(S)-(+)-Methyl mandelate

Product Name: (S)-(+)-Methyl mandelate
CAS No.: 21210-43-5
Chemical Name: (S)-(+)-Methyl mandelate
Synonyms: METHYL L-(+)-MANDELATE;(+)-METHYL L-MANDELATE;METHYL (S)-(+)-MANDELATE;(S)-(+)-METHYL MANDELATE;MethylL-(+)-Mandelate>S-Plus-mandelic acid methyl;(S)-MANDELIC ACID METHYL ESTER;METHYL (S)-(+)-MANDELATE, 99+%;(S)-(+)-Methyl mandelate, 98+%;Methyl (S)-(+)-mandelate, >=98%
CBNumber: CB5345322
Molecular Formula: C9H10O3
Formula Weight: 166.17
MOL File: 21210-43-5.mol

More

Less

(S)-(+)-Methyl mandelate Property

Melting point:: 56-58 °C
Boiling point:: 138 °C / 16mmHg
alpha: 142 º (c=2, MeOH)
Density: 1.1097 (rough estimate)
refractive index: 1.4371 (estimate)
Flash point:: >110°C
storage temp.: Sealed in dry,Room Temperature
solubility: Chloroform (Sparingly), Methanol (Sparingly)
form: Solid
pka: 12.19±0.20(Predicted)
color: White to Off-White
optical activity: [α]20/D +144°, c = 1 in methanol
BRN: 2614741
InChIKey: ITATYELQCJRCCK-QMMMGPOBSA-N
CAS DataBase Reference: 21210-43-5(CAS DataBase Reference)

More

Less

Safety

Safety Statements: 22-24/25
WGK Germany: 3
HS Code: 29181990

More

Less

Hazard and Precautionary Statements (GHS)

More

Less

N-Bromosuccinimide Price

Sigma-Aldrich

Product number: 251542
Product name: Methyl (S)-(+)-mandelate
Purity: ≥99%
Packaging: 5g
Price: $70
Updated: 2023/01/07

TCI Chemical

Product number: M1350
Product name: Methyl L-(+)-Mandelate
Purity: >98.0%(GC)
Packaging: 1g
Price: $19
Updated: 2024/03/01

TCI Chemical

Product number: M1350
Product name: Methyl L-(+)-Mandelate
Purity: >98.0%(GC)
Packaging: 5g
Price: $23
Updated: 2024/03/01

Alfa Aesar

Product number: L14070
Product name: Methyl (S)-(+)-mandelate, 99%
Packaging: 1g
Price: $28.8
Updated: 2021/12/16

TRC

Product number: M317450
Product name: Methyl (S)-(+)-mandelate
Packaging: 5g
Price: $70
Updated: 2021/12/16

More

Less

(S)-(+)-Methyl mandelate Chemical Properties,Usage,Production

Chemical Properties

white crystalline powder

Uses

Methyl (S)-(+)-Mandelate (cas# 21210-43-5) is a compound useful in organic synthesis.

Uses

Methyl (S)-(+)-mandelate may be used in the preparation of (S)-(-)2-hydroxy-1,2,2-triphenylethyl acetate and (α′S)-α′-methoxycarbonylbenzyl (2S,4R)-(+)-1,2,4,5-tetrahydro-4-methyl-7,8-methylenedioxy-5-oxo-3-benzothiepin-2-carboxylate.

General Description

Optically active building block.

(S)-(+)-Methyl mandelate Preparation Products And Raw materials

Raw materials

Sodium chloride Chloroform (S)-(+)-Mandelic acid Methanol Magnesium sulfate Thionyl chloride

Preparation Products

More

Less

(S)-(+)-Methyl mandelate Suppliers

Americas 1 Belgium 1 Canada 2 China 137 Europe 1 France 1 Germany 2 India 7 Japan 4 South Korea 1 Switzerland 3 United Kingdom 3 United States 22 Global 185

Accela ChemBio Inc.

Tel: +1(858) 699-3322
Fax: +1(858) 876-1948
Email: marketing@accelachem.com
Country: United States
ProdList: 6024
Advantage: 65

Alchem Pharmtech,Inc.

Tel: 8485655694
Email: sales@alchempharmtech.com
Country: United States
ProdList: 63687
Advantage: 58

Aladdin Scientific

Tel: +1-+1(833)-552-7181
Email: sales@aladdinsci.com
Country: United States
ProdList: 57505
Advantage: 58

United States Biological

Tel: --
Fax: --
Email: sales@advtechind.com
Country: United States
ProdList: 6075
Advantage: 58

Frontier Scientific Services, Inc.

Tel: --
Fax: --
Email: customerservice@frontierssi.com
Country: United States
ProdList: 1575
Advantage: 0

United States Biological

Tel: --
Fax: --
Email: chemicals@usbio.net
Country: United States
ProdList: 6214
Advantage: 80

Combi-Blocks Inc.

Tel: --
Fax: --
Email: sales@combi-blocks.com
Country: United States
ProdList: 6618
Advantage: 69

Riedel-de Haen AG

Tel: --
Fax: --
Country: United States
ProdList: 6773
Advantage: 87

TCI America

Tel: --
Fax: --
Email: sales@tciamerica.com
Country: United States
ProdList: 6909
Advantage: 75

Frontier Scientific, Inc.

Tel: --
Fax: --
Email: sales@frontiersci.com
Country: United States
ProdList: 6222
Advantage: 86

Matrix Scientific

Tel: --
Fax: --
Email: sales@matrixscientific.com
Country: United States
ProdList: 6632
Advantage: 80

Waterstone Technology, LLC

Tel: --
Fax: --
Email: sales@waterstonetech.com
Country: United States
ProdList: 6786
Advantage: 30

Alfa Aesar

Tel: --
Fax: --
Email: tech@alfa.com
Country: United States
ProdList: 6814
Advantage: 81

Chem-Impex International, Inc.

Tel: --
Fax: --
Country: United States
ProdList: 6730
Advantage: 64

Advance Scientific & Chemical

Tel: --
Fax: --
Email: sales@advance-scientific.com
Country: United States
ProdList: 6419
Advantage: 71

3B Scientific Corporation

Tel: --
Fax: --
Email: sales@3bsc.com
Country: United States
ProdList: 6718
Advantage: 47

AK Scientific, Inc.

Tel: --
Fax: --
Email: sales@aksci.com
Country: United States
ProdList: 6347
Advantage: 65

Chemiplus Corporation

Tel: --
Fax: --
Email: okazaki@chemiplus.com
Country: United States
ProdList: 3198
Advantage: 38

Sciencelab.com, Inc.

Tel: --
Fax: --
Email: accounting@sciencelab.com
Country: United States
ProdList: 4159
Advantage: 82

ASDI Incorporated

Tel: --
Fax: --
Email: customerservice@asdi.net
Country: United States
ProdList: 6922
Advantage: 67

Advanced Asymmetrics, Inc.

Tel: --
Fax: --
Email: sales@advancedasymmetrics.com
Country: United States
ProdList: 521
Advantage: 42

Spectrum Chemicals & Laboratory Products

Tel: --
Fax: --
Email: sales@spectrumchemical.com
Country: United States
ProdList: 6699
Advantage: 77

More

Less

View Lastest Price from (S)-(+)-Methyl mandelate manufacturers

Honest Joy Holdings Limited

Product: (S)-(+)-Methyl mandelate 21210-43-5
Price: US $0.00/KG
Min. Order: 1KG
Purity: 99.1%
Supply Ability: 100 tons
Release date: 2022-01-26

Zhuozhou Wenxi import and Export Co., Ltd

Product: (S)-(+)-Methyl mandelate 21210-43-5
Price: US $15.00-10.00/KG
Min. Order: 1KG
Purity: 99%+ HPLC
Supply Ability: Monthly supply of 1 ton
Release date: 2021-07-11

Zhuozhou Wenxi import and Export Co., Ltd

Product: (S)-(+)-Methyl mandelate 21210-43-5
Price: US $15.00-10.00/KG
Min. Order: 1KG
Purity: 99%+ HPLC
Supply Ability: Monthly supply of 1 ton
Release date: 2021-07-09

21210-43-5, (S)-(+)-Methyl mandelateRelated Search:

Methyl benzoate FATTY ACID METHYL ESTER MIX C8-C22 Methylparaben Mandelic acid Methyl methacrylate Methyl formate (S)-(+)-Mandelic acid Thiophanate-methyl Methyl acetate Methyl acrylate METSULFURON METHYL Methyl salicylate Bensulfuron methyl Kresoxim-methyl Methyl Parathion-methyl Methyl bromide DL-METHYL MANDELATE,(+/-)-METHYL MANDELATE,METHYL MANDELATE

METHYL (S)-(+)-MANDELATE

(+)-METHYL (S)-ALPHA-HYDROXY-PHENYL ACETATE

METHYL (S)-ALPHA-HYDROXYPHENYLACETATE

(+)-METHYL L-MANDELATE

METHYL L-(+)-MANDELATE

(+)-L-MANDELIC ACID METHYL ESTER

L-(+)-MANDELIC ACID METHYL ESTER

S-Plus-mandelic acid methyl

Methyl (<i>S</i>)-(+)-mandelate

Methyl (S)-(+)-mandelate, >=98%

L-Mandelic Acid Methyl Ester,99%e.e.

(S)-(+)-METHYL MANDELATE

(S)-MANDELIC ACID METHYL ESTER

METHYL (S)-(+)-MANDELATE, 99+%

(S)-(+)-alpha-Hydroxyphenylaceticacidmethylester~(S)-(+)-Mandelicacidmethylester

(S)-(+)-ALPHA-HYDROXYPHENYLACETIC ACID METHYL ESTER

(S)-(+)-Methyl mandelate, 98+%

Benzeneacetic acid, .alpha.-hydroxy-, methyl ester, (.alpha.S)-

(+)-methyl (s)-α-hydroxy-phenyl acetate

(+)-methyl (s)-α-hydroxy-phenylacetate

(s)-(+)-à-hydroxyphenylacetic acid methyl ester

(+)-Methyl (S)-alpha-hydroxyphenylacetate

(S)-Methyl 2-hydroxy-2-phenylacetate ,98%

(S)-2-Hydroxy-2-phenylacetic acid methyl ester

(S)-Phenyl(hydroxy)acetic acid methyl ester

(S)-Phenylhydroxyacetic acid methyl ester

[S,(+)]-Phenylglycolic acid methyl ester

[S,(+)]-α-Hydroxybenzeneacetic acid methyl ester

(+)-Methyl (S)-α-hydroxy-phenylacetate, S(+)-Mandelic acid methyl ester

(+)-Methyl (S)-α-hydroxyphenylacetate, (+)-Methyl L-mandelate

(S)-Methyl 2-hydroxy-2-phenylacetate

Methyl (S)-2-Hydroxy-2-phenylacetate

Methyl (S)-α-Hydroxybenzeneacetate

MethylL-(+)-Mandelate&gt

Benzeneacetic acid, α-hydroxy-, methyl ester, (αS)-

(S)-(+)-Methyl mandelate ISO 9001：2015 REACH

Methyl (2S)-hydroxy(phenyl)acetate

21210-43-5

C6H5CHOHCO2CH3

Chiral Resolving Reagents

Chiral Resolution Reagents

Asymmetric Synthesis

Chiral Building Blocks

Esters (Chiral)

Aromatics

Chiral Reagents

Chiral Building Blocks

Esters (Chiral)

Synthetic Organic Chemistry

Chiral Compound