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(-)-2-Aminobuttersure

L(+)-2-Aminobutyric acid Struktur
1492-24-6
CAS-Nr.
1492-24-6
Bezeichnung:
(-)-2-Aminobuttersure
Englisch Name:
L(+)-2-Aminobutyric acid
Synonyma:
AMINOBUTYRIC ACID;L-2-AMINOBUTYRIC ACID;2-AMINOBUTANOIC ACID;L-ABU;H-ABU-OH;L-ALPHA-AMINOBUTYRIC ACID;L-2-AMINOBUTANOIC ACID;L-2-Abu;L-ABU-OH;Z-&gamma
CBNumber:
CB3741533
Summenformel:
C4H9NO2
Molgewicht:
103.12
MOL-Datei:
1492-24-6.mol

(-)-2-Aminobuttersure Eigenschaften

Schmelzpunkt:
300 °C
Siedepunkt:
215.2±23.0 °C(Predicted)
alpha 
21.6 º (c=2, 5N HCl)
Dichte
1.2300 (estimate)
Brechungsindex
1.4650 (estimate)
storage temp. 
room temp
L?slichkeit
22.7 g/100 mL (22°C)
pka
2.29(at 25℃)
Aggregatzustand
Crystalline Powder
Farbe
White to beige
Biologische Quelle
Porcine kidney
microbial
plant
Wasserl?slichkeit
22.7 g/100 mL (22 ºC)
Merck 
14,428
BRN 
1720935
InChIKey
QWCKQJZIFLGMSD-VKHMYHEASA-N
CAS Datenbank
1492-24-6(CAS DataBase Reference)
NIST chemische Informationen
(l)-2-Aminobutanoic acid(1492-24-6)
EPA chemische Informationen
Butanoic acid, 2-amino-, (2S)- (1492-24-6)
Sicherheit
  • Risiko- und Sicherheitserkl?rung
  • Gefahreninformationscode (GHS)
Kennzeichnung gef?hrlicher Xi
R-S?tze: 43
S-S?tze: 36/37
WGK Germany  3
Hazard Note  Irritant
TSCA  Yes
HS Code  29224999
Bildanzeige (GHS) GHS hazard pictograms
Alarmwort Warnung
Gefahrenhinweise
Code Gefahrenhinweise Gefahrenklasse Abteilung Alarmwort Symbol P-Code
H317 Kann allergische Hautreaktionen verursachen. Sensibilisierung der Haut Kategorie 1A Warnung GHS hazard pictogramssrc="/GHS07.jpg" width="20" height="20" /> P261, P272, P280, P302+P352,P333+P313, P321, P363, P501
Sicherheit
P280 Schutzhandschuhe/Schutzkleidung/Augenschutz tragen.

(-)-2-Aminobuttersure Chemische Eigenschaften,Einsatz,Produktion Methoden

R-S?tze Betriebsanweisung:

R43:Sensibilisierung durch Hautkontakt m?glich.

S-S?tze Betriebsanweisung:

S36/37:Bei der Arbeit geeignete Schutzhandschuhe und Schutzkleidung tragen.

Chemische Eigenschaften

White Crystalline Solid

Definition

ChEBI: An optically active form of alpha-aminobutyric acid having L-configuration.

Allgemeine Beschreibung

L-2-Aminobutyric acid is synthesized from L-threonine and L-aspartic acid through a ?-transamination reaction. It is an L-alanine analogue with an ethyl side chain.

Synthese

The preparation of l-2-aminobutyric acid (l-ABA) is mainly achieved by chemical synthesis or enzymatic conversion. In chemical methods, synthesis of l-ABA has been extensively reported, including ammonolysis of α-halogen acid, reduction reaction, ammoniation hydrolysis reaction and butanone acid reduction. However, the obvious disadvantages of chemical synthesis, such as poor selectivity, harsh reaction conditions, various byproducts, and the difficulty in separation and purification, limited its development. It is reported that l-ABA was synthesized in a transamination reaction from α-ketobutyric acid and l-aspartic acid as substrates using aromatic aminotransferase or produced from α-ketobutyric acid and benzylamine using ω-aminotransferase. l-ABA could also be produced from the reduction of α-keto acids with l-leucine dehydrogenase or glutamate dehydrogenase[1].

l?uterung methode

Crystallise butyrine from aqueous EtOH, and the melting point depends on heating rate but has m 303o in a sealed tube. [Greenstein & Winitz The Chemistry of the Amino Acids J. Wiley, Vol 3 p 2399 IR: 2401 1961, Beilstein 4 III 1294, 4 IV 2584.]

