ChemicalBook >> CAS DataBase List >>Amygdalin

Amygdalin

CAS No.
29883-15-6
Chemical Name:
Amygdalin
Synonyms
D-AMYGDALIN;vitamin b17;Bitter AlMond extract;D(-)-AMYGDALIN;LAETRILE;D,L-AMYGDALIN;D-AMYGDALIN HYDRATE;(r)-alpha-((6-o-beta-d-glucopyranosyl-beta-d-glucopyranosyl)oxy)benzeneaceto;(r)-alpha-((6-o-beta-d-glucopyranosyl-beta-d-glucopyranosyl)oxy)benzeneacetonit;rile
CBNumber:
CB8363552
Molecular Formula:
C20H27NO11
Molecular Weight:
457.43
MDL Number:
MFCD00006598
MOL File:
29883-15-6.mol
MSDS File:
SDS
Last updated:2025-09-17 14:35:14

Amygdalin Properties

Melting point 223-226 °C
alpha -38.5 º (c=4, H2O)
Boiling point 563.27°C (rough estimate)
Density 1.4474 (rough estimate)
refractive index -40 ° (C=2, H2O)
storage temp. Sealed in dry,Room Temperature
solubility H2O: 0.1 g/mL hot, clear to very faintly turbid, colorless
form Powder
pka 12.69±0.70(Predicted)
color White to Off-white
biological source synthetic
optical activity [α]20/D 39±2°, c = 2% in H2O
Water Solubility 83 g/L (25 ºC)
Merck 14,597
BRN 66856
Stability Hygroscopic
InChIKey XUCIJNAGGSZNQT-SWRVSKMJSA-N
LogP -2.237 (est)
CAS DataBase Reference 29883-15-6(CAS DataBase Reference)
EWG's Food Scores 1
NCI Dictionary of Cancer Terms amygdalin; laetrile
FDA UNII 214UUQ9N0H
NCI Drug Dictionary laetrile
UNSPSC Code 41116107
NACRES NA.25

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H302
Precautionary statements  P264-P270-P301+P312-P501
Hazard Codes  Xn
Risk Statements  22
Safety Statements  26-36/37/39-45-24/25
RIDADR  2811
WGK Germany  3
RTECS  OO8450000
10-21
HazardClass  6.1(b)
PackingGroup  III
HS Code  29389090
Hazardous Substances Data 29883-15-6(Hazardous Substances Data)
Toxicity LD50 orl-rat: 522 mg/kg WJMDA2 134,97,81
NFPA 704
1
2 0

Amygdalin price More Price(53)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich PHL89559 Amygdalin phyproof® Reference Substance 29883-15-6 100 mg $268 2025-07-31 Buy
Sigma-Aldrich 10050 Amygdalin BioXtra, ≥97.0% (HPLC) 29883-15-6 5g $108 2025-07-31 Buy
Sigma-Aldrich 10050 Amygdalin BioXtra, ≥97.0% (HPLC) 29883-15-6 25g $431 2025-07-31 Buy
TCI Chemical A0443 Amygdalin >97.0%(HPLC) 29883-15-6 1g $28 2025-07-31 Buy
Cayman Chemical 26668 Amygdalin 29883-15-6 10g $68 2024-03-01 Buy
Product number Packaging Price Buy
PHL89559 100 mg $268 Buy
10050 5g $108 Buy
10050 25g $431 Buy
A0443 1g $28 Buy
26668 10g $68 Buy

Amygdalin Chemical Properties,Uses,Production

Uses and Synthetic Methods of Amygdalin

Amygdalin is a β-cyano-glycoside in the bitter almond that is bound to cyano (CN), which releases free cyano groups after eating the bitter almond, so that the food is poisoned. Amygdalin is a product of the metabolism of phenylalanine in the bitter almond. Amygdalin has β-glucosidase and amygdalinase (oxynitrilase): the former catalyzed amygdalin into two molecules of glucose and one molecule of amygdalenone through hydrolysis; the later catalyzes mandelonitrile into almond nitrile cyanide (HCN) and benzaldehyde through hydrolysis. Amygdalin exists in seeds, such as almonds.
Many plant root cells contain glycosides, with no toxic effect when in sugar type. Glycosides hydrolysis produce toxic substances leading to cell death. Mandelic glycosides contained in peach root is a glycoside. Amylose hydrolysis produce two kinds of plant toxins-hydrogen cyanide and benzaldehyde. Peeling root lesion formation and necrosis occurred in the vicinity of the stabbed nematode but not in contact zone; in addition, in vitro tests have proved that the pratylenchus penetrans can make amygdalin hydrolysis.
As a cyanide containing glucoside, it can be used as a substrate for such as maltase, almond casein and β-glucosidase identification, differentiation and characterization.

Category

Toxic substances

Toxicity classification

Highly toxic

Acute toxicity

Acute toxicity Oral-Rat LD50: 522 mg/kg; Oral-mouse LD50: 443 mg/kg

Flammability Hazardous properties

Combustible; producing toxic nitrogen oxides when heated.

Storage and transportation

Ventilation, low temperature, drying

Fire extinguishing agent

Dry powder, foam, sand, carbon dioxide

Description

Amygdalin is a cyanogenic glycoside that has been found in seeds from plants of the Rosaceae family and has diverse biological activities. It induces cell cycle arrest at the G0/G1 phase, decreases cyclin A and Cdk2 levels, and inhibits cell growth in UMUC-3, RT112, and TCCSUP bladder cancer cells when used at concentrations ranging from 1.25 to 10 mg/ml. Amygdalin (3 mg/kg) reduces the number of primary microtubules and microvessels in aortic rings isolated from rats with diabetes induced by streptozotocin . In vivo, amygdalin reduces triglyceride, total cholesterol, and LDL levels and aortic sinus plaque area in an LDLR-/- mouse model of atherosclerosis. It also reduces production of TNF-α, IL-1β, and IL-6, as well as neutrophil and macrophage infiltration, in bronchoalveolar lavage fluid (BALF) in a mouse model of LPS-induced acute lung injury.

Chemical Properties

WHITE FINE CRYSTALLINE POWDER

Uses

antiinflammatory, experimental antineoplastic

Uses

Amygdalin, a cyanide containing glycoside, may be used as a substrate to identify, differentiate and characterize enzymes such as maltase(s), emulsin(s) and β-glucosidase(s).

Uses

A cyanogenic glycoside occurring in seeds of Rosaceae, principally in bitter almonds and peach and apricot pits. Some time ago it was said to be effective in the treatment of cancer, but controlled clinical trials repeatedly failed to confirm such claims.

Definition

ChEBI: An amygdalin in which the stereocentre on the cyanohydrin function has R-configuration.

World Health Organization (WHO)

Laetrile, which consists mainly of amydgalin, a glycoside extracted from the kernels of apricots, peaches and other fruits, has been available for over 30 years in preparations purporting to be beneficial in the treatment of cancer. Although there is no evidence that these are efficacious, preparations continued to be widely used and, until the late 1970s, they were considered to be harmless. However, oral dosage forms, which may be broken down in the gut to hydrogen cyanide, have subsequently been shown to be potentially lethal. This has resulted in restrictive regulatory measures in several countries.

General Description

This substance is a primary reference substance with assigned absolute purity (considering chromatographic purity, water, residual solvents, inorganic impurities). The exact value can be found on the certificate. Produced by PhytoLab GmbH & Co. KG

Biochem/physiol Actions

Cyanogenic glycoside that is a component of bitter almonds and apricot pits. There is no scientific evidence that amygdalin itself is an effective anti-cancer agent. Recent studies using β?glucoside linked to a tumor-associated monoclonal antibody to release cyanide at the tumor cell has shown significant cytotoxicity.

Safety Profile

Human poison by ingestion(infant data). Poison experimentally by ingestion. Anexperimental teratogen. Mutation data reported. Whenheated to decomposition it emits toxic fumes of NOx.

Purification Methods

D-Amygdalin recrystallises from water as the trihydrate, or from EtOH. It is present in bitter almonds. [Smith Chem Ber 64 1115 1931, Beilstein 17/8 V 188.]

References

[1] M. FAROOQ WAHAB. Problems and Pitfalls in the Analysis of Amygdalin and Its Epimer[J]. Journal of Agricultural and Food Chemistry, 2015, 63 40: 8966-8973. DOI: 10.1021/acs.jafc.5b03120
[2] JASMINA MAKAREVI?. Amygdalin blocks bladder cancer cell growth in vitro by diminishing cyclin A and cdk2.[J]. PLoS ONE, 2014: e105590. DOI: 10.1371/journal.pone.0105590
[3] HOSSEIN MIRMIRANPOUR. Amygdalin inhibits angiogenesis in the cultured endothelial cells of diabetic rats.[J]. Indian Journal of Pathology and Microbiology, 2012, 55 2: 211-214. DOI: 10.4103/0377-4929.97874
[4] JIANZHEN LV. Amygdalin ameliorates the progression of atherosclerosis in LDL receptor?deficient mice.[J]. Molecular medicine reports, 2017: 8171-8179. DOI: 10.3892/mmr.2017.7609
[5] AO ZHANG. Protective Effect of Amygdalin on LPS-Induced Acute Lung Injury by Inhibiting NF-κB and NLRP3 Signaling Pathways.[J]. Inflammation, 2017, 40 3: 745-751. DOI: 10.1007/s10753-017-0518-4

Amygdalin Preparation Products And Raw materials

Global( 634)Suppliers
Supplier Tel Email Country ProdList Advantage
Changsha Staherb Natural Ingredients Co., Ltd.
+86-0731-84213302 +86-18374838656 info@staherb.cn China 1027 58
Hebei Chuanghai Biotechnology Co., Ltd
+8617732866630 abby@chuanghaibio.com China 8773 58
Hebei Mujin Biotechnology Co.,Ltd
+8613288715578 sales@hbmojin.com China 12338 58
Guangzhou Tengyue Chemical Co., Ltd.
+86-86-18148706580 +8618826483838 evan@tyvovo.com China 143 58
BINBO BIOLOGICAL CO.,LTD
+8618629063126 info@binbobiological.com China 453 58
Hebei Zhuanglai Chemical Trading Co.,Ltd
+8613343047651 admin@zlchemi.com China 3692 58
HEBEI SHENGSUAN CHEMICAL INDUSTRY CO.,LTD
+86-15350851019; +8615350851019 admin@86-ss.com China 999 58
Shaanxi Xianhe Biotech Co., Ltd
+86-17709210191; +8617709210191 Jerry@xhobio.com China 883 58
Wuhan JiyunZen Tech Co., Ltd.
+86-18062099985 Amyjiyunzen@yeah.net China 663 58
Henan Tianfu Chemical Co.,Ltd.
+86-0371-55170693 +86-19937530512 info@tianfuchem.com China 21622 55

Related articles

View Lastest Price from Amygdalin manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Amygdalin pictures 2025-09-17 Amygdalin
29883-15-6
US $54.00 / mg 100.00% 10g TargetMol Chemicals Inc.
Amygdalin pictures 2025-09-17 Amygdalin
29883-15-6
US $0.00-0.00 / Kg/Drum 1KG 98%min HPLC 500kgs WUHAN FORTUNA CHEMICAL CO., LTD
Amygdalin pictures 2025-09-17 Amygdalin
29883-15-6
US $5.00-0.50 / KG 0.10000000149011612KG 99% hplc 5000kg Wuhan JiyunZen Tech Co., Ltd.
  • Amygdalin pictures
  • Amygdalin
    29883-15-6
  • US $54.00 / mg
  • 100.00%
  • TargetMol Chemicals Inc.
  • Amygdalin pictures
  • Amygdalin
    29883-15-6
  • US $0.00-0.00 / Kg/Drum
  • 98%min HPLC
  • WUHAN FORTUNA CHEMICAL CO., LTD
  • Amygdalin pictures
  • Amygdalin
    29883-15-6
  • US $5.00-0.50 / KG
  • 99% hplc
  • Wuhan JiyunZen Tech Co., Ltd.
(r)-alpha-((6-o-beta-d-glucopyranosyl-beta-d-glucopyranosyl)oxy)benzeneaceto (r)-alpha-((6-o-beta-d-glucopyranosyl-beta-d-glucopyranosyl)oxy)benzeneacetonit (r)-oxy) (r)-y) amygdaloside benzeneacetonitrile,alpha-((6-o-beta-d-glucopyranosyl-beta-d-glucopyranosyl) benzeneacetonitrile,alpha-((6-o-beta-d-glucopyranosyl-beta-d-glucopyranosyl)ox Amygdalin 29883-15-6 2-(hydroxymethyl)-6-[[3,4,5-trihydroxy-6-(methoxymethyl)-2-oxanyl]methoxymethyl]oxane-3,4,5-triol D(-)-Amygdalin hydrate,95% [(6-O-Hexopyranosylhexopyranosyl)-oxy](phenyl)-acetonitrile AMYGDALIN 6-O-BETA-D-GLUCOSIDO-BETA-D-GLUCOSIDE d(-)-mandelonitrile-beta-d-gentiobioside mandelonitrile-beta-gentiobioside nsc-15780 rile BENZENEACETONITRILE-[(6-O-BETA-D-GLUCOPYRANOSYL-BETA-D-GLUCOPYRANOSYL)OXY]-, (R)- D(-)-AMYGDALIN D-AMYGDALIN D-AMYGDALIN HYDRATE D-MANDELONITRILE 6-O-BETA-D-GLUCOSIDO-BETA-D-GLUCOSIDE D-MANDELONITRILE 6-O-BETA-D-GLUCOSIDO-BETA-D-GLUCOSIDE D-MANDELONITRILE BETA-GENTIOBIOSIDE D-MANDELONITRILE-BETA-D-GLUCOSIDO-6-BETA-D-GLUCOSIDE D-MANDELONITRILE-BETA-GENTIOBIOSIDE GLUCOPRUNASIN LAETRILE MANDELONITRILE GENTIOBIOSIDE Amygdalin,D-Mandelonitrile 6-O-β-D-glucosido-β-D-glucoside, D-Mandelonitrile-β-gentiobioside, Laetrile D-Amygdalin, 98+% D-Amygdalin,D-Mandelonitrile β-gentiobioside, D-Mandelonitrile 6-O-β-D-glucosido-β-D-glucoside, D-Mandelonitrile-β-gentiobioside, Amygdalin, Laetrile D-Mandelonitrile-β-gentiobioside ,98% Benzeneacetonitrile,alpha-((6-o-beta-d-glucopyranosyl-beta-d-glucopyr AMygdalin(VitaMin B17 AMygdaloside (disaccharide) Nitrilosides (R)-2-phenyl-2-(((2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-((((2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxyMethyl)tetrahydro-2H-pyran-2-yl)oxy)Methyl)tetrahydro-2H-pyran-2-yl)oxy)acetonitrile AMygdalin /VB17/Laetrile AMygdalin /VB17/Laetril Bitter AlMond extract D-Mandelonitrile 6-O-β-D-glucosido-β-D-glucoside D-Mandelonitrile-β-gentiobioside Mygdalin D-AMYGDALIN FROM APRICOT KERNELS AMYGDALIN: BENZENEACETONITRILE,-[(6-O--D-GLUCOPYRANOSYL--D-GLUCOPYRANOSYL)OXY]-, (R)- D-Amygdalin (1.12428) D-Amygdalinhydrate,96% Benzeneacetonitrile, .alpha.-(6-O-.beta.-D-glucopyranosyl-.beta.-D-glucopyranosyl)oxy-, (.alpha.R)- d-mandelonitrile-á-d-glucosido-6-á-d-glucoside vitamin b17 D-Mandelonitrile-b-gentiobioside AMYGDALIN(RG) D,L-AMYGDALIN (2R)-2-Phenyl-2-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxyacetonitrile (R)-Amygdalin (R)-Amygdaloside (R)-Laenitrile AMYGDALIN BIOXTRA, >= 97.0% (HPLC)