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Avermectin B1a

CAS No.
65195-55-3
Chemical Name:
Avermectin B1a
Synonyms
Abamectina;Avamectin B1a;AbaMectin B1a;C-076B1a;ABERMECTINS;Abamectinum;avermectin b1a;Antibiotic C-076B1a;Abamectine [french];Abamectinum [latin]
CBNumber:
CB5854808
Molecular Formula:
C48H72O14
Molecular Weight:
873.09
MDL Number:
MFCD01939385
MOL File:
65195-55-3.mol
Last updated:2023-06-08 09:02:51

Avermectin B1a Properties

Boiling point 940.9±65.0 °C(Predicted)
Density 1.24±0.1 g/cm3(Predicted)
storage temp. Store at -20°C
solubility ≥143.4 mg/mL in DMSO; ≥11.86 mg/mL in EtOH with ultrasonic; insoluble in H2O
form Powder
pka 12.42±0.70(Predicted)
Stability Hygroscopic
FDA UNII K54ZMM929K
EPA Substance Registry System Avermectin B1a (65195-55-3)

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictogramsGHS hazard pictogramsGHS hazard pictograms
GHS08,GHS09,GHS06
Signal word  Danger
Hazard statements  H330-H410-H300-H361d-H372
Precautionary statements  P273-P391-P501-P260-P271-P284-P304+P340-P310-P320-P403+P233-P405-P501-P260-P264-P270-P314-P501-P264-P270-P301+P310-P321-P330-P405-P501
RIDADR  2588
HazardClass  6.1(a)
PackingGroup  II
Toxicity LD20 orl-rat: 10 mg/kg JAFCAU 32,94,84
NFPA 704
0
4 0

Avermectin B1a price More Price(21)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Cayman Chemical 22000 Avermectin B1a ≥99% 65195-55-3 5mg $152 2024-03-01 Buy
Cayman Chemical 22000 Avermectin B1a ≥99% 65195-55-3 25mg $735 2021-12-16 Buy
Cayman Chemical 22000 Avermectin B1a 65195-55-3 1mg $68 2024-03-01 Buy
Cayman Chemical 22000 Avermectin B1a 65195-55-3 10mg $368 2021-12-16 Buy
Usbiological A4447 Avermectin B1a 65195-55-3 1mg $503 2021-12-16 Buy
Product number Packaging Price Buy
22000 5mg $152 Buy
22000 25mg $735 Buy
22000 1mg $68 Buy
22000 10mg $368 Buy
A4447 1mg $503 Buy

Avermectin B1a Chemical Properties,Uses,Production

Description

Avermectin B1a is a macrocyclic lactone disaccharide anthelmintic agent that binds to high and low affinity sites on the mammalian GABAA receptor. Binding to the high affinity site activates the receptor to increase chloride influx, while binding to the low affinity site blocks the channel. Avermectin B1a inhibits binding of the glycine receptor antagonist strychnine to membranes and the solubilized receptor from rat spinal cord (Kis = 1.3 and 3.6 μM, respectively). Formulations containing avermectin B1a (>80%) and avermectin B1b (~20%; ) are used in insecticides and veterinary anthelmintic formulas as abamectin .

Originator

Abamectin,Yellow River Enterprise Co. (a.k.a Yelori)

Uses

Avermectin B1a is the major component (>80%) of a commercially available anthelmintic used to control parasitic nematodes in livestock. Avermectin B1a contains a secbutyl residue in the 25-position. In vitro and in vivo studies have shown that this analogue is the more potent analogue in the commercial product.

Definition

ChEBI: Avermectin B1a is an avermectin.

