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367559

(S)-(+)-1-Aminoethylphosphonic acid

Name: (<I>S</I>)-(+)-1-Aminoethylphosphonic acid
Brand: ALDRICH

99%

Synonym(s):

D-(+)-1-Aminoethylphosphonic acid, D-Ala(P)

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About This Item

Linear Formula:

CH₃CH(NH₂)P(O)(OH)₂

CAS Number:

66068-76-6

Molecular Weight:

125.06

UNSPSC Code:

12352116

NACRES:

NA.22

PubChem Substance ID:

24862769

MDL number:

MFCD00066503

Beilstein/REAXYS Number:

4291033

Assay:

99%

Form:

solid

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Properties

Quality Segment

100

assay

99%

form

solid

optical activity

[α]20/D +4.8°, c = 5 in H₂O

mp

290 °C (dec.) (lit.)

functional group

amine

SMILES string

C[C@@H](N)P(O)(O)=O

InChI

1S/C2H8NO3P/c1-2(3)7(4,5)6/h2H,3H2,1H3,(H2,4,5,6)/t2-/m0/s1

InChI key

UIQSKEDQPSEGAU-REOHCLBHSA-N

Description

pictograms

GHS07

signalword

Warning

hcodes

H315,H319,H335

pcodes

P261 - P264 - P271 - P280 - P302 + P352 - P305 + P351 + P338

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number

MKBC7827

14508MX

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Spectra for FT-IR Raman

FT-NMR Spectra

Spectra - ATR-IR

Slow-binding and competitive inhibition of 8-amino-7-oxopelargonate synthase, a pyridoxal-5'-phosphate-dependent enzyme involved in biotin biosynthesis, by substrate and intermediate analogs. Kinetic and binding studies.

O Ploux et al.

European journal of biochemistry, 259(1-2), 63-70 (1999-01-23)

8-Amino-7-oxopelargonate synthase catalyzes the first committed step of biotin biosynthesis in micro-organisms and plants. Because inhibitors of this pathway might lead to antibacterials or herbicides, we have undertaken an inhibition study on 8-amino-7-oxopelargonate synthase using six different compounds. d-Alanine, the

[Kinetic characteristics and enantioselective action of penicillinase in the hydrolysis reaction of N-phenylacetyl derivatives of 1-aminoethylphosphonic acid and its esters].

D A Mironenko et al.

Biokhimiia (Moscow, Russia), 55(6), 1124-1131 (1990-06-01)

Penicillin acylase from E. coli (EC 3.5.1.11) was found to hydrolyze N-phenylacetylated 1-aminoethylphosphonic acid and its esters. The enzyme preferentially converts the R-form of the substrates: the ratios of the bimolecular rate constants of penicillin acylasecatalyzed hydrolysis of R- and

Inhibition of alanine racemase by alanine phosphonate: detection of an imine linkage to pyridoxal 5'-phosphate in the enzyme-inhibitor complex by solid-state 15N nuclear magnetic resonance.

V Copié et al.

Biochemistry, 27(14), 4966-4970 (1988-07-12)

Inhibition of alanine racemase from the Gram-positive bacterium Bacillus stearothermophilus by (1-aminoethyl) phosphonic acid (Ala-P) proceeds via a two-step reaction pathway in which reactivation occurs very slowly. In order to determine the mechanism of inhibition, we have recorded low-temperature, solid-state

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Global Trade Item Number

SKU	GTIN
367559-1G	04061826063071