(-)-2-Aminobuttersure Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte


(-)-2-Aminobuttersure Anbieter Lieferant Produzent Hersteller Vertrieb H?ndler.

Global( 657)Lieferanten
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1492-24-6((-)-2-Aminobuttersure)Verwandte Suche:


  • L-2-AMINO-N-BUTYRIC ACID
  • L-(+)-2-AMINOBUTYRIC ACID
  • L-ALPHA-AMINO-N-BUTYRIC ACID
  • H-ABU(ALPHA)-OH
  • H-ABU(2)-OH
  • H-2-ABU-OH
  • 2-AMINO-BUTYRIC ACID
  • (S)-(+)-2-AMINO-N-BUTYRIC ACID
  • (S) 2-AMINOBUTYRIC ACID
  • (S)-(+)-2-AMINOBUTYRIC ACID
  • (S)-(+)-2-Aminobutyric acid; (S)-(+)-2-Aminobutyric acid; 2-Aminobutanoic acid;L(+)-2-Aminobutyric acid
  • H-L-NHCH(CH2CH3)-COOH
  • H-L-ABU-OH
  • (S)-(+)-α-aminobutyricacid
  • L-A-AMINO-N-BUTYRIC ACID CELL CULTURETES TED
  • L-A-AMINO-N-BUTYRIC ACID SIGMA GRADECRYS TALLINE
  • (2S)-2-Aminobutanoic Acid
  • (S)-(+)-a-2-Aminobutyric Acid
  • L-a-2-Aminobutyric Acid
  • L-Ethylglycine
  • LH-L-ABU-OH
  • L-(+)-2-Aminobutyric
  • L-2-Abu-OH
  • L-ABU-OH
  • L-2-AMINOBUTYRIC ACID >= 99% (TITRAT
  • L-α-Aminobutyric acid≥ 99% (Titration)
  • L-α-Aminobutyric acid L(+)-2-Aminobutyric acid (S)-(+)-2-Aminobutyric acid 2-Aminobutanoic acid H-Abu-OH
  • (S)-2-aminobutanoicacid
  • (s)-butanoicaci
  • Butanoic acid, 2-amino-, (S)-
  • butanoicacid,2-amino-,(S)-(+)-
  • Butyric acid, 2-amino-, L-
  • L-alpha-Aminobutyrate
  • L-Butyrine
  • L-α-aminobutyricacid
  • S-butyrine
  • H-Abu-OH (L-2-Aminobutyric acid
  • L-a-Amino-butyric acid (S)-(+)-2-Aminobutyric acid)
  • L-(+)-2-Aminobutyric acid, 98+%
  • L-α-Amino-butyric acid, L-2-Aminobutyric acid
  • H-Abu-OH (L-2-Aminobutyric acid: L-a-Amino-butyric acid: (S)-(+)-2-Aminobutyric acid)
  • H-Abu-OH (L-2-Aminobutyric acid: L-a-Amino-butyric ac:: (S)-(+)-2-Aminobutyric acid)
  • H-L-2-Abu-OH
  • L-2-Aminobutyric acid,L-α-Aminobutyric acid
  • 2-Aminobutanoic acid, TECH
  • (2S)-2-Aminobutyric acid, L-2-Aminobutyric acid
  • (S)-2-AMinobutanoic Acid, 97+%
  • L-2-Aminobutyric aCld
  • Butanoic acid, 2-amino-, (2S)-
  • NSC 97060
  • L(+)-2-AMinobutyric acid, 98% 1GR
  • D-α-aMino-n-butyric acid
  • L-2-AMinobutyric acid, (S)-(+)-2-AMinobutyric acid
  • (2S)-2-Aminobutyric acid, L-Aminobutyric acid
  • L-2-AMinobrtyric acid
  • L-Amino butanoic acid
  • Levetiracetam Impurity I
  • L-2-Abu
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