Manufacturing Process

1. The contents of a lyophilized tube of Streptomyces avermitilis MA-4680 is transferred aseptically to a 250 ml Erlenmeyer flask containing 305 ml of Medium 1: Dextrose 20 g, Peptone 5 g, Meat Extract 5 g, Primary Yeast 3 g, NaCl 5 g, CaCO3 (after pH adjustment) 3 g, Distilled water 1000 ml, pH 7.0. The inoculated flask is incubated for 3 days at 28°C on a rotary shaking machine at a speed of 220 RPM in a 2 inch radius circular orbit. At the end of this time, a 250 ml Erlenmeyer flask containing 50 ml of Medium 2 [Tomato Paste 20 g, Modified Starch (CPC) 20 g, Primary Yeast 10 g, CoCl2·6H2O 0.005 g, Distilled water 1000 ml, pH 7.2-7.4] is inoculated with a 2 ml sample from the first flask. This flask is incubated for 3 days at 28°C on a rotary shaking machine at a speed of 220 RPM in a 2 inch diameter circular orbit. 50 Ml of the resulting fermentation broth containing C-076 is effective against an N.dubius infection in mice.
2. A lyophilized tube of Streptomyces avermitilis MA-4680 is opened aseptically and the contents suspended in 50 ml of Medium 1 in a 250 ml Erlenmeyer flask. This flask is shaken for 3 days at 28°C on a rotary shaking machine 220 RPM with a 2 inch diameter circular orbit. A 0.2 ml portion of this seed medium is used to inoculate a Slant of Medium 3: Dextrose 10.0 g , Bacto Asparagine 0.5 g, K2HPO4 40.5 g, Bacto Agar 15.0 g , Distilled water 1000 ml, pH 7.0. The inoculated slant medium is incubated at 28°C for 10 days and stored at 4°C until used to inoculate 4 more slants of Medium 3. These slants are incubated in the dark for 8 days. One of these slants is used to inoculate 3 baffled 250 ml Erlenmeyer flasks containing 50 ml of No. 4 Seed Medium: Soluble Starch 10.0 g, Ardamine 5.0 g, NZ Amine E 5.0 g, Beef Extract 3.0 g, MgSO4·7H2O 0.5 g, Cerelose 1.0 g, Na2HPO4 0.190 g, KH2PO4 182 g, CaCO3 0.5 g, Distilled water 1000 ml, pH 7.0-7.2. The seed flasks are shaken for 2 days at 27-28°C on a rotary shaking machine at 220 RPM with a 2 inch diameter circular orbit. The contents of these flasks are pooled and used to inoculate (5% inoculum) baffled 250 ml Erlenmeyer flasks containing 40 ml of various production media. Flasks containing media 2, 5 and 6 are incubated for 4 days at 28°C on a rotary shaking machine at 220 RPM with a 2 inch diameter circular orbit. The resulting broth containing C-076 is then harvested and tested for anthelmintic activity. In all cases 6.2 ml of whole broth and the solids obtained from centrifuging 25 ml of whole broth are fully active against N.dubius helminth infections in mice.
3. The one of the four slants of Medium 3 prepared as in Example 2 is used to inoculate a baffled 250 ml Erlenmeyer flask containing 50 ml of Seed Medium No. 4. The seed flask is shaken for 1 day at 27- 28°C on a rotary shaking machine at 220 RPM with a 2 inch diameter circular orbit. The seed flask is then stored stationary at 4°C until it is ready to be used. The contents of this flask are then used to inoculate (5% inoculum) 20 unbaffled 250 ml Erlenmeyer flasks containing 40 ml of Medium No. 2. After 4 days incubation at 28°C on a rotary shaking machine at 220 RPM with a 2 inch diameter circular orbit, 19 of the flasks are harvested and pooled. The combined fermentation broths containing C-076 are filtered affording 500 ml of filtrate and 84 g of mycelia. 78 G of mycelia are extracted with 150 ml of acetone for ? hour with stirring and the mixture filtered. The filter cake is washed with 50 ml of acetone and the filtrate and washings are combined and concentrated to 46.5 ml 30 Ml of the concentrate is adjusted to pH 4 with dilute hydrochloric acid and extracted 3 times with 30 ml portions of chloroform. The extracts are dried by filtering through dry Infusorial Earth (Super-Cel) combined and concentrated to dryness in vacuum. The oily residue of C-076 weighing 91.4 mg is dissolved in chloroform sufficient to make 3 ml of solution which represents 1% of broth volume. The C-076 (Abamectin) obtained in this recovery procedure is fully active against N.dubius infections in mice. In addition, the chloroform extraction achieved a 70 fold purification of C-076 from the whole broth.

brand name

(Merck)Avomec [Veterinary] (Merial); Bovitin [Veterinary] (Merial); Doratect [Veterinary] (Merial); Duomectin [Veterinary] (Merial); Duotin [Veterinary] (Merial); Endecto (Merck); Enzec (Merck); Enzek (Merck); Parafoil (Merck); Vertimil (Zectin (Merck).

