$189
Updated
2021/12/16
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(S)-(+)-NOREPINEPHRINE L-BITARTRATE Chemical Properties,Usage,Production

Uses

(+)-Noradrenaline Bitartrate is an agonist at a1- and a2-adrenoreceptors.

Purification Methods

Recrystallise adrenor from EtOH and store it in the dark under N2. [pKa, Lewis Brit J Pharmacol Chemother 9 488 1954, UV: Bergstr.m et al. Acta Physiol Scand 20 101 1950, Fluorescence: Bowman et al. Science NY 122 32 1955, Tullar J Am Chem Soc 70 2067 1948.] The L-tartrate salt monohydrate has m 102-104.5o, [] D -11o (c 1.6, H2O), after recrystallisation from H2O or EtOH. [Beilstein 13 III 2382.]

(S)-(+)-NOREPINEPHRINE L-BITARTRATE Preparation Products And Raw materials

Raw materials

Preparation Products

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(S)-(+)-NOREPINEPHRINE L-BITARTRATE Suppliers

China 41 Germany 1 India 4 Switzerland 1 United Kingdom 2 United States 3 Global 52
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16314854226
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info@bocsci.com
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Matrix Scientific
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636-88-4, (S)-(+)-NOREPINEPHRINE L-BITARTRATERelated Search:

Isoproterenol Aminophylline Norepinephrine 3,4-DIHYDROXYBENZYL ALCOHOL

  • ALPHA-(AMINOMETHYL)-3,4-DIHYDROXYBENZYL ALCOHOL L-BITARTRATE
  • (S)-(+)-NOREPINEPHRINE L-BITARTRATE
  • D-Norepinephrine hydrogen tartrate salt
  • (S)-beta,3,4-trihydroxyphenethylammonium [R-(R*,R*)]-hydrogen tartrate
  • D-Noradrenaline L-bitartrate, D-Noradrenaline hydrogen L-tartrate, D-Norepinephrine D-bitartrate, (+)-α-(Aminomethyl)-3,4-dihydroxybenzyl alcohol (+)-tartrate (1:1)
  • D-Arterenol hydrogen tartrate salt, D-Noradrenaline hydrogen tartrate salt, D-Norepinephrine bitartrate
  • 4-[(1S)-2-amino-1-hydroxyethyl]benzene-1,2-diol
  • 4-[(1S)-2-amino-1-hydroxy-ethyl]pyrocatechol
  • 4-[(1S)-2-azanyl-1-hydroxy-ethyl]benzene-1,2-diol
  • (S)-4-(2-amino-1-hydroxyethyl)benzene-1,2-diol(2R,3R)-2,3-dihydroxysuccinate
  • (+)-Noradrenaline Bitartrate
  • D-Noradrenaline (Norepinephrine) Bitartrate
  • (S)-4-(2-amino-1-hydroxyethyl)benzene-1,2-diol
  • Epinephrine Impurity 2 Tartrate(D-Norepinephrine Bitartrate)
  • Imidacloprid Impurity 29
  • Epinephrine Impurity 13 2 Tartrate(D-Norepinephrine
  • 636-88-4
  • HO2C6H3CHCH2NH2OHC4H6O6
  • C12H17O9N
  • Organic Building Blocks
  • Amino Alcohols
  • Chiral Building Blocks
  • Asymmetric Synthesis