1-Aminocyclopropanecarboxylic acid - ≥98% , CAS No.22059-21-8

CAS: 22059-21-8 Cat. No.: A101238 Molecular Weight: 101.1 Beilstein Registry Number: 2076413 EC Number: 606-917-8
AVAILABLE TO ORDER
GRADE & PURITY ≥98%
Synonyms
1-amino-cyclopropane-1-carboxylic acid | 1-Aminocyclopropane-1-carboxylic acid | BBL100145 | HY-30004 | Spectrum3_001515 | 1-aminocyclopropane-1-carboxylate | alpha-Aminocyclopropane carboxylic acid | AM20090214 | 1y20 | Spectrum5_001755 | Cyclopropanecar
Storage
Argon charged,Room temperature
Shipped In
Normal
 ·  off list, applied to all prices below.
Size
Status
Price
Qty
1g
A101238-1g
3
$9.90
5g
A101238-5g
3
$19.90
25g
A101238-25g
2
$47.90
100g
A101238-100g
2
$169.90
500g
A101238-500g
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.
$625.90
Enter a quantity for the sizes you want to add.
🧪

Why this grade

≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Argon charged,Room temperature Ships Normal Check lot-specific COA for exact specifications.

📋

Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 3 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Overview

Application

1-Aminocyclopropane-1-carboxylic Acid is an intermediate in the conversion of methionine to ethylene during the ripening in apples. It also plays an important role in the biosynthesis of the plant hormone ethylene.1-Aminocyclopropane-1-carboxylic Acid is shown to block convulsions and death produced by NMDA exposure, significantly reducing seizure induction and cell death of NMDA-treated hippocampal neurons. 1-Aminocyclopropane-1-carboxylic Acid is produced endogenously in the tomato and other higher plants as a product of the action of 1-aminocyclopropane-1-carboxylic acid synthase in the biosynthesis of ethylene.

Specifications

Synonyms
1-amino-cyclopropane-1-carboxylic acid | 1-Aminocyclopropane-1-carboxylic acid | BBL100145 | HY-30004 | Spectrum3_001515 | 1-aminocyclopropane-1-carboxylate | alpha-Aminocyclopropane carboxylic acid | AM20090214 | 1y20 | Spectrum5_001755 | Cyclopropanecar
Specifications & Purity
≥98%
Biochemical and Physiological Mechanisms
NMDA agonist acting at the glycine site 1-Aminocyclopropanecarboxylic acid (ACC) exhibits anticonvulsant, anxiolytic, anti-addictive, neuroprotective and antidepressant-like effects in rats and mice. ACC does not affect memory or learning processes.
Storage
Argon charged, Room temperature
Shipped In
Normal
Note
Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.
Purity
≥98%
Names and Identifiers
Pubchem Sid504750394
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504750394
Canonical SmilesC1CC1(C(=O)O)N
IUPAC Name1-aminocyclopropane-1-carboxylic acid
InChIKeyPAJPWUMXBYXFCZ-UHFFFAOYSA-N
INCHI1S/C4H7NO2/c5-4(1-2-4)3(6)7/h1-2,5H2,(H,6,7)
Isomeric SMILES C1CC1(C(=O)O)N
WGK Germany 3
RTECS GZ1110000
Molecular Weight 101.1
Beilstein 2076413
Reaxy-Rn 2076413
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2076413&ln=

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganic acids and derivatives
ClassCarboxylic acids and derivatives
SubclassAmino acids, peptides, and analogues
Intermediate Tree Nodes Amino acids and derivatives - Alpha amino acids and derivatives
Direct ParentAlpha amino acids
Alternative Parents 1-aminocyclopropane-1-carboxylic acids and derivatives  Cyclopropanecarboxylic acids  Amino acids  Monocarboxylic acids and derivatives  Carboxylic acids  Organopnictogen compounds  Organic oxides  Monoalkylamines  Hydrocarbon derivatives  Carbonyl compounds  
Molecular FrameworkAliphatic homomonocyclic compounds
Substituents Alpha-amino acid - 1-aminocyclopropane-1-carboxylic acid or derivatives - Cyclopropanecarboxylic acid - Cyclopropanecarboxylic acid or derivatives - Amino acid - Carboxylic acid - Monocarboxylic acid or derivatives - Organic nitrogen compound - Organooxygen compound - Organonitrogen compound - Primary amine - Primary aliphatic amine - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Carbonyl group - Amine - Organic oxygen compound - Aliphatic homomonocyclic compound
DescriptionThis compound belongs to the class of organic compounds known as alpha amino acids. These are amino acids in which the amino group is attached to the carbon atom immediately adjacent to the carboxylate group (alpha carbon).
External Descriptors monocarboxylic acid - non-proteinogenic alpha-amino acid
3D Structure
Interactive Chemical Structure Model





Associated Targets(Human)
CHRM1 Tclin Muscarinic acetylcholine receptor M1 (12690 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
TSHR Tclin Thyroid stimulating hormone receptor (29986 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP2D6 Tclin Cytochrome P450 2D6 (33882 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP1A2 Tchem Cytochrome P450 1A2 (26471 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP2C9 Tchem Cytochrome P450 2C9 (32119 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP2C19 Tchem Cytochrome P450 2C19 (29246 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP3A4 Tclin Cytochrome P450 3A4 (53859 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
EHMT2 Tchem Histone-lysine N-methyltransferase, H3 lysine-9 specific 3 (93046 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLCO1B1 Tchem Solute carrier organic anion transporter family member 1B1 (2672 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CBX1 Tbio Chromobox protein homolog 1 (92434 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLCO1B3 Tchem Solute carrier organic anion transporter family member 1B3 (2517 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Associated Targets(non-human)
Hdac6 Histone deacetylase 6 (222 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Saccharomyces cerevisiae (19171 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mus musculus (284745 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
rep Replicase polyprotein 1ab (378 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
pfk 6-phospho-1-fructokinase (7870 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ffp 4'-phosphopantetheinyl transferase ffp (24982 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Grin1 Glutamate NMDA receptor (6467 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Slc1a5 Amino acid transporter (271 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mechanisms of Action
Certificates(CoA,COO,BSE/TSE and Analysis Chart)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

27 results found

Lot NumberCertificate TypeDateItem
I2209109Certificate of AnalysisJun 11, 2026 A101238
C2212146Certificate of AnalysisDec 10, 2025 A101238
G2502529Certificate of AnalysisJul 04, 2025 A101238
B2625190Certificate of AnalysisJun 25, 2025 A101238
H2529136Certificate of AnalysisJun 25, 2025 A101238
H2529135Certificate of AnalysisJun 25, 2025 A101238
H2529134Certificate of AnalysisJun 25, 2025 A101238
H2529133Certificate of AnalysisJun 25, 2025 A101238
H2529132Certificate of AnalysisJun 25, 2025 A101238
A2607092Certificate of AnalysisJun 25, 2025 A101238
F2425074Certificate of AnalysisApr 02, 2024 A101238
F2425077Certificate of AnalysisApr 02, 2024 A101238
F2425076Certificate of AnalysisApr 02, 2024 A101238
F2425075Certificate of AnalysisApr 02, 2024 A101238
K1520059Certificate of AnalysisJul 10, 2023 A101238
C1519001Certificate of AnalysisDec 09, 2022 A101238
I2209143Certificate of AnalysisJul 20, 2022 A101238
I2209112Certificate of AnalysisJul 20, 2022 A101238
I2209146Certificate of AnalysisJul 20, 2022 A101238
I2209349Certificate of AnalysisJul 20, 2022 A101238
L2305169Certificate of AnalysisJul 20, 2022 A101238
G2403014Certificate of AnalysisJul 20, 2022 A101238
F2526062Certificate of AnalysisJul 20, 2022 A101238
C2513182Certificate of AnalysisJul 20, 2022 A101238
C2212175Certificate of AnalysisJan 24, 2022 A101238
C2212174Certificate of AnalysisJan 24, 2022 A101238
C2212145Certificate of AnalysisJan 24, 2022 A101238

Show more ⌵

Chemical and Physical Properties
SolubilitySoluble in water.
SensitivityMoisture sensitive.
Melt Point(°C)229-231°C
Molecular Weight101.100 g/mol
XLogP3-2.800
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count3
Rotatable Bond Count1
Exact Mass101.048 Da
Monoisotopic Mass101.048 Da
Topological Polar Surface Area63.300 Ų
Heavy Atom Count7
Formal Charge0
Complexity106.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Documents & Articles
Citations of This Product
References
1. Cai Zeping, Dai Yinuo, Jin Xia, Xu Hui, Huang Zhen, Xie Zhenyu, Yu Xudong, Luo Jiajia.  (2024)  Ambient temperature regulates root circumnutation in rice through the ethylene pathway: transcriptome analysis reveals key genes involved.  Frontiers in Plant Science,      [PMID:38525142] [10.3389/fpls.2024.1348295]
2. Guannan Kong, Da Song, Chao Zhang, Xinyao Jia, Yingying Ren, Shuhe Wei, Huiping Dai.  (2025)  The Effect of Plant Growth Promoting Rhizobacteria Bacillus thuringiensis LKT25 on Cadmium Accumulation and Physiological Responses in Solanum nigrum L..  Plants-Basel,  14  (18): (2918).  [PMID:41012069] [10.3390/plants14182918]
3. Liu Yitong, Liu Shuangrong, Jing Yanjun, Li Jialong, Lin Rongcheng.  (2025)  Light regulates seed dormancy through FHY3-mediated activation of ACC OXIDASE 1 in Arabidopsis.  PLANT MOLECULAR BIOLOGY,  115  (2): (1-13).  [PMID:40082285] [10.1007/s11103-025-01559-9]
Solution Calculators
Reviews

Customer Reviews

Shall we send you a message when we have discounts available?

Remind me later

Thank you! Please check your email inbox to confirm.

Oops! Notifications are disabled.