Therapeutic Function

Antiparasitic

Hazard

A poison by ingestion. Moderately toxic by skin contact.

Safety Profile

A poison by ingestion.Moderately toxic by skin contact. When heated todecomposition it emits acrid smoke and irritating fumes.

target

insect

87319-04-8
65195-55-3
Synthesis of Avermectin B1a from Ethanamine, N-[(3,5-dichlorophenyl)methylene]-2,2-diethoxy-

Avermectin B1a Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 155)Suppliers
Supplier Tel Email Country ProdList Advantage
Henan Tianfu Chemical Co.,Ltd.
+86-0371-55170693 +86-19937530512 info@tianfuchem.com China 21689 55
Hefei TNJ Chemical Industry Co.,Ltd.
+86-0551-65418679 +86-18949832763 info@tnjchem.com China 2989 55
Hubei xin bonus chemical co. LTD
86-13657291602 linda@hubeijusheng.com CHINA 22968 58
Standardpharm Co. Ltd.
86-714-3992388 overseasales1@yongstandards.com United States 14336 58
Chongqing Chemdad Co., Ltd
+86-023-61398051 +8613650506873 sales@chemdad.com China 39916 58
career henan chemical co
+86-0371-86658258 15093356674; factory@coreychem.com China 29826 58
Shaanxi Dideu Medichem Co. Ltd
+86-29-87569266 15319487004 1015@dideu.com China 2263 58
SIMAGCHEM CORP
+86-13806087780 sale@simagchem.com China 17367 58
Shanghai UCHEM Inc.
+862156762820 +86-13564624040 sales@myuchem.com China 6708 58
BOC Sciences
+16314854226 inquiry@bocsci.com United States 19743 58

View Lastest Price from Avermectin B1a manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Avermectin B1a pictures 2020-04-28 Avermectin B1a
65195-55-3
US $0.00-0.00 / KG 1KG 99.0% 500 tons Shaanxi Dideu Medichem Co. Ltd
Avermectin B1a pictures 2020-01-09 Avermectin B1a
65195-55-3
US $1.00 / KG 1KG 98% HPLC 10 tons/month Career Henan Chemical Co
  • Avermectin B1a pictures
  • Avermectin B1a
    65195-55-3
  • US $0.00-0.00 / KG
  • 99.0%
  • Shaanxi Dideu Medichem Co. Ltd
  • Avermectin B1a pictures
  • Avermectin B1a
    65195-55-3
  • US $1.00 / KG
  • 98% HPLC
  • Career Henan Chemical Co

Avermectin B1a Spectrum

avermectin b1a ABAMECTIN BETA-CYPERMETHRIN 1% ABERMECTINS AverMectin A1a,5-O-deMethyl- 5-o-demethyl-avermectin a1 5-O-DemethylAvermectin A1a Antibiotic C-076B1a C-076B1a Abamectin component B1a Abamectin komponente B1a Abamectina [spanish] Abamectine [french] Abamectinum Abamectinum [latin] AverMectin B1a (AbaMectin B1a) 5-O-DeMethylaverMectin A1a, C 076B1a. Ivermectin Impurity 1(Ivermectin EP Impurity A) Ivermectin EP Impurity A (Avermectin B1a) Ivermectin EP Impurity A (Avermectin B1a) (Abamectin B1a) Avamectin B1a Abamectina AbaMectin B1a Ivermectin impurity 2 Avermectin B1a Impurity / Avermectin Impurity-A vermectin B1a, EvoPure? 65195-55-3 C47H